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
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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 syndromeORPHA1126660601439
HP:0001644HP:0001644Dilated cardiomyopathy0ACAD8 CL E G H27034611283Deficiency of isobutyryl-CoA dehydrogenase611283C1969809OMIM130487604773
HP:0001644HP:0001644Dilated cardiomyopathy0ACAD9 CL E G H2897699901ORPHA156021497611103
HP:0001644HP:0001644Dilated cardiomyopathy0ACAD9 CL E G H28976611126Acyl-CoA dehydrogenase family, member 9, deficiency of611126C1970173OMIM156021497611103
HP:0001644HP:0001644Dilated cardiomyopathy0ACTA1 CL E G H58255310Congenital myopathy with fiber type disproportion255310C0546264OMIM1392129102610
HP:0001644HP:0001644Dilated cardiomyopathy0ACTC1 CL E G H70613424Dilated cardiomyopathy 1R613424C3150681OMIM1607143102540
HP:0001644HP:0001644Dilated cardiomyopathy0ACTC1 CL E G H70154Sandhaus Ben-Ami syndromeORPHA1607143102540
HP:0001644HP:0001644Dilated cardiomyopathy0ACTN2 CL E G H88612158Dilated cardiomyopathy 1AA612158C2677338OMIM11157164102573
HP:0001644HP:0001644Dilated cardiomyopathy0ACTN2 CL E G H88154Sandhaus Ben-Ami syndromeORPHA11157164102573
HP:0001644HP:0001644Dilated cardiomyopathy0ALMS1 CL E G H784064ORPHA14321428606844
HP:0001644HP:0001644Dilated cardiomyopathy0ALMS1 CL E G H7840203800Alstrom syndrome203800C0268425OMIM14321428606844
HP:0001644HP:0001644Dilated cardiomyopathy0ANKRD1 CL E G H27063154Sandhaus Ben-Ami syndromeORPHA138915819609599
HP:0001644HP:0001644Dilated cardiomyopathy0BAG3 CL E G H9531613881Dilated cardiomyopathy 1HH613881C3151293OMIM1856939603883
HP:0001644HP:0001644Dilated cardiomyopathy0BAG3 CL E G H9531154Sandhaus Ben-Ami syndromeORPHA1856939603883
HP:0001644HP:0001644Dilated cardiomyopathy0BOLA3 CL E G H388962614299Multiple mitochondrial dysfunctions syndrome 2614299C3280378OMIM17624415613183
HP:0001644HP:0001644Dilated cardiomyopathy0COX7B CL E G H13492556ORPHA11732291300885
HP:0001644HP:0001644Dilated cardiomyopathy0CPT2 CL E G H1376600649Carnitine palmitoyltransferase II deficiency, infantile600649C1833511OMIM17202330600650
HP:0001644HP:0001644Dilated cardiomyopathy0CPT2 CL E G H1376608836Carnitine palmitoyltransferase II deficiency, lethal neonatal608836C1833518OMIM17202330600650
HP:0001644HP:0001644Dilated cardiomyopathy0CRYAB CL E G H1410615184Dilated cardiomyopathy 1II615184C3554649OMIM12302389123590
HP:0001644HP:0001644Dilated cardiomyopathy0CRYAB CL E G H1410154Sandhaus Ben-Ami syndromeORPHA12302389123590
HP:0001644HP:0001644Dilated cardiomyopathy0CSRP3 CL E G H8048607482Dilated cardiomyopathy 1M607482C1843808OMIM13642472600824
HP:0001644HP:0001644Dilated cardiomyopathy0CSRP3 CL E G H8048154Sandhaus Ben-Ami syndromeORPHA13642472600824
HP:0001644HP:0001644Dilated cardiomyopathy0DES CL E G H1674604765Dilated cardiomyopathy 1I604765C1858154OMIM18182770125660
