Human Phenotype Ontology 
Grandparent Node:
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Abnormal myocardium morphology (HP:0001637)help
Parent Node:
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Cardiomyopathy (HP:0001638)help
..Starting node
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Dilated cardiomyopathy (HP:0001644)help
Term ID: 1644
Name: Dilated cardiomyopathy
Synonym: Cardiomyopathy, dilated; Congestive cardiomyopathy; DCM; Stretched and thinned heart muscle
Definition: Dilated cardiomyopathy (DCM) is defined by the presence of left ventricular dilatation and left ventricular systolic dysfunction in the absence of abnormal loading conditions (hypertension, valve disease) or coronary artery disease sufficient to cause global systolic impairment. Right ventricular dilation and dysfunction may be present but are not necessary for the diagnosis.
Comments:
Reference: HP:0001644
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAtrial cardiomyopathy (HP:0200127) help
..expandHistiocytoid cardiomyopathy (HP:0005152) help
..expandHypertrophic cardiomyopathy (HP:0001639) help
..expandNoncompaction cardiomyopathy (HP:0012817) help
..expandRestrictive cardiomyopathy (HP:0001723) help
..expandRight ventricular cardiomyopathy (HP:0011663) help
..expandTakotsubo cardiomyopathy (HP:0011665) help
InputHPO IDHPO termDistanceGeneGene id entrezDiseaseIdDiseaseNameDiseaseMIMConceptIDSourceTypical associationHGMD variantsClinVar variantsHGNC IDGeneMIM
 
HPO disease - gene - phenotype typical associations:
HP:0001644HP:0001644Dilated cardiomyopathy0ABCC9 CL E G H10060154Sandhaus Ben-Ami syndromeORPHA1104360601439
HP:0001644HP:0001644Dilated cardiomyopathy0ABCC9 CL E G H10060154Sandhaus Ben-Ami syndromeORPHA190960601439
HP:0001644HP:0001644Dilated cardiomyopathy0ACAD8 CL E G H27034611283Deficiency of isobutyryl-CoA dehydrogenase611283C1969809OMIM126987604773
HP:0001644HP:0001644Dilated cardiomyopathy0ACAD8 CL E G H27034611283Deficiency of isobutyryl-CoA dehydrogenase611283C1969809OMIM129187604773
HP:0001644HP:0001644Dilated cardiomyopathy0ACAD9 CL E G H2897699901ORPHA147821497611103
HP:0001644HP:0001644Dilated cardiomyopathy0ACAD9 CL E G H2897699901ORPHA142721497611103
HP:0001644HP:0001644Dilated cardiomyopathy0ACAD9 CL E G H28976611126Acyl-CoA dehydrogenase family, member 9, deficiency of611126C1970173OMIM147821497611103
HP:0001644HP:0001644Dilated cardiomyopathy0ACAD9 CL E G H28976611126Acyl-CoA dehydrogenase family, member 9, deficiency of611126C1970173OMIM142721497611103
HP:0001644HP:0001644Dilated cardiomyopathy0ACTA1 CL E G H58255310Congenital myopathy with fiber type disproportion255310C0546264OMIM1362129102610
HP:0001644HP:0001644Dilated cardiomyopathy0ACTA1 CL E G H58255310Congenital myopathy with fiber type disproportion255310C0546264OMIM1325129102610
HP:0001644HP:0001644Dilated cardiomyopathy0ACTC1 CL E G H70613424Dilated cardiomyopathy 1R613424C3150681OMIM1507143102540
HP:0001644HP:0001644Dilated cardiomyopathy0ACTC1 CL E G H70613424Dilated cardiomyopathy 1R613424C3150681OMIM1544143102540
HP:0001644HP:0001644Dilated cardiomyopathy0ACTC1 CL E G H70154Sandhaus Ben-Ami syndromeORPHA1544143102540
HP:0001644HP:0001644Dilated cardiomyopathy0ACTC1 CL E G H70154Sandhaus Ben-Ami syndromeORPHA1507143102540
HP:0001644HP:0001644Dilated cardiomyopathy0ACTN2 CL E G H88612158Dilated cardiomyopathy 1AA612158C2677338OMIM1973164102573
HP:0001644HP:0001644Dilated cardiomyopathy0ACTN2 CL E G H88612158Dilated cardiomyopathy 1AA612158C2677338OMIM1880164102573
HP:0001644HP:0001644Dilated cardiomyopathy0ACTN2 CL E G H88154Sandhaus Ben-Ami syndromeORPHA1973164102573
HP:0001644HP:0001644Dilated cardiomyopathy0ACTN2 CL E G H88154Sandhaus Ben-Ami syndromeORPHA1880164102573
HP:0001644HP:0001644Dilated cardiomyopathy0ALMS1 CL E G H784064ORPHA13342428606844
HP:0001644HP:0001644Dilated cardiomyopathy0ALMS1 CL E G H784064ORPHA12504428606844
HP:0001644HP:0001644Dilated cardiomyopathy0ALMS1 CL E G H7840203800Alstrom syndrome203800C0268425OMIM13342428606844
HP:0001644HP:0001644Dilated cardiomyopathy0ALMS1 CL E G H7840203800Alstrom syndrome203800C0268425OMIM12504428606844
HP:0001644HP:0001644Dilated cardiomyopathy0ANKRD1 CL E G H27063154Sandhaus Ben-Ami syndromeORPHA128415819609599
HP:0001644HP:0001644Dilated cardiomyopathy0ANKRD1 CL E G H27063154Sandhaus Ben-Ami syndromeORPHA125415819609599
HP:0001644HP:0001644Dilated cardiomyopathy0BAG3 CL E G H9531613881Dilated cardiomyopathy 1HH613881C3151293OMIM1603939603883
HP:0001644HP:0001644Dilated cardiomyopathy0BAG3 CL E G H9531613881Dilated cardiomyopathy 1HH613881C3151293OMIM1738939603883
HP:0001644HP:0001644Dilated cardiomyopathy0BAG3 CL E G H9531154Sandhaus Ben-Ami syndromeORPHA1738939603883
HP:0001644HP:0001644Dilated cardiomyopathy0BAG3 CL E G H9531154Sandhaus Ben-Ami syndromeORPHA1603939603883
HP:0001644HP:0001644Dilated cardiomyopathy0BOLA3 CL E G H388962614299Multiple mitochondrial dysfunctions syndrome 2614299C3280378OMIM17024415613183
HP:0001644HP:0001644Dilated cardiomyopathy0BOLA3 CL E G H388962614299Multiple mitochondrial dysfunctions syndrome 2614299C3280378OMIM16424415613183
HP:0001644HP:0001644Dilated cardiomyopathy0COX7B CL E G H13492556ORPHA11752291300885
HP:0001644HP:0001644Dilated cardiomyopathy0COX7B CL E G H13492556ORPHA11712291300885
HP:0001644HP:0001644Dilated cardiomyopathy0CPT2 CL E G H1376600649Carnitine palmitoyltransferase II deficiency, infantile600649C1833511OMIM15052330600650
HP:0001644HP:0001644Dilated cardiomyopathy0CPT2 CL E G H1376600649Carnitine palmitoyltransferase II deficiency, infantile600649C1833511OMIM16182330600650
HP:0001644HP:0001644Dilated cardiomyopathy0CPT2 CL E G H1376608836Carnitine palmitoyltransferase II deficiency, lethal neonatal608836C1833518OMIM16182330600650
HP:0001644HP:0001644Dilated cardiomyopathy0CPT2 CL E G H1376608836Carnitine palmitoyltransferase II deficiency, lethal neonatal608836C1833518OMIM15052330600650
HP:0001644HP:0001644Dilated cardiomyopathy0CRYAB CL E G H1410615184Dilated cardiomyopathy 1II615184C3554649OMIM12022389123590
HP:0001644HP:0001644Dilated cardiomyopathy0CRYAB CL E G H1410615184Dilated cardiomyopathy 1II615184C3554649OMIM11752389123590