HP:0001644HP:0001644Dilated cardiomyopathy0DES CL E G H1674154Sandhaus Ben-Ami syndromeORPHA18182770125660
HP:0001644HP:0001644Dilated cardiomyopathy0DMD CL E G H1756302045Dilated cardiomyopathy 3B302045C3668940OMIM173702928300377
HP:0001644HP:0001644Dilated cardiomyopathy0DMD CL E G H1756310200Duchenne muscular dystrophy310200C0013264OMIM173702928300377
HP:0001644HP:0001644Dilated cardiomyopathy0DMD CL E G H1756154Sandhaus Ben-Ami syndromeORPHA173702928300377
HP:0001644HP:0001644Dilated cardiomyopathy0DNAJC19 CL E G H13111866634ORPHA111130528608977
HP:0001644HP:0001644Dilated cardiomyopathy0DNAJC19 CL E G H1311186101983-methylglutaconic aciduria type V610198C1857776OMIM111130528608977
HP:0001644HP:0001644Dilated cardiomyopathy0DOLK CL E G H22845610768Congenital disorder of glycosylation type 1M610768C1835849OMIM142423406610746
HP:0001644HP:0001644Dilated cardiomyopathy0DOLK CL E G H22845154Sandhaus Ben-Ami syndromeORPHA142423406610746
HP:0001644HP:0001644Dilated cardiomyopathy0DPM3 CL E G H54344263494ORPHA1603007605951
HP:0001644HP:0001644Dilated cardiomyopathy0DPM3 CL E G H54344612937Congenital disorder of glycosylation type 1O612937C2752007OMIM1603007605951
HP:0001644HP:0001644Dilated cardiomyopathy0DSG2 CL E G H1829612877Dilated cardiomyopathy 1BB612877C2752072OMIM113793049125671
HP:0001644HP:0001644Dilated cardiomyopathy0DSG2 CL E G H1829154Sandhaus Ben-Ami syndromeORPHA113793049125671
HP:0001644HP:0001644Dilated cardiomyopathy0DSP CL E G H183265282ORPHA133843052125647
HP:0001644HP:0001644Dilated cardiomyopathy0DSP CL E G H1832615821Cardiomyopathy, dilated, with woolly hair, keratoderma, and tooth agenesis615821C4014393OMIM133843052125647
HP:0001644HP:0001644Dilated cardiomyopathy0DSP CL E G H1832605676Dilated cardiomyopathy with woolly hair and keratoderma605676C1854063OMIM133843052125647
HP:0001644HP:0001644Dilated cardiomyopathy0EPG5 CL E G H57724242840Vici syndrome242840C1855772OMIM1121329331615068
HP:0001644HP:0001644Dilated cardiomyopathy0EYA4 CL E G H2070217622ORPHA16823522603550
HP:0001644HP:0001644Dilated cardiomyopathy0EYA4 CL E G H2070605362Dilated cardiomyopathy 1J605362C1854368OMIM16823522603550
HP:0001644HP:0001644Dilated cardiomyopathy0FHL2 CL E G H2274154Sandhaus Ben-Ami syndromeORPHA11693703602633
HP:0001644HP:0001644Dilated cardiomyopathy0FKRP CL E G H79147607155Limb-girdle muscular dystrophy-dystroglycanopathy, type C5607155C1846672OMIM178717997606596
HP:0001644HP:0001644Dilated cardiomyopathy0FKTN CL E G H2218611615Dilated cardiomyopathy 1X611615C1969024OMIM17833622607440
HP:0001644HP:0001644Dilated cardiomyopathy0FKTN CL E G H2218253800Fukuyama congenital muscular dystrophy253800C0410174OMIM17833622607440
HP:0001644HP:0001644Dilated cardiomyopathy0FKTN CL E G H2218154Sandhaus Ben-Ami syndromeORPHA17833622607440
HP:0001644HP:0001644Dilated cardiomyopathy0GATAD1 CL E G H57798614672Cardiomyopathy, dilated, 2b614672C3553409OMIM149829941614518
HP:0001644HP:0001644Dilated cardiomyopathy0GATAD1 CL E G H57798154Sandhaus Ben-Ami syndromeORPHA149829941614518
HP:0001644HP:0001644Dilated cardiomyopathy0GLB1 CL E G H2720230500Infantile GM1 gangliosidosis230500C0268271OMIM16964298611458
HP:0001644HP:0001644Dilated cardiomyopathy0HADH CL E G H3033231530Deficiency of 3-hydroxyacyl-CoA dehydrogenase231530C1291230OMIM11684799601609
HP:0001644HP:0001644Dilated cardiomyopathy0HADHA CL E G H3030609015Mitochondrial trifunctional protein deficiency609015C0342786OMIM16304801600890
HP:0001644HP:0001644Dilated cardiomyopathy0HADHB CL E G H3032609015Mitochondrial trifunctional protein deficiency609015C0342786OMIM12634803143450
HP:0001644HP:0001644Dilated cardiomyopathy0HAMP CL E G H5781779230ORPHA16315598606464
HP:0001644HP:0001644Dilated cardiomyopathy0HCCS CL E G H30522556ORPHA12184837300056
HP:0001644HP:0001644Dilated cardiomyopathy0HJV CL E G H14873879230ORPHA14184887608374
HP:0001644HP:0001644Dilated cardiomyopathy0HJV CL E G H148738602390Hemochromatosis type 2A602390C1865614OMIM14184887608374
HP:0001644HP:0001644Dilated cardiomyopathy0JUP CL E G H3728601214Naxos disease601214C1832600OMIM18926207173325
HP:0001644HP:0001644Dilated cardiomyopathy0KAT6B CL E G H23522603736Young Simpson syndrome603736C1863557OMIM160517582605880
HP:0001644HP:0001644Dilated cardiomyopathy0LAMA4 CL E G H3910615235Dilated cardiomyopathy 1JJ615235C3808935OMIM113546484600133
HP:0001644HP:0001644Dilated cardiomyopathy0LAMA4 CL E G H3910154Sandhaus Ben-Ami syndromeORPHA113546484600133
HP:0001644HP:0001644Dilated cardiomyopathy0LAMP2 CL E G H392034587ORPHA17596501309060
HP:0001644HP:0001644Dilated cardiomyopathy0LAMP2 CL E G H3920300257Danon disease300257C0878677OMIM17596501309060
HP:0001644HP:0001644Dilated cardiomyopathy0LDB3 CL E G H11155601493Dilated cardiomyopathy 1C601493C1832244OMIM1106015710605906
HP:0001644HP:0001644Dilated cardiomyopathy0LDB3 CL E G H11155154Sandhaus Ben-Ami syndromeORPHA1106015710605906
HP:0001644HP:0001644Dilated cardiomyopathy0LIMS2 CL E G H55679616827Muscular dystrophy, limb-girdle, type 2W616827C4225192OMIM121916084607908
HP:0001644HP:0001644Dilated cardiomyopathy0LMNA CL E G H4000168796ORPHA116226636150330
HP:0001644HP:0001644Dilated cardiomyopathy0LMNA CL E G H400098855ORPHA116226636150330
HP:0001644HP:0001644Dilated cardiomyopathy0LMNA CL E G H40002229ORPHA116226636150330
HP:0001644HP:0001644Dilated cardiomyopathy0LMNA CL E G H4000181350Benign scapuloperoneal muscular dystrophy with cardiomyopathy181350C0410190OMIM116226636150330
HP:0001644HP:0001644Dilated cardiomyopathy0LMNA CL E G H4000115200Dilated cardiomyopathy 1A115200C1449563OMIM116226636150330
HP:0001644HP:0001644Dilated cardiomyopathy0LMNA CL E G H4000212112Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome212112C0796031OMIM116226636150330
HP:0001644HP:0001644Dilated cardiomyopathy0LMNA CL E G H4000610140Heart-hand syndrome, Slovenian type610140C1857829OMIM116226636150330