HP:0001644HP:0001644Dilated cardiomyopathy0CRYAB CL E G H1410154Sandhaus Ben-Ami syndromeORPHA12022389123590
HP:0001644HP:0001644Dilated cardiomyopathy0CRYAB CL E G H1410154Sandhaus Ben-Ami syndromeORPHA11752389123590
HP:0001644HP:0001644Dilated cardiomyopathy0CSRP3 CL E G H8048607482Dilated cardiomyopathy 1M607482C1843808OMIM13192472600824
HP:0001644HP:0001644Dilated cardiomyopathy0CSRP3 CL E G H8048607482Dilated cardiomyopathy 1M607482C1843808OMIM12862472600824
HP:0001644HP:0001644Dilated cardiomyopathy0CSRP3 CL E G H8048154Sandhaus Ben-Ami syndromeORPHA13192472600824
HP:0001644HP:0001644Dilated cardiomyopathy0CSRP3 CL E G H8048154Sandhaus Ben-Ami syndromeORPHA12862472600824
HP:0001644HP:0001644Dilated cardiomyopathy0DES CL E G H1674604765Dilated cardiomyopathy 1I604765C1858154OMIM17032770125660
HP:0001644HP:0001644Dilated cardiomyopathy0DES CL E G H1674604765Dilated cardiomyopathy 1I604765C1858154OMIM16292770125660
HP:0001644HP:0001644Dilated cardiomyopathy0DES CL E G H1674154Sandhaus Ben-Ami syndromeORPHA17032770125660
HP:0001644HP:0001644Dilated cardiomyopathy0DES CL E G H1674154Sandhaus Ben-Ami syndromeORPHA16292770125660
HP:0001644HP:0001644Dilated cardiomyopathy0DMD CL E G H1756302045Dilated cardiomyopathy 3B302045C3668940OMIM163952928300377
HP:0001644HP:0001644Dilated cardiomyopathy0DMD CL E G H1756302045Dilated cardiomyopathy 3B302045C3668940OMIM156012928300377
HP:0001644HP:0001644Dilated cardiomyopathy0DMD CL E G H1756310200Duchenne muscular dystrophy310200C0013264OMIM163952928300377
HP:0001644HP:0001644Dilated cardiomyopathy0DMD CL E G H1756310200Duchenne muscular dystrophy310200C0013264OMIM156012928300377
HP:0001644HP:0001644Dilated cardiomyopathy0DMD CL E G H1756154Sandhaus Ben-Ami syndromeORPHA163952928300377
HP:0001644HP:0001644Dilated cardiomyopathy0DMD CL E G H1756154Sandhaus Ben-Ami syndromeORPHA156012928300377
HP:0001644HP:0001644Dilated cardiomyopathy0DNAJC19 CL E G H13111866634ORPHA19530528608977
HP:0001644HP:0001644Dilated cardiomyopathy0DNAJC19 CL E G H13111866634ORPHA17830528608977
HP:0001644HP:0001644Dilated cardiomyopathy0DNAJC19 CL E G H1311186101983-methylglutaconic aciduria type V610198C1857776OMIM17830528608977
HP:0001644HP:0001644Dilated cardiomyopathy0DNAJC19 CL E G H1311186101983-methylglutaconic aciduria type V610198C1857776OMIM19530528608977
HP:0001644HP:0001644Dilated cardiomyopathy0DOLK CL E G H22845610768Congenital disorder of glycosylation type 1M610768C1835849OMIM128623406610746
HP:0001644HP:0001644Dilated cardiomyopathy0DOLK CL E G H22845610768Congenital disorder of glycosylation type 1M610768C1835849OMIM135423406610746
HP:0001644HP:0001644Dilated cardiomyopathy0DOLK CL E G H22845154Sandhaus Ben-Ami syndromeORPHA135423406610746
HP:0001644HP:0001644Dilated cardiomyopathy0DOLK CL E G H22845154Sandhaus Ben-Ami syndromeORPHA128623406610746
HP:0001644HP:0001644Dilated cardiomyopathy0DPM3 CL E G H54344263494ORPHA1593007605951
HP:0001644HP:0001644Dilated cardiomyopathy0DPM3 CL E G H54344263494ORPHA1503007605951
HP:0001644HP:0001644Dilated cardiomyopathy0DPM3 CL E G H54344612937Congenital disorder of glycosylation type 1O612937C2752007OMIM1593007605951
HP:0001644HP:0001644Dilated cardiomyopathy0DPM3 CL E G H54344612937Congenital disorder of glycosylation type 1O612937C2752007OMIM1503007605951
HP:0001644HP:0001644Dilated cardiomyopathy0DSG2 CL E G H1829612877Dilated cardiomyopathy 1BB612877C2752072OMIM111143049125671
HP:0001644HP:0001644Dilated cardiomyopathy0DSG2 CL E G H1829612877Dilated cardiomyopathy 1BB612877C2752072OMIM112393049125671
HP:0001644HP:0001644Dilated cardiomyopathy0DSG2 CL E G H1829154Sandhaus Ben-Ami syndromeORPHA112393049125671
HP:0001644HP:0001644Dilated cardiomyopathy0DSG2 CL E G H1829154Sandhaus Ben-Ami syndromeORPHA111143049125671
HP:0001644HP:0001644Dilated cardiomyopathy0DSP CL E G H183265282ORPHA129983052125647
HP:0001644HP:0001644Dilated cardiomyopathy0DSP CL E G H183265282ORPHA126523052125647
HP:0001644HP:0001644Dilated cardiomyopathy0DSP CL E G H1832615821Cardiomyopathy, dilated, with woolly hair, keratoderma, and tooth agenesis615821C4014393OMIM126523052125647
HP:0001644HP:0001644Dilated cardiomyopathy0DSP CL E G H1832615821Cardiomyopathy, dilated, with woolly hair, keratoderma, and tooth agenesis615821C4014393OMIM129983052125647
HP:0001644HP:0001644Dilated cardiomyopathy0DSP CL E G H1832605676Dilated cardiomyopathy with woolly hair and keratoderma605676C1854063OMIM129983052125647
HP:0001644HP:0001644Dilated cardiomyopathy0DSP CL E G H1832605676Dilated cardiomyopathy with woolly hair and keratoderma605676C1854063OMIM126523052125647
HP:0001644HP:0001644Dilated cardiomyopathy0EPG5 CL E G H57724242840Vici syndrome242840C1855772OMIM1103329331615068
HP:0001644HP:0001644Dilated cardiomyopathy0EPG5 CL E G H57724242840Vici syndrome242840C1855772OMIM180129331615068
HP:0001644HP:0001644Dilated cardiomyopathy0EYA4 CL E G H2070217622ORPHA15623522603550
HP:0001644HP:0001644Dilated cardiomyopathy0EYA4 CL E G H2070217622ORPHA14763522603550
HP:0001644HP:0001644Dilated cardiomyopathy0EYA4 CL E G H2070605362Dilated cardiomyopathy 1J605362C1854368OMIM14763522603550
HP:0001644HP:0001644Dilated cardiomyopathy0EYA4 CL E G H2070605362Dilated cardiomyopathy 1J605362C1854368OMIM15623522603550
HP:0001644HP:0001644Dilated cardiomyopathy0FHL2 CL E G H2274154Sandhaus Ben-Ami syndromeORPHA11503703602633
HP:0001644HP:0001644Dilated cardiomyopathy0FHL2 CL E G H2274154Sandhaus Ben-Ami syndromeORPHA11303703602633
HP:0001644HP:0001644Dilated cardiomyopathy0FKRP CL E G H79147607155Limb-girdle muscular dystrophy-dystroglycanopathy, type C5607155C1846672OMIM157217997606596
HP:0001644HP:0001644Dilated cardiomyopathy0FKRP CL E G H79147607155Limb-girdle muscular dystrophy-dystroglycanopathy, type C5607155C1846672OMIM167117997606596
HP:0001644HP:0001644Dilated cardiomyopathy0FKTN CL E G H2218611615Dilated cardiomyopathy 1X611615C1969024OMIM15993622607440
HP:0001644HP:0001644Dilated cardiomyopathy0FKTN CL E G H2218611615Dilated cardiomyopathy 1X611615C1969024OMIM16793622607440
HP:0001644HP:0001644Dilated cardiomyopathy0FKTN CL E G H2218253800Fukuyama congenital muscular dystrophy253800C0410174OMIM16793622607440