HP:0001644HP:0001644Dilated cardiomyopathy0MGME1 CL E G H92667352447ORPHA17816205615076
HP:0001644HP:0001644Dilated cardiomyopathy0MT-TK CL E G H45661349Chromosome 9, partial monosomy 9pC2931695ORPHA17489590060
HP:0001644HP:0001644Dilated cardiomyopathy0MYBPC3 CL E G H4607615396Left ventricular noncompaction 10615396C3715165OMIM129817551600958
HP:0001644HP:0001644Dilated cardiomyopathy0MYBPC3 CL E G H4607154Sandhaus Ben-Ami syndromeORPHA129817551600958
HP:0001644HP:0001644Dilated cardiomyopathy0MYH6 CL E G H4624613252Dilated cardiomyopathy 1EE613252C2750466OMIM117767576160710
HP:0001644HP:0001644Dilated cardiomyopathy0MYH6 CL E G H4624154Sandhaus Ben-Ami syndromeORPHA117767576160710
HP:0001644HP:0001644Dilated cardiomyopathy0MYH7 CL E G H4625255310Congenital myopathy with fiber type disproportion255310C0546264OMIM136127577160760
HP:0001644HP:0001644Dilated cardiomyopathy0MYH7 CL E G H4625613426Dilated cardiomyopathy 1S613426C1834481OMIM136127577160760
HP:0001644HP:0001644Dilated cardiomyopathy0MYH7 CL E G H4625255160Myopathy, myosin storage, autosomal recessive255160C1850709OMIM136127577160760
HP:0001644HP:0001644Dilated cardiomyopathy0MYH7 CL E G H4625154Sandhaus Ben-Ami syndromeORPHA136127577160760
HP:0001644HP:0001644Dilated cardiomyopathy0MYPN CL E G H84665154Sandhaus Ben-Ami syndromeORPHA1126323246608517
HP:0001644HP:0001644Dilated cardiomyopathy0NDUFB11 CL E G H545392556ORPHA118020372300403
HP:0001644HP:0001644Dilated cardiomyopathy0NDUFB11 CL E G H54539300952Linear skin defects with multiple congenital anomalies 3300952C4225421OMIM118020372300403
HP:0001644HP:0001644Dilated cardiomyopathy0NEBL CL E G H10529154Sandhaus Ben-Ami syndromeORPHA182116932605491
HP:0001644HP:0001644Dilated cardiomyopathy0NEXN CL E G H91624613122Dilated cardiomyopathy 1CC613122C2751084OMIM156429557613121
HP:0001644HP:0001644Dilated cardiomyopathy0NEXN CL E G H91624154Sandhaus Ben-Ami syndromeORPHA156429557613121
HP:0001644HP:0001644Dilated cardiomyopathy0PGM1 CL E G H5236614921Congenital disorder of glycosylation type 1t614921C2752015OMIM12758905171900
HP:0001644HP:0001644Dilated cardiomyopathy0PLN CL E G H5350609909Dilated cardiomyopathy 1P609909C1835928OMIM11629080172405
HP:0001644HP:0001644Dilated cardiomyopathy0PLN CL E G H5350154Sandhaus Ben-Ami syndromeORPHA11629080172405
HP:0001644HP:0001644Dilated cardiomyopathy0POLG CL E G H5428607459Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis607459C1843851OMIM119179179174763
HP:0001644HP:0001644Dilated cardiomyopathy0PPCS CL E G H79717618189CARDIOMYOPATHY, DILATED, 2C618189OMIM112525686609853
HP:0001644HP:0001644Dilated cardiomyopathy0PPCS CL E G H79717154Sandhaus Ben-Ami syndromeORPHA112525686609853
HP:0001644HP:0001644Dilated cardiomyopathy0PRDM16 CL E G H63976615373Left ventricular noncompaction 8615373C3809288OMIM1108114000605557
HP:0001644HP:0001644Dilated cardiomyopathy0PRDM16 CL E G H63976154Sandhaus Ben-Ami syndromeORPHA1108114000605557