HP:0001644HP:0001644Dilated cardiomyopathy0FKTN CL E G H2218253800Fukuyama congenital muscular dystrophy253800C0410174OMIM15993622607440
HP:0001644HP:0001644Dilated cardiomyopathy0FKTN CL E G H2218154Sandhaus Ben-Ami syndromeORPHA16793622607440
HP:0001644HP:0001644Dilated cardiomyopathy0FKTN CL E G H2218154Sandhaus Ben-Ami syndromeORPHA15993622607440
HP:0001644HP:0001644Dilated cardiomyopathy0GATAD1 CL E G H57798614672Cardiomyopathy, dilated, 2b614672C3553409OMIM133229941614518
HP:0001644HP:0001644Dilated cardiomyopathy0GATAD1 CL E G H57798614672Cardiomyopathy, dilated, 2b614672C3553409OMIM138429941614518
HP:0001644HP:0001644Dilated cardiomyopathy0GATAD1 CL E G H57798154Sandhaus Ben-Ami syndromeORPHA138429941614518
HP:0001644HP:0001644Dilated cardiomyopathy0GATAD1 CL E G H57798154Sandhaus Ben-Ami syndromeORPHA133229941614518
HP:0001644HP:0001644Dilated cardiomyopathy0GLB1 CL E G H2720230500Infantile GM1 gangliosidosis230500C0268271OMIM15964298611458
HP:0001644HP:0001644Dilated cardiomyopathy0GLB1 CL E G H2720230500Infantile GM1 gangliosidosis230500C0268271OMIM15074298611458
HP:0001644HP:0001644Dilated cardiomyopathy0HADH CL E G H3033231530Deficiency of 3-hydroxyacyl-CoA dehydrogenase231530C1291230OMIM11564799601609
HP:0001644HP:0001644Dilated cardiomyopathy0HADH CL E G H3033231530Deficiency of 3-hydroxyacyl-CoA dehydrogenase231530C1291230OMIM11374799601609
HP:0001644HP:0001644Dilated cardiomyopathy0HADHA CL E G H3030609015Mitochondrial trifunctional protein deficiency609015C0342786OMIM14774801600890
HP:0001644HP:0001644Dilated cardiomyopathy0HADHA CL E G H3030609015Mitochondrial trifunctional protein deficiency609015C0342786OMIM15274801600890
HP:0001644HP:0001644Dilated cardiomyopathy0HADHB CL E G H3032609015Mitochondrial trifunctional protein deficiency609015C0342786OMIM12424803143450
HP:0001644HP:0001644Dilated cardiomyopathy0HADHB CL E G H3032609015Mitochondrial trifunctional protein deficiency609015C0342786OMIM12134803143450
HP:0001644HP:0001644Dilated cardiomyopathy0HAMP CL E G H5781779230ORPHA16115598606464
HP:0001644HP:0001644Dilated cardiomyopathy0HAMP CL E G H5781779230ORPHA15215598606464
HP:0001644HP:0001644Dilated cardiomyopathy0HCCS CL E G H30522556ORPHA12204837300056
HP:0001644HP:0001644Dilated cardiomyopathy0HCCS CL E G H30522556ORPHA12144837300056
HP:0001644HP:0001644Dilated cardiomyopathy0HJV CL E G H14873879230ORPHA13694887608374
HP:0001644HP:0001644Dilated cardiomyopathy0HJV CL E G H14873879230ORPHA13384887608374
HP:0001644HP:0001644Dilated cardiomyopathy0HJV CL E G H148738602390Hemochromatosis type 2A602390C1865614OMIM13384887608374
HP:0001644HP:0001644Dilated cardiomyopathy0HJV CL E G H148738602390Hemochromatosis type 2A602390C1865614OMIM13694887608374
HP:0001644HP:0001644Dilated cardiomyopathy0JUP CL E G H3728601214Naxos disease601214C1832600OMIM16396207173325
HP:0001644HP:0001644Dilated cardiomyopathy0JUP CL E G H3728601214Naxos disease601214C1832600OMIM17456207173325
HP:0001644HP:0001644Dilated cardiomyopathy0KAT6B CL E G H23522603736Young Simpson syndrome603736C1863557OMIM139617582605880
HP:0001644HP:0001644Dilated cardiomyopathy0KAT6B CL E G H23522603736Young Simpson syndrome603736C1863557OMIM148717582605880
HP:0001644HP:0001644Dilated cardiomyopathy0LAMA4 CL E G H3910615235Dilated cardiomyopathy 1JJ615235C3808935OMIM19046484600133
HP:0001644HP:0001644Dilated cardiomyopathy0LAMA4 CL E G H3910615235Dilated cardiomyopathy 1JJ615235C3808935OMIM110276484600133
HP:0001644HP:0001644Dilated cardiomyopathy0LAMA4 CL E G H3910154Sandhaus Ben-Ami syndromeORPHA110276484600133
HP:0001644HP:0001644Dilated cardiomyopathy0LAMA4 CL E G H3910154Sandhaus Ben-Ami syndromeORPHA19046484600133
HP:0001644HP:0001644Dilated cardiomyopathy0LAMP2 CL E G H392034587ORPHA17266501309060
HP:0001644HP:0001644Dilated cardiomyopathy0LAMP2 CL E G H392034587ORPHA16726501309060
HP:0001644HP:0001644Dilated cardiomyopathy0LAMP2 CL E G H3920300257Danon disease300257C0878677OMIM17266501309060
HP:0001644HP:0001644Dilated cardiomyopathy0LAMP2 CL E G H3920300257Danon disease300257C0878677OMIM16726501309060
HP:0001644HP:0001644Dilated cardiomyopathy0LDB3 CL E G H11155601493Dilated cardiomyopathy 1C601493C1832244OMIM179615710605906
HP:0001644HP:0001644Dilated cardiomyopathy0LDB3 CL E G H11155601493Dilated cardiomyopathy 1C601493C1832244OMIM188815710605906
HP:0001644HP:0001644Dilated cardiomyopathy0LDB3 CL E G H11155154Sandhaus Ben-Ami syndromeORPHA188815710605906
HP:0001644HP:0001644Dilated cardiomyopathy0LDB3 CL E G H11155154Sandhaus Ben-Ami syndromeORPHA179615710605906
HP:0001644HP:0001644Dilated cardiomyopathy0LIMS2 CL E G H55679616827Muscular dystrophy, limb-girdle, type 2W616827C4225192OMIM116616084607908
HP:0001644HP:0001644Dilated cardiomyopathy0LIMS2 CL E G H55679616827Muscular dystrophy, limb-girdle, type 2W616827C4225192OMIM119616084607908
HP:0001644HP:0001644Dilated cardiomyopathy0LMNA CL E G H400098855ORPHA114866636150330
HP:0001644HP:0001644Dilated cardiomyopathy0LMNA CL E G H4000168796ORPHA114866636150330
HP:0001644HP:0001644Dilated cardiomyopathy0LMNA CL E G H400098855ORPHA113476636150330
HP:0001644HP:0001644Dilated cardiomyopathy0LMNA CL E G H4000168796ORPHA113476636150330
HP:0001644HP:0001644Dilated cardiomyopathy0LMNA CL E G H40002229ORPHA114866636150330
HP:0001644HP:0001644Dilated cardiomyopathy0LMNA CL E G H40002229ORPHA113476636150330
HP:0001644HP:0001644Dilated cardiomyopathy0LMNA CL E G H4000181350Benign scapuloperoneal muscular dystrophy with cardiomyopathy181350C0410190OMIM114866636150330
HP:0001644HP:0001644Dilated cardiomyopathy0LMNA CL E G H4000181350Benign scapuloperoneal muscular dystrophy with cardiomyopathy181350C0410190OMIM113476636150330
HP:0001644HP:0001644Dilated cardiomyopathy0LMNA CL E G H4000115200Dilated cardiomyopathy 1A115200C1449563OMIM114866636150330
HP:0001644HP:0001644Dilated cardiomyopathy0LMNA CL E G H4000115200Dilated cardiomyopathy 1A115200C1449563OMIM113476636150330
HP:0001644HP:0001644Dilated cardiomyopathy0LMNA CL E G H4000212112Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome212112C0796031OMIM114866636150330
HP:0001644HP:0001644Dilated cardiomyopathy0LMNA CL E G H4000212112Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome212112C0796031OMIM113476636150330