HP:0001644HP:0001644Dilated cardiomyopathy0PSEN1 CL E G H5663613694Cardiomyopathy, dilated, 1u613694C3160720OMIM14529508104311
HP:0001644HP:0001644Dilated cardiomyopathy0PSEN1 CL E G H5663154Sandhaus Ben-Ami syndromeORPHA14529508104311
HP:0001644HP:0001644Dilated cardiomyopathy0PSEN2 CL E G H5664613697Dilated cardiomyopathy 1V613697C3150958OMIM12379509600759
HP:0001644HP:0001644Dilated cardiomyopathy0PSEN2 CL E G H5664154Sandhaus Ben-Ami syndromeORPHA12379509600759
HP:0001644HP:0001644Dilated cardiomyopathy0RAF1 CL E G H5894615916Cardiomyopathy, dilated, 1NN615916C4014656OMIM18279829164760
HP:0001644HP:0001644Dilated cardiomyopathy0RAF1 CL E G H5894154Sandhaus Ben-Ami syndromeORPHA18279829164760
HP:0001644HP:0001644Dilated cardiomyopathy0RBCK1 CL E G H10616615895Polyglucosan body myopathy 1 with or without immunodeficiency615895C4014605OMIM136415864610924
HP:0001644HP:0001644Dilated cardiomyopathy0RBM20 CL E G H282996613172Dilated cardiomyopathy 1DD613172C2750995OMIM1135427424613171
HP:0001644HP:0001644Dilated cardiomyopathy0RBM20 CL E G H282996154Sandhaus Ben-Ami syndromeORPHA1135427424613171
HP:0001644HP:0001644Dilated cardiomyopathy0RYR1 CL E G H6261255310Congenital myopathy with fiber type disproportion255310C0546264OMIM1506210483180901
HP:0001644HP:0001644Dilated cardiomyopathy0SCN5A CL E G H6331601154Dilated cardiomyopathy 1E601154C1832680OMIM1317110593600163
HP:0001644HP:0001644Dilated cardiomyopathy0SCN5A CL E G H6331154Sandhaus Ben-Ami syndromeORPHA1317110593600163
HP:0001644HP:0001644Dilated cardiomyopathy0SDHA CL E G H6389613642Dilated cardiomyopathy 1GG613642C3150898OMIM1218610680600857
HP:0001644HP:0001644Dilated cardiomyopathy0SDHA CL E G H6389252011Mitochondrial complex II deficiency252011C1855008OMIM1218610680600857
HP:0001644HP:0001644Dilated cardiomyopathy0SDHA CL E G H6389154Sandhaus Ben-Ami syndromeORPHA1218610680600857
HP:0001644HP:0001644Dilated cardiomyopathy0SDHAF1 CL E G H644096252011Mitochondrial complex II deficiency252011C1855008OMIM16033867612848
HP:0001644HP:0001644Dilated cardiomyopathy0SDHD CL E G H6392252011Mitochondrial complex II deficiency252011C1855008OMIM160710683602690
HP:0001644HP:0001644Dilated cardiomyopathy0SELENON CL E G H57190255310Congenital myopathy with fiber type disproportion255310C0546264OMIM153715999606210
HP:0001644HP:0001644Dilated cardiomyopathy0SGCD CL E G H6444606685Dilated cardiomyopathy 1L606685C1847667OMIM158710807601411
HP:0001644HP:0001644Dilated cardiomyopathy0SGCD CL E G H6444154Sandhaus Ben-Ami syndromeORPHA158710807601411
HP:0001644HP:0001644Dilated cardiomyopathy0SPEG CL E G H10290615959Myopathy, centronuclear, 5615959C4014814OMIM190716901615950
HP:0001644HP:0001644Dilated cardiomyopathy0TAF1A CL E G H9015154Sandhaus Ben-Ami syndromeORPHA13511532604903
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 1N607487C1843791OMIM125411610604488