HP:0001644HP:0001644Dilated cardiomyopathy0LMNA CL E G H4000610140Heart-hand syndrome, Slovenian type610140C1857829OMIM114866636150330
HP:0001644HP:0001644Dilated cardiomyopathy0LMNA CL E G H4000610140Heart-hand syndrome, Slovenian type610140C1857829OMIM113476636150330
HP:0001644HP:0001644Dilated cardiomyopathy0MGME1 CL E G H92667352447ORPHA17516205615076
HP:0001644HP:0001644Dilated cardiomyopathy0MGME1 CL E G H92667352447ORPHA16916205615076
HP:0001644HP:0001644Dilated cardiomyopathy0MT-TK CL E G H45661349Chromosome 9, partial monosomy 9pC2931695ORPHA17489590060
HP:0001644HP:0001644Dilated cardiomyopathy0MYBPC3 CL E G H4607615396Left ventricular noncompaction 10615396C3715165OMIM126947551600958
HP:0001644HP:0001644Dilated cardiomyopathy0MYBPC3 CL E G H4607615396Left ventricular noncompaction 10615396C3715165OMIM124447551600958
HP:0001644HP:0001644Dilated cardiomyopathy0MYBPC3 CL E G H4607154Sandhaus Ben-Ami syndromeORPHA126947551600958
HP:0001644HP:0001644Dilated cardiomyopathy0MYBPC3 CL E G H4607154Sandhaus Ben-Ami syndromeORPHA124447551600958
HP:0001644HP:0001644Dilated cardiomyopathy0MYH6 CL E G H4624613252Dilated cardiomyopathy 1EE613252C2750466OMIM112337576160710
HP:0001644HP:0001644Dilated cardiomyopathy0MYH6 CL E G H4624613252Dilated cardiomyopathy 1EE613252C2750466OMIM113877576160710
HP:0001644HP:0001644Dilated cardiomyopathy0MYH6 CL E G H4624154Sandhaus Ben-Ami syndromeORPHA113877576160710
HP:0001644HP:0001644Dilated cardiomyopathy0MYH6 CL E G H4624154Sandhaus Ben-Ami syndromeORPHA112337576160710
HP:0001644HP:0001644Dilated cardiomyopathy0MYH7 CL E G H4625255310Congenital myopathy with fiber type disproportion255310C0546264OMIM132927577160760
HP:0001644HP:0001644Dilated cardiomyopathy0MYH7 CL E G H4625255310Congenital myopathy with fiber type disproportion255310C0546264OMIM129607577160760
HP:0001644HP:0001644Dilated cardiomyopathy0MYH7 CL E G H4625613426Dilated cardiomyopathy 1S613426C1834481OMIM132927577160760
HP:0001644HP:0001644Dilated cardiomyopathy0MYH7 CL E G H4625613426Dilated cardiomyopathy 1S613426C1834481OMIM129607577160760
HP:0001644HP:0001644Dilated cardiomyopathy0MYH7 CL E G H4625255160Myopathy, myosin storage, autosomal recessive255160C1850709OMIM132927577160760
HP:0001644HP:0001644Dilated cardiomyopathy0MYH7 CL E G H4625255160Myopathy, myosin storage, autosomal recessive255160C1850709OMIM129607577160760
HP:0001644HP:0001644Dilated cardiomyopathy0MYH7 CL E G H4625154Sandhaus Ben-Ami syndromeORPHA132927577160760
HP:0001644HP:0001644Dilated cardiomyopathy0MYH7 CL E G H4625154Sandhaus Ben-Ami syndromeORPHA129607577160760
HP:0001644HP:0001644Dilated cardiomyopathy0MYPN CL E G H84665154Sandhaus Ben-Ami syndromeORPHA1103323246608517
HP:0001644HP:0001644Dilated cardiomyopathy0MYPN CL E G H84665154Sandhaus Ben-Ami syndromeORPHA188723246608517
HP:0001644HP:0001644Dilated cardiomyopathy0NDUFB11 CL E G H545392556ORPHA118320372300403
HP:0001644HP:0001644Dilated cardiomyopathy0NDUFB11 CL E G H545392556ORPHA117720372300403
HP:0001644HP:0001644Dilated cardiomyopathy0NDUFB11 CL E G H54539300952Linear skin defects with multiple congenital anomalies 3300952C4225421OMIM118320372300403
HP:0001644HP:0001644Dilated cardiomyopathy0NDUFB11 CL E G H54539300952Linear skin defects with multiple congenital anomalies 3300952C4225421OMIM117720372300403
HP:0001644HP:0001644Dilated cardiomyopathy0NEBL CL E G H10529154Sandhaus Ben-Ami syndromeORPHA166416932605491
HP:0001644HP:0001644Dilated cardiomyopathy0NEBL CL E G H10529154Sandhaus Ben-Ami syndromeORPHA157716932605491
HP:0001644HP:0001644Dilated cardiomyopathy0NEXN CL E G H91624613122Dilated cardiomyopathy 1CC613122C2751084OMIM139529557613121
HP:0001644HP:0001644Dilated cardiomyopathy0NEXN CL E G H91624613122Dilated cardiomyopathy 1CC613122C2751084OMIM143529557613121
HP:0001644HP:0001644Dilated cardiomyopathy0NEXN CL E G H91624154Sandhaus Ben-Ami syndromeORPHA143529557613121
HP:0001644HP:0001644Dilated cardiomyopathy0NEXN CL E G H91624154Sandhaus Ben-Ami syndromeORPHA139529557613121
HP:0001644HP:0001644Dilated cardiomyopathy0PGM1 CL E G H5236614921Congenital disorder of glycosylation type 1t614921C2752015OMIM12608905171900
HP:0001644HP:0001644Dilated cardiomyopathy0PGM1 CL E G H5236614921Congenital disorder of glycosylation type 1t614921C2752015OMIM12328905171900
HP:0001644HP:0001644Dilated cardiomyopathy0PLN CL E G H5350609909Dilated cardiomyopathy 1P609909C1835928OMIM11439080172405
HP:0001644HP:0001644Dilated cardiomyopathy0PLN CL E G H5350609909Dilated cardiomyopathy 1P609909C1835928OMIM11529080172405
HP:0001644HP:0001644Dilated cardiomyopathy0PLN CL E G H5350154Sandhaus Ben-Ami syndromeORPHA11529080172405
HP:0001644HP:0001644Dilated cardiomyopathy0PLN CL E G H5350154Sandhaus Ben-Ami syndromeORPHA11439080172405
HP:0001644HP:0001644Dilated cardiomyopathy0POLG CL E G H5428607459Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis607459C1843851OMIM117129179174763
HP:0001644HP:0001644Dilated cardiomyopathy0POLG CL E G H5428607459Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis607459C1843851OMIM114709179174763
HP:0001644HP:0001644Dilated cardiomyopathy0PPCS CL E G H79717618189CARDIOMYOPATHY, DILATED, 2C618189OMIM12025686609853
HP:0001644HP:0001644Dilated cardiomyopathy0PPCS CL E G H79717618189CARDIOMYOPATHY, DILATED, 2C618189OMIM17925686609853
HP:0001644HP:0001644Dilated cardiomyopathy0PPCS CL E G H79717154Sandhaus Ben-Ami syndromeORPHA17925686609853
HP:0001644HP:0001644Dilated cardiomyopathy0PPCS CL E G H79717154Sandhaus Ben-Ami syndromeORPHA12025686609853
HP:0001644HP:0001644Dilated cardiomyopathy0PRDM16 CL E G H63976615373Left ventricular noncompaction 8615373C3809288OMIM188614000605557
HP:0001644HP:0001644Dilated cardiomyopathy0PRDM16 CL E G H63976615373Left ventricular noncompaction 8615373C3809288OMIM198614000605557
HP:0001644HP:0001644Dilated cardiomyopathy0PRDM16 CL E G H63976154Sandhaus Ben-Ami syndromeORPHA198614000605557
HP:0001644HP:0001644Dilated cardiomyopathy0PRDM16 CL E G H63976154Sandhaus Ben-Ami syndromeORPHA188614000605557
HP:0001644HP:0001644Dilated cardiomyopathy0PSEN1 CL E G H5663613694Cardiomyopathy, dilated, 1u613694C3160720OMIM14319508104311
HP:0001644HP:0001644Dilated cardiomyopathy0PSEN1 CL E G H5663613694Cardiomyopathy, dilated, 1u613694C3160720OMIM14089508104311
HP:0001644HP:0001644Dilated cardiomyopathy0PSEN1 CL E G H5663154Sandhaus Ben-Ami syndromeORPHA14319508104311
HP:0001644HP:0001644Dilated cardiomyopathy0PSEN1 CL E G H5663154Sandhaus Ben-Ami syndromeORPHA14089508104311
HP:0001644HP:0001644Dilated cardiomyopathy0PSEN2 CL E G H5664613697Dilated cardiomyopathy 1V613697C3150958OMIM12039509600759
HP:0001644HP:0001644Dilated cardiomyopathy0PSEN2 CL E G H5664613697Dilated cardiomyopathy 1V613697C3150958OMIM12169509600759
HP:0001644HP:0001644Dilated cardiomyopathy0PSEN2 CL E G H5664154Sandhaus Ben-Ami syndromeORPHA12169509600759
HP:0001644HP:0001644Dilated cardiomyopathy0PSEN2 CL E G H5664154Sandhaus Ben-Ami syndromeORPHA12039509600759
HP:0001644HP:0001644Dilated cardiomyopathy0RAF1 CL E G H5894615916Cardiomyopathy, dilated, 1NN615916C4014656OMIM16259829164760
HP:0001644HP:0001644Dilated cardiomyopathy0RAF1 CL E G H5894615916Cardiomyopathy, dilated, 1NN615916C4014656OMIM16909829164760
HP:0001644HP:0001644Dilated cardiomyopathy0RAF1 CL E G H5894154Sandhaus Ben-Ami syndromeORPHA16909829164760
HP:0001644HP:0001644Dilated cardiomyopathy0RAF1 CL E G H5894154Sandhaus Ben-Ami syndromeORPHA16259829164760
HP:0001644HP:0001644Dilated cardiomyopathy0RBCK1 CL E G H10616615895Polyglucosan body myopathy 1 with or without immunodeficiency615895C4014605OMIM131215864610924
HP:0001644HP:0001644Dilated cardiomyopathy0RBCK1 CL E G H10616615895Polyglucosan body myopathy 1 with or without immunodeficiency615895C4014605OMIM126315864610924
HP:0001644HP:0001644Dilated cardiomyopathy0RBM20 CL E G H282996613172Dilated cardiomyopathy 1DD613172C2750995OMIM1117727424613171
HP:0001644HP:0001644Dilated cardiomyopathy0RBM20 CL E G H282996613172Dilated cardiomyopathy 1DD613172C2750995OMIM1102427424613171
HP:0001644HP:0001644Dilated cardiomyopathy0RBM20 CL E G H282996154Sandhaus Ben-Ami syndromeORPHA1117727424613171
HP:0001644HP:0001644Dilated cardiomyopathy0RBM20 CL E G H282996154Sandhaus Ben-Ami syndromeORPHA1102427424613171
HP:0001644HP:0001644Dilated cardiomyopathy0RYR1 CL E G H6261255310Congenital myopathy with fiber type disproportion255310C0546264OMIM1460410483180901
HP:0001644HP:0001644Dilated cardiomyopathy0RYR1 CL E G H6261255310Congenital myopathy with fiber type disproportion255310C0546264OMIM1410110483180901
HP:0001644HP:0001644Dilated cardiomyopathy0SCN5A CL E G H6331601154Dilated cardiomyopathy 1E601154C1832680OMIM1286110593600163
HP:0001644HP:0001644Dilated cardiomyopathy0SCN5A CL E G H6331601154Dilated cardiomyopathy 1E601154C1832680OMIM1262410593600163
HP:0001644HP:0001644Dilated cardiomyopathy0SCN5A CL E G H6331154Sandhaus Ben-Ami syndromeORPHA1286110593600163
HP:0001644HP:0001644Dilated cardiomyopathy0SCN5A CL E G H6331154Sandhaus Ben-Ami syndromeORPHA1262410593600163
HP:0001644HP:0001644Dilated cardiomyopathy0SDHA CL E G H6389613642Dilated cardiomyopathy 1GG613642C3150898OMIM1154510680600857
HP:0001644HP:0001644Dilated cardiomyopathy0SDHA CL E G H6389613642Dilated cardiomyopathy 1GG613642C3150898OMIM1177810680600857
HP:0001644HP:0001644Dilated cardiomyopathy0SDHA CL E G H6389252011Mitochondrial complex II deficiency252011C1855008OMIM1177810680600857
HP:0001644HP:0001644Dilated cardiomyopathy0SDHA CL E G H6389252011Mitochondrial complex II deficiency252011C1855008OMIM1154510680600857
HP:0001644HP:0001644Dilated cardiomyopathy0SDHA CL E G H6389154Sandhaus Ben-Ami syndromeORPHA1177810680600857
HP:0001644HP:0001644Dilated cardiomyopathy0SDHA CL E G H6389154Sandhaus Ben-Ami syndromeORPHA1154510680600857
HP:0001644HP:0001644Dilated cardiomyopathy0SDHAF1 CL E G H644096252011Mitochondrial complex II deficiency252011C1855008OMIM15433867612848
HP:0001644HP:0001644Dilated cardiomyopathy0SDHAF1 CL E G H644096252011Mitochondrial complex II deficiency252011C1855008OMIM14633867612848
HP:0001644HP:0001644Dilated cardiomyopathy0SDHD CL E G H6392252011Mitochondrial complex II deficiency252011C1855008OMIM150710683602690
HP:0001644HP:0001644Dilated cardiomyopathy0SDHD CL E G H6392252011Mitochondrial complex II deficiency252011C1855008OMIM144210683602690
HP:0001644HP:0001644Dilated cardiomyopathy0SELENON CL E G H57190255310Congenital myopathy with fiber type disproportion255310C0546264OMIM150515999606210
HP:0001644HP:0001644Dilated cardiomyopathy0SELENON CL E G H57190255310Congenital myopathy with fiber type disproportion255310C0546264OMIM145415999606210
HP:0001644HP:0001644Dilated cardiomyopathy0SGCD CL E G H6444606685Dilated cardiomyopathy 1L606685C1847667OMIM151010807601411
HP:0001644HP:0001644Dilated cardiomyopathy0SGCD CL E G H6444606685Dilated cardiomyopathy 1L606685C1847667OMIM154610807601411
HP:0001644HP:0001644Dilated cardiomyopathy0SGCD CL E G H6444154Sandhaus Ben-Ami syndromeORPHA154610807601411
HP:0001644HP:0001644Dilated cardiomyopathy0SGCD CL E G H6444154Sandhaus Ben-Ami syndromeORPHA151010807601411
HP:0001644HP:0001644Dilated cardiomyopathy0SPEG CL E G H10290615959Myopathy, centronuclear, 5615959C4014814OMIM163716901615950
HP:0001644HP:0001644Dilated cardiomyopathy0SPEG CL E G H10290615959Myopathy, centronuclear, 5615959C4014814OMIM126516901615950
HP:0001644HP:0001644Dilated cardiomyopathy0TAF1A CL E G H9015154Sandhaus Ben-Ami syndromeORPHA13011532604903
HP:0001644HP:0001644Dilated cardiomyopathy0TAF1A CL E G H9015154Sandhaus Ben-Ami syndromeORPHA12911532604903
HP:0001644HP:0001644Dilated cardiomyopathy0TAZ CL E G H69013020603-Methylglutaconic aciduria type 2302060C0574083OMIM111577300394
HP:0001644HP:0001644Dilated cardiomyopathy0TAZ CL E G H6901111Recurrent respiratory papillomatosisORPHA111577300394
HP:0001644HP:0001644Dilated cardiomyopathy0TAZ CL E G H6901154Sandhaus Ben-Ami syndromeORPHA111577300394
HP:0001644HP:0001644Dilated cardiomyopathy0TCAP CL E G H8557607487Dilated cardiomyopathy 1N607487C1843791OMIM120011610604488
HP:0001644HP:0001644Dilated cardiomyopathy0TCAP CL E G H8557607487Dilated cardiomyopathy 1N607487C1843791OMIM122611610604488
HP:0001644HP:0001644Dilated cardiomyopathy0TCAP CL E G H8557154Sandhaus Ben-Ami syndromeORPHA120011610604488
HP:0001644HP:0001644Dilated cardiomyopathy0TCAP CL E G H8557154Sandhaus Ben-Ami syndromeORPHA122611610604488