HP:0001644HP:0001644Dilated cardiomyopathy0TCAP CL E G H8557154Sandhaus Ben-Ami syndromeORPHA125411610604488
HP:0001644HP:0001644Dilated cardiomyopathy0TMPO CL E G H7112154Sandhaus Ben-Ami syndromeORPHA149311875188380
HP:0001644HP:0001644Dilated cardiomyopathy0TNNC1 CL E G H7134611879Dilated cardiomyopathy 1Z611879C2678475OMIM125111943191040
HP:0001644HP:0001644Dilated cardiomyopathy0TNNC1 CL E G H7134154Sandhaus Ben-Ami syndromeORPHA125111943191040
HP:0001644HP:0001644Dilated cardiomyopathy0TNNI3 CL E G H7137613286Dilated cardiomyopathy 1FF613286C2750091OMIM159411947191044
HP:0001644HP:0001644Dilated cardiomyopathy0TNNI3 CL E G H7137611880Dilated cardiomyopathy 2A611880C2678474OMIM159411947191044
HP:0001644HP:0001644Dilated cardiomyopathy0TNNI3 CL E G H7137154Sandhaus Ben-Ami syndromeORPHA159411947191044
HP:0001644HP:0001644Dilated cardiomyopathy0TNNI3K CL E G H51086616117Cardiac conduction disease with or without dilated cardiomyopathy616117C4015285OMIM151519661613932
HP:0001644HP:0001644Dilated cardiomyopathy0TNNT2 CL E G H7139601494Left ventricular noncompaction 6601494C1832243OMIM173411949191045
HP:0001644HP:0001644Dilated cardiomyopathy0TNNT2 CL E G H7139154Sandhaus Ben-Ami syndromeORPHA173411949191045
HP:0001644HP:0001644Dilated cardiomyopathy0TPM1 CL E G H7168611878Dilated cardiomyopathy 1Y611878C2678476OMIM169412010191010
HP:0001644HP:0001644Dilated cardiomyopathy0TPM1 CL E G H7168154Sandhaus Ben-Ami syndromeORPHA169412010191010
HP:0001644HP:0001644Dilated cardiomyopathy0TPM2 CL E G H7169255310Congenital myopathy with fiber type disproportion255310C0546264OMIM128012011190990
HP:0001644HP:0001644Dilated cardiomyopathy0TPM3 CL E G H7170255310Congenital myopathy with fiber type disproportion255310C0546264OMIM130012012191030
HP:0001644HP:0001644Dilated cardiomyopathy0TTN CL E G H7273604145Dilated cardiomyopathy 1G604145C1858763OMIM12285912403188840
HP:0001644HP:0001644Dilated cardiomyopathy0TTN CL E G H7273613765Familial hypertrophic cardiomyopathy 9613765C1861065OMIM12285912403188840
HP:0001644HP:0001644Dilated cardiomyopathy0TTN CL E G H7273611705Myopathy, early-onset, with fatal cardiomyopathy611705C2673677OMIM12285912403188840
HP:0001644HP:0001644Dilated cardiomyopathy0TTN CL E G H7273154Sandhaus Ben-Ami syndromeORPHA12285912403188840
HP:0001644HP:0001644Dilated cardiomyopathy0TWNK CL E G H56652607459Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis607459C1843851OMIM13081160606075
HP:0001644HP:0001644Dilated cardiomyopathy0TXNRD2 CL E G H10587154Sandhaus Ben-Ami syndromeORPHA195818155606448
HP:0001644HP:0001644Dilated cardiomyopathy0VCL CL E G H7414611407Dilated cardiomyopathy 1W611407C1969639OMIM197812665193065
HP:0001644HP:0001644Dilated cardiomyopathy0VCL CL E G H7414154Sandhaus Ben-Ami syndromeORPHA197812665193065
HP:0001644HP:0001644Dilated cardiomyopathy0XK CL E G H7504300842McLeod neuroacanthocytosis syndrome300842C0398568OMIM118812811314850