HP:0001644HP:0001644Dilated cardiomyopathy0TMPO CL E G H7112154Sandhaus Ben-Ami syndromeORPHA137311875188380
HP:0001644HP:0001644Dilated cardiomyopathy0TMPO CL E G H7112154Sandhaus Ben-Ami syndromeORPHA133111875188380
HP:0001644HP:0001644Dilated cardiomyopathy0TNNC1 CL E G H7134611879Dilated cardiomyopathy 1Z611879C2678475OMIM120711943191040
HP:0001644HP:0001644Dilated cardiomyopathy0TNNC1 CL E G H7134611879Dilated cardiomyopathy 1Z611879C2678475OMIM118511943191040
HP:0001644HP:0001644Dilated cardiomyopathy0TNNC1 CL E G H7134154Sandhaus Ben-Ami syndromeORPHA118511943191040
HP:0001644HP:0001644Dilated cardiomyopathy0TNNC1 CL E G H7134154Sandhaus Ben-Ami syndromeORPHA120711943191040
HP:0001644HP:0001644Dilated cardiomyopathy0TNNI3 CL E G H7137613286Dilated cardiomyopathy 1FF613286C2750091OMIM153911947191044
HP:0001644HP:0001644Dilated cardiomyopathy0TNNI3 CL E G H7137613286Dilated cardiomyopathy 1FF613286C2750091OMIM149611947191044
HP:0001644HP:0001644Dilated cardiomyopathy0TNNI3 CL E G H7137611880Dilated cardiomyopathy 2A611880C2678474OMIM149611947191044
HP:0001644HP:0001644Dilated cardiomyopathy0TNNI3 CL E G H7137611880Dilated cardiomyopathy 2A611880C2678474OMIM153911947191044
HP:0001644HP:0001644Dilated cardiomyopathy0TNNI3 CL E G H7137154Sandhaus Ben-Ami syndromeORPHA153911947191044
HP:0001644HP:0001644Dilated cardiomyopathy0TNNI3 CL E G H7137154Sandhaus Ben-Ami syndromeORPHA149611947191044
HP:0001644HP:0001644Dilated cardiomyopathy0TNNI3K CL E G H51086616117Cardiac conduction disease with or without dilated cardiomyopathy616117C4015285OMIM136319661613932
HP:0001644HP:0001644Dilated cardiomyopathy0TNNI3K CL E G H51086616117Cardiac conduction disease with or without dilated cardiomyopathy616117C4015285OMIM112719661613932
HP:0001644HP:0001644Dilated cardiomyopathy0TNNT2 CL E G H7139601494Left ventricular noncompaction 6601494C1832243OMIM165911949191045
HP:0001644HP:0001644Dilated cardiomyopathy0TNNT2 CL E G H7139601494Left ventricular noncompaction 6601494C1832243OMIM161111949191045
HP:0001644HP:0001644Dilated cardiomyopathy0TNNT2 CL E G H7139154Sandhaus Ben-Ami syndromeORPHA161111949191045
HP:0001644HP:0001644Dilated cardiomyopathy0TNNT2 CL E G H7139154Sandhaus Ben-Ami syndromeORPHA165911949191045
HP:0001644HP:0001644Dilated cardiomyopathy0TPM1 CL E G H7168611878Dilated cardiomyopathy 1Y611878C2678476OMIM158512010191010
HP:0001644HP:0001644Dilated cardiomyopathy0TPM1 CL E G H7168611878Dilated cardiomyopathy 1Y611878C2678476OMIM163212010191010
HP:0001644HP:0001644Dilated cardiomyopathy0TPM1 CL E G H7168154Sandhaus Ben-Ami syndromeORPHA163212010191010
HP:0001644HP:0001644Dilated cardiomyopathy0TPM1 CL E G H7168154Sandhaus Ben-Ami syndromeORPHA158512010191010
HP:0001644HP:0001644Dilated cardiomyopathy0TPM2 CL E G H7169255310Congenital myopathy with fiber type disproportion255310C0546264OMIM124212011190990
HP:0001644HP:0001644Dilated cardiomyopathy0TPM2 CL E G H7169255310Congenital myopathy with fiber type disproportion255310C0546264OMIM123412011190990
HP:0001644HP:0001644Dilated cardiomyopathy0TPM3 CL E G H7170255310Congenital myopathy with fiber type disproportion255310C0546264OMIM128312012191030
HP:0001644HP:0001644Dilated cardiomyopathy0TPM3 CL E G H7170255310Congenital myopathy with fiber type disproportion255310C0546264OMIM126112012191030
HP:0001644HP:0001644Dilated cardiomyopathy0TTN CL E G H7273604145Dilated cardiomyopathy 1G604145C1858763OMIM11902812403188840
HP:0001644HP:0001644Dilated cardiomyopathy0TTN CL E G H7273604145Dilated cardiomyopathy 1G604145C1858763OMIM11798412403188840
HP:0001644HP:0001644Dilated cardiomyopathy0TTN CL E G H7273613765Familial hypertrophic cardiomyopathy 9613765C1861065OMIM11902812403188840
HP:0001644HP:0001644Dilated cardiomyopathy0TTN CL E G H7273613765Familial hypertrophic cardiomyopathy 9613765C1861065OMIM11798412403188840
HP:0001644HP:0001644Dilated cardiomyopathy0TTN CL E G H7273611705Myopathy, early-onset, with fatal cardiomyopathy611705C2673677OMIM11902812403188840
HP:0001644HP:0001644Dilated cardiomyopathy0TTN CL E G H7273611705Myopathy, early-onset, with fatal cardiomyopathy611705C2673677OMIM11798412403188840
HP:0001644HP:0001644Dilated cardiomyopathy0TTN CL E G H7273154Sandhaus Ben-Ami syndromeORPHA11798412403188840
HP:0001644HP:0001644Dilated cardiomyopathy0TTN CL E G H7273154Sandhaus Ben-Ami syndromeORPHA11902812403188840
HP:0001644HP:0001644Dilated cardiomyopathy0TWNK CL E G H56652607459Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis607459C1843851OMIM12341160606075
HP:0001644HP:0001644Dilated cardiomyopathy0TWNK CL E G H56652607459Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis607459C1843851OMIM12701160606075
HP:0001644HP:0001644Dilated cardiomyopathy0TXNRD2 CL E G H10587154Sandhaus Ben-Ami syndromeORPHA182218155606448
HP:0001644HP:0001644Dilated cardiomyopathy0TXNRD2 CL E G H10587154Sandhaus Ben-Ami syndromeORPHA176518155606448
HP:0001644HP:0001644Dilated cardiomyopathy0VCL CL E G H7414611407Dilated cardiomyopathy 1W611407C1969639OMIM179712665193065
HP:0001644HP:0001644Dilated cardiomyopathy0VCL CL E G H7414611407Dilated cardiomyopathy 1W611407C1969639OMIM170712665193065
HP:0001644HP:0001644Dilated cardiomyopathy0VCL CL E G H7414154Sandhaus Ben-Ami syndromeORPHA170712665193065
HP:0001644HP:0001644Dilated cardiomyopathy0VCL CL E G H7414154Sandhaus Ben-Ami syndromeORPHA179712665193065
HP:0001644HP:0001644Dilated cardiomyopathy0XK CL E G H7504300842McLeod neuroacanthocytosis syndrome300842C0398568OMIM119512811314850
HP:0001644HP:0001644Dilated cardiomyopathy0XK CL E G H7504300842McLeod neuroacanthocytosis syndrome300842C0398568OMIM119012811314850
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0001644HP:0001644Dilated cardiomyopathy0ABCC9 CL E G H10060608569Dilated cardiomyopathy 1O608569C1837839OMIM090960601439
HP:0001644HP:0001644Dilated cardiomyopathy0ABCC9 CL E G H10060608569Dilated cardiomyopathy 1O608569C1837839OMIM0104360601439
HP:0001644HP:0001644Dilated cardiomyopathy0ACTA1 CL E G H582020ORPHA0362129102610
HP:0001644HP:0001644Dilated cardiomyopathy0ACTA1 CL E G H582020ORPHA0325129102610
HP:0001644HP:0001644Dilated cardiomyopathy0ACTA1 CL E G H58161800Nemaline myopathy 3161800C3711389OMIM0362129102610
HP:0001644HP:0001644Dilated cardiomyopathy0ACTA1 CL E G H58161800Nemaline myopathy 3161800C3711389OMIM0325129102610
HP:0001644HP:0001644Dilated cardiomyopathy0ADCY5 CL E G H111324588ORPHA0365236600293
HP:0001644HP:0001644Dilated cardiomyopathy0ADCY5 CL E G H111324588ORPHA0293236600293
HP:0001644HP:0001644Dilated cardiomyopathy0ADCY5 CL E G H111606703Dyskinesia, familial, with facial myokymia606703C1847627OMIM0365236600293
HP:0001644HP:0001644Dilated cardiomyopathy0ADCY5 CL E G H111606703Dyskinesia, familial, with facial myokymia606703C1847627OMIM0293236600293
HP:0001644HP:0001644Dilated cardiomyopathy0ANKRD11 CL E G H2912326125016q24.3 microdeletion syndromeCN202174ORPHA0118421316611192
HP:0001644HP:0001644Dilated cardiomyopathy0ANKRD11 CL E G H2912326125016q24.3 microdeletion syndromeCN202174ORPHA0110121316611192
HP:0001644HP:0001644Dilated cardiomyopathy0BBS2 CL E G H583615981Bardet-Biedl syndrome 2615981C2936863OMIM0482967606151
HP:0001644HP:0001644Dilated cardiomyopathy0BBS2 CL E G H583615981Bardet-Biedl syndrome 2615981C2936863OMIM0585967606151
HP:0001644HP:0001644Dilated cardiomyopathy0CHKB CL E G H1120602541Muscular dystrophy, congenital, megaconial type602541C1865233OMIM03821938612395
HP:0001644HP:0001644Dilated cardiomyopathy0CHKB CL E G H1120602541Muscular dystrophy, congenital, megaconial type602541C1865233OMIM03351938612395
HP:0001644HP:0001644Dilated cardiomyopathy0COL7A1 CL E G H129479409ORPHA020282214120120
HP:0001644HP:0001644Dilated cardiomyopathy0COL7A1 CL E G H129479408ORPHA020282214120120
HP:0001644HP:0001644Dilated cardiomyopathy0COL7A1 CL E G H129479409ORPHA016582214120120
HP:0001644HP:0001644Dilated cardiomyopathy0COL7A1 CL E G H129479408ORPHA016582214120120
HP:0001644HP:0001644Dilated cardiomyopathy0DES CL E G H1674601419Myofibrillar myopathy 1601419C1832370OMIM07032770125660
HP:0001644HP:0001644Dilated cardiomyopathy0DES CL E G H1674601419Myofibrillar myopathy 1601419C1832370OMIM06292770125660
HP:0001644HP:0001644Dilated cardiomyopathy0ERBB3 CL E G H2065607598Lethal congenital contracture syndrome 2607598C1843478OMIM0953431190151
HP:0001644HP:0001644Dilated cardiomyopathy0ERBB3 CL E G H2065607598Lethal congenital contracture syndrome 2607598C1843478OMIM0943431190151
HP:0001644HP:0001644Dilated cardiomyopathy0FHL1 CL E G H2273300718Myopathy, reducing body, X-linked, childhood-onset300718C2678015OMIM04863702300163
HP:0001644HP:0001644Dilated cardiomyopathy0FHL1 CL E G H2273300718Myopathy, reducing body, X-linked, childhood-onset300718C2678015OMIM04373702300163
HP:0001644HP:0001644Dilated cardiomyopathy0FKRP CL E G H7914734515ORPHA067117997606596
HP:0001644HP:0001644Dilated cardiomyopathy0FKRP CL E G H7914734515ORPHA057217997606596
HP:0001644HP:0001644Dilated cardiomyopathy0FKTN CL E G H2218272VACTERL hydrocephalyORPHA05993622607440
HP:0001644HP:0001644Dilated cardiomyopathy0FKTN CL E G H2218272VACTERL hydrocephalyORPHA06793622607440
HP:0001644HP:0001644Dilated cardiomyopathy0GABRD CL E G H25631606ORPHA03614084137163
HP:0001644HP:0001644Dilated cardiomyopathy0GABRD CL E G H25631606ORPHA03404084137163
HP:0001644HP:0001644Dilated cardiomyopathy0GATA5 CL E G H140628617912CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 5617912CN873437OMIM019615802611496
HP:0001644HP:0001644Dilated cardiomyopathy0GATA5 CL E G H140628617912CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 5617912CN873437OMIM011615802611496
HP:0001644HP:0001644Dilated cardiomyopathy0HACD1 CL E G H92002020ORPHA0859639610467
HP:0001644HP:0001644Dilated cardiomyopathy0HACD1 CL E G H92002020ORPHA0479639610467
HP:0001644HP:0001644Dilated cardiomyopathy0HADH CL E G H303371212ORPHA01564799601609
HP:0001644HP:0001644Dilated cardiomyopathy0HADH CL E G H303371212ORPHA01374799601609
HP:0001644HP:0001644Dilated cardiomyopathy0ITGA7 CL E G H36792020ORPHA06286143600536
HP:0001644HP:0001644Dilated cardiomyopathy0ITGA7 CL E G H36792020ORPHA05236143600536
HP:0001644HP:0001644Dilated cardiomyopathy0KCNAB2 CL E G H85141606ORPHA0916229601142
HP:0001644HP:0001644Dilated cardiomyopathy0KCNAB2 CL E G H85141606ORPHA0886229601142
HP:0001644HP:0001644Dilated cardiomyopathy0LAMA3 CL E G H390979404ORPHA08556483600805
HP:0001644HP:0001644Dilated cardiomyopathy0LAMA3 CL E G H390979404ORPHA08156483600805
HP:0001644HP:0001644Dilated cardiomyopathy0LAMB3 CL E G H391479404ORPHA06646490150310
HP:0001644HP:0001644Dilated cardiomyopathy0LAMB3 CL E G H391479404ORPHA06226490150310
HP:0001644HP:0001644Dilated cardiomyopathy0LAMC2 CL E G H391879404ORPHA05796493150292
HP:0001644HP:0001644Dilated cardiomyopathy0LAMC2 CL E G H391879404ORPHA05486493150292
HP:0001644HP:0001644Dilated cardiomyopathy0LMNA CL E G H400098853ORPHA014866636150330
HP:0001644HP:0001644Dilated cardiomyopathy0LMNA CL E G H400098853ORPHA013476636150330
HP:0001644HP:0001644Dilated cardiomyopathy0LMNA CL E G H4000264ORPHA014866636150330
HP:0001644HP:0001644Dilated cardiomyopathy0LMNA CL E G H4000264ORPHA013476636150330
HP:0001644HP:0001644Dilated cardiomyopathy0MAP3K20 CL E G H517762020ORPHA016217797609479
HP:0001644HP:0001644Dilated cardiomyopathy0MAP3K20 CL E G H517762020ORPHA07617797609479
HP:0001644HP:0001644Dilated cardiomyopathy0MGME1 CL E G H92667615084Mitochondrial DNA depletion syndrome 11615084C3554462OMIM06916205615076
HP:0001644HP:0001644Dilated cardiomyopathy0MGME1 CL E G H92667615084Mitochondrial DNA depletion syndrome 11615084C3554462OMIM07516205615076
HP:0001644HP:0001644Dilated cardiomyopathy0MMP1 CL E G H431279408ORPHA0657155120353
HP:0001644HP:0001644Dilated cardiomyopathy0MMP1 CL E G H431279408ORPHA0637155120353
HP:0001644HP:0001644Dilated cardiomyopathy0MYH7 CL E G H462559135ORPHA032927577160760
HP:0001644HP:0001644Dilated cardiomyopathy0MYH7 CL E G H462559135ORPHA029607577160760
HP:0001644HP:0001644Dilated cardiomyopathy0MYH7 CL E G H4625160500Myopathy, distal, 1160500CN074249OMIM032927577160760
HP:0001644HP:0001644Dilated cardiomyopathy0MYH7 CL E G H4625160500Myopathy, distal, 1160500CN074249OMIM029607577160760
HP:0001644HP:0001644Dilated cardiomyopathy0MYL2 CL E G H46332020ORPHA04067583160781
HP:0001644HP:0001644Dilated cardiomyopathy0MYL2 CL E G H46332020ORPHA03557583160781