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0001644HP:0001644Dilated cardiomyopathy0ABCC9 CL E G H10060608569Dilated cardiomyopathy 1O608569C1837839OMIM0126660601439
HP:0001644HP:0001644Dilated cardiomyopathy0ACTA1 CL E G H582020ORPHA0392129102610
HP:0001644HP:0001644Dilated cardiomyopathy0ACTA1 CL E G H58161800Nemaline myopathy 3161800C3711389OMIM0392129102610
HP:0001644HP:0001644Dilated cardiomyopathy0ADCY5 CL E G H111324588ORPHA0480236600293
HP:0001644HP:0001644Dilated cardiomyopathy0ADCY5 CL E G H111606703Dyskinesia, familial, with facial myokymia606703C1847627OMIM0480236600293
HP:0001644HP:0001644Dilated cardiomyopathy0ANKRD11 CL E G H2912326125016q24.3 microdeletion syndromeCN202174ORPHA0151521316611192
HP:0001644HP:0001644Dilated cardiomyopathy0BBS2 CL E G H583615981Bardet-Biedl syndrome 2615981C2936863OMIM0712967606151
HP:0001644HP:0001644Dilated cardiomyopathy0CHKB CL E G H1120602541Muscular dystrophy, congenital, megaconial type602541C1865233OMIM04191938612395
HP:0001644HP:0001644Dilated cardiomyopathy0COL7A1 CL E G H129479408ORPHA026162214120120
HP:0001644HP:0001644Dilated cardiomyopathy0COL7A1 CL E G H129479409ORPHA026162214120120
HP:0001644HP:0001644Dilated cardiomyopathy0DES CL E G H1674601419Myofibrillar myopathy 1601419C1832370OMIM08182770125660
HP:0001644HP:0001644Dilated cardiomyopathy0ERBB3 CL E G H2065607598Lethal congenital contracture syndrome 2607598C1843478OMIM0973431190151
HP:0001644HP:0001644Dilated cardiomyopathy0FHL1 CL E G H2273300718Myopathy, reducing body, X-linked, childhood-onset300718C2678015OMIM05173702300163
HP:0001644HP:0001644Dilated cardiomyopathy0FKRP CL E G H7914734515ORPHA078717997606596
HP:0001644HP:0001644Dilated cardiomyopathy0FKTN CL E G H2218272VACTERL hydrocephalyORPHA07833622607440
HP:0001644HP:0001644Dilated cardiomyopathy0GABRD CL E G H25631606ORPHA03974084137163
HP:0001644HP:0001644Dilated cardiomyopathy0GATA5 CL E G H140628617912CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 5617912CN873437OMIM027015802611496
HP:0001644HP:0001644Dilated cardiomyopathy0HACD1 CL E G H92002020ORPHA01099639610467
HP:0001644HP:0001644Dilated cardiomyopathy0HADH CL E G H303371212ORPHA01684799601609
HP:0001644HP:0001644Dilated cardiomyopathy0ITGA7 CL E G H36792020ORPHA07186143600536
HP:0001644HP:0001644Dilated cardiomyopathy0KCNAB2 CL E G H85141606ORPHA0916229601142
HP:0001644HP:0001644Dilated cardiomyopathy0LAMA3 CL E G H390979404ORPHA010196483600805
HP:0001644HP:0001644Dilated cardiomyopathy0LAMB3 CL E G H391479404ORPHA08196490150310
HP:0001644HP:0001644Dilated cardiomyopathy0LAMC2 CL E G H391879404ORPHA07236493150292
HP:0001644HP:0001644Dilated cardiomyopathy0LMNA CL E G H400098853ORPHA016226636150330
HP:0001644HP:0001644Dilated cardiomyopathy0LMNA CL E G H4000264ORPHA016226636150330
HP:0001644HP:0001644Dilated cardiomyopathy0MAP3K20 CL E G H517762020ORPHA024317797609479