HP:0001644HP:0001644Dilated cardiomyopathy0MYPN CL E G H84665615248Dilated cardiomyopathy 1KK615248C3714995OMIM0103323246608517
HP:0001644HP:0001644Dilated cardiomyopathy0MYPN CL E G H84665615248Dilated cardiomyopathy 1KK615248C3714995OMIM088723246608517
HP:0001644HP:0001644Dilated cardiomyopathy0NUP107 CL E G H57122616730Nephrotic syndrome, type 11616730C4225228OMIM013429914607617
HP:0001644HP:0001644Dilated cardiomyopathy0NUP107 CL E G H57122616730Nephrotic syndrome, type 11616730C4225228OMIM012829914607617
HP:0001644HP:0001644Dilated cardiomyopathy0POLG CL E G H5428254892ORPHA017129179174763
HP:0001644HP:0001644Dilated cardiomyopathy0POLG CL E G H5428254892ORPHA014709179174763
HP:0001644HP:0001644Dilated cardiomyopathy0POLG CL E G H542870595ORPHA017129179174763
HP:0001644HP:0001644Dilated cardiomyopathy0POLG CL E G H542870595ORPHA014709179174763
HP:0001644HP:0001644Dilated cardiomyopathy0POLG2 CL E G H11232254892ORPHA02049180604983
HP:0001644HP:0001644Dilated cardiomyopathy0POLG2 CL E G H11232254892ORPHA01339180604983
HP:0001644HP:0001644Dilated cardiomyopathy0PRDM16 CL E G H639761606ORPHA098614000605557
HP:0001644HP:0001644Dilated cardiomyopathy0PRDM16 CL E G H639761606ORPHA088614000605557
HP:0001644HP:0001644Dilated cardiomyopathy0RERE CL E G H4731606ORPHA02579965605226
HP:0001644HP:0001644Dilated cardiomyopathy0RERE CL E G H4731606ORPHA02299965605226
HP:0001644HP:0001644Dilated cardiomyopathy0RRM2B CL E G H50484254892ORPHA027217296604712
HP:0001644HP:0001644Dilated cardiomyopathy0RRM2B CL E G H50484254892ORPHA026117296604712
HP:0001644HP:0001644Dilated cardiomyopathy0SELENON CL E G H571902020ORPHA050515999606210
HP:0001644HP:0001644Dilated cardiomyopathy0SELENON CL E G H571902020ORPHA045415999606210
HP:0001644HP:0001644Dilated cardiomyopathy0SGCB CL E G H6443604286Limb-girdle muscular dystrophy, type 2E604286C1858593OMIM032710806600900
HP:0001644HP:0001644Dilated cardiomyopathy0SGCB CL E G H6443604286Limb-girdle muscular dystrophy, type 2E604286C1858593OMIM037410806600900
HP:0001644HP:0001644Dilated cardiomyopathy0SKI CL E G H64971606ORPHA068610896164780
HP:0001644HP:0001644Dilated cardiomyopathy0SKI CL E G H64971606ORPHA062910896164780
HP:0001644HP:0001644Dilated cardiomyopathy0SLC25A4 CL E G H291254892ORPHA026110990103220
HP:0001644HP:0001644Dilated cardiomyopathy0SLC25A4 CL E G H291254892ORPHA025410990103220
HP:0001644HP:0001644Dilated cardiomyopathy0SLC2A10 CL E G H810313342ORPHA042413444606145
HP:0001644HP:0001644Dilated cardiomyopathy0SLC2A10 CL E G H810313342ORPHA039213444606145
HP:0001644HP:0001644Dilated cardiomyopathy0SYNE1 CL E G H2334598853ORPHA0417017089608441
HP:0001644HP:0001644Dilated cardiomyopathy0SYNE1 CL E G H2334598853ORPHA0364117089608441
HP:0001644HP:0001644Dilated cardiomyopathy0SYNE2 CL E G H2322498853ORPHA0222217084608442
HP:0001644HP:0001644Dilated cardiomyopathy0SYNE2 CL E G H2322498853ORPHA0187517084608442
HP:0001644HP:0001644Dilated cardiomyopathy0TMEM43 CL E G H7918898853ORPHA065328472612048
HP:0001644HP:0001644Dilated cardiomyopathy0TMEM43 CL E G H7918898853ORPHA058528472612048
HP:0001644HP:0001644Dilated cardiomyopathy0TPM2 CL E G H71692020ORPHA024212011190990
HP:0001644HP:0001644Dilated cardiomyopathy0TPM2 CL E G H71692020ORPHA023412011190990
HP:0001644HP:0001644Dilated cardiomyopathy0TPM3 CL E G H71702020ORPHA028312012191030
HP:0001644HP:0001644Dilated cardiomyopathy0TPM3 CL E G H71702020ORPHA026112012191030
HP:0001644HP:0001644Dilated cardiomyopathy0TSFM CL E G H10102610505Combined oxidative phosphorylation deficiency 3610505C1864840OMIM024412367604723
HP:0001644HP:0001644Dilated cardiomyopathy0TSFM CL E G H10102610505Combined oxidative phosphorylation deficiency 3610505C1864840OMIM018312367604723
HP:0001644HP:0001644Dilated cardiomyopathy0TWNK CL E G H5665270595ORPHA02701160606075
HP:0001644HP:0001644Dilated cardiomyopathy0TWNK CL E G H56652254892ORPHA02701160606075
HP:0001644HP:0001644Dilated cardiomyopathy0TWNK CL E G H5665270595ORPHA02341160606075
HP:0001644HP:0001644Dilated cardiomyopathy0TWNK CL E G H56652254892ORPHA02341160606075
HP:0001644HP:0001644Dilated cardiomyopathy0UBR1 CL E G H197131243800Johanson-Blizzard syndrome243800C0175692OMIM018716808605981
HP:0001644HP:0001644Dilated cardiomyopathy0UBR1 CL E G H197131243800Johanson-Blizzard syndrome243800C0175692OMIM014816808605981
HP:0001644HP:0001644Dilated cardiomyopathy0XRCC4 CL E G H7518616541Short stature, microcephaly, and endocrine dysfunction616541C4225288OMIM05412831194363
HP:0001644HP:0001644Dilated cardiomyopathy0XRCC4 CL E G H7518616541Short stature, microcephaly, and endocrine dysfunction616541C4225288OMIM06812831194363


Genes (117) :ABCC9 ACAD8 ACAD9 ACTA1 ACTC1 ACTN2 ADCY5 ALMS1 ANKRD1 ANKRD11 BAG3 BBS2 BOLA3 CHKB COL7A1 COX7B CPT2 CRYAB CSRP3 DES DMD DNAJC19 DOLK DPM3 DSG2 DSP EPG5 ERBB3 EYA4 FHL1 FHL2 FKRP FKTN GABRD GATA5 GATAD1 GLB1 HACD1 HADH HADHA HADHB HAMP HCCS HJV ITGA7 JUP KAT6B KCNAB2 LAMA3 LAMA4 LAMB3 LAMC2 LAMP2 LDB3 LIMS2 LMNA MAP3K20 MGME1 MMP1 MT-TK MYBPC3 MYH6 MYH7 MYL2 MYPN NDUFB11 NEBL NEXN NUP107 PGM1 PLN POLG POLG2 PPCS PRDM16 PSEN1 PSEN2 RAF1 RBCK1 RBM20 RERE RRM2B RYR1 SCN5A SDHA SDHAF1 SDHD SELENON SGCB SGCD SKI SLC25A4 SLC2A10 SPEG SYNE1 SYNE2 TAF1A TAZ TCAP TMEM43 TMPO TNNC1 TNNI3 TNNI3K TNNT2 TPM1 TPM2 TPM3 TRNK TSFM TTN TWNK TXNRD2 UBR1 VCL XK XRCC4

Diseases (124) :608569 154 611283 99901 611126 2020 255310 161800 613424 612158 324588 606703 64 203800 261250 613881 615981 614299 602541 79409 79408 2556 600649 608836 615184 607482 604765 601419 302045 310200 66634 610198 610768 263494 612937 612877 65282 615821 605676 242840 607598 217622 605362 300718 34515 607155 611615 253800 272 1606 617912 614672 230500 71212 231530 609015 79230 602390 601214 603736 79404 615235 34587 300257 601493 616827 264 168796 98855 98853 2229 181350 115200 212112 610140 352447 615084 615396 613252 59135 613426 160500 255160 615248 300952 613122 616730 614921 609909 254892 70595 607459 618189 615373 613694 613697 615916 615895 613172 601154 613642 252011 604286 606685 3342 615959 302060 111 607487 611879 613286 611880 616117 601494 611878 1349 610505 604145 613765 611705 243800 611407 300842 616541
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is August 2021 release.