HP:0001644HP:0001644Dilated cardiomyopathy0MGME1 CL E G H92667615084Mitochondrial DNA depletion syndrome 11615084C3554462OMIM07816205615076
HP:0001644HP:0001644Dilated cardiomyopathy0MMP1 CL E G H431279408ORPHA0727155120353
HP:0001644HP:0001644Dilated cardiomyopathy0MYH7 CL E G H462559135ORPHA036127577160760
HP:0001644HP:0001644Dilated cardiomyopathy0MYH7 CL E G H4625160500Myopathy, distal, 1160500CN074249OMIM036127577160760
HP:0001644HP:0001644Dilated cardiomyopathy0MYL2 CL E G H46332020ORPHA04457583160781
HP:0001644HP:0001644Dilated cardiomyopathy0MYPN CL E G H84665615248Dilated cardiomyopathy 1KK615248C3714995OMIM0126323246608517
HP:0001644HP:0001644Dilated cardiomyopathy0NUP107 CL E G H57122616730Nephrotic syndrome, type 11616730C4225228OMIM014929914607617
HP:0001644HP:0001644Dilated cardiomyopathy0POLG CL E G H542870595ORPHA019179179174763
HP:0001644HP:0001644Dilated cardiomyopathy0POLG CL E G H5428254892ORPHA019179179174763
HP:0001644HP:0001644Dilated cardiomyopathy0POLG2 CL E G H11232254892ORPHA02409180604983
HP:0001644HP:0001644Dilated cardiomyopathy0PRDM16 CL E G H639761606ORPHA0108114000605557
HP:0001644HP:0001644Dilated cardiomyopathy0RERE CL E G H4731606ORPHA03439965605226
HP:0001644HP:0001644Dilated cardiomyopathy0RRM2B CL E G H50484254892ORPHA029317296604712
HP:0001644HP:0001644Dilated cardiomyopathy0SELENON CL E G H571902020ORPHA053715999606210
HP:0001644HP:0001644Dilated cardiomyopathy0SGCB CL E G H6443604286Limb-girdle muscular dystrophy, type 2E604286C1858593OMIM041910806600900
HP:0001644HP:0001644Dilated cardiomyopathy0SKI CL E G H64971606ORPHA091010896164780
HP:0001644HP:0001644Dilated cardiomyopathy0SLC25A4 CL E G H291254892ORPHA027810990103220
HP:0001644HP:0001644Dilated cardiomyopathy0SLC2A10 CL E G H810313342ORPHA049313444606145
HP:0001644HP:0001644Dilated cardiomyopathy0SYNE1 CL E G H2334598853ORPHA0459817089608441
HP:0001644HP:0001644Dilated cardiomyopathy0SYNE2 CL E G H2322498853ORPHA0249717084608442
HP:0001644HP:0001644Dilated cardiomyopathy0TMEM43 CL E G H7918898853ORPHA074028472612048
HP:0001644HP:0001644Dilated cardiomyopathy0TPM2 CL E G H71692020ORPHA028012011190990
HP:0001644HP:0001644Dilated cardiomyopathy0TPM3 CL E G H71702020ORPHA030012012191030
HP:0001644HP:0001644Dilated cardiomyopathy0TSFM CL E G H10102610505Combined oxidative phosphorylation deficiency 3610505C1864840OMIM030212367604723
HP:0001644HP:0001644Dilated cardiomyopathy0TWNK CL E G H5665270595ORPHA03081160606075
HP:0001644HP:0001644Dilated cardiomyopathy0TWNK CL E G H56652254892ORPHA03081160606075
HP:0001644HP:0001644Dilated cardiomyopathy0UBR1 CL E G H197131243800Johanson-Blizzard syndrome243800C0175692OMIM023616808605981
HP:0001644HP:0001644Dilated cardiomyopathy0XRCC4 CL E G H7518616541Short stature, microcephaly, and endocrine dysfunction616541C4225288OMIM08612831194363


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 98853 2229 264 168796 98855 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.