Human Phenotype Ontology 
Grandparent Node:
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Abnormality of prenatal development or birth (HP:0001197)help
Grandparent Node:
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Edema (HP:0000969)help
Parent Node:
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Hydrops fetalis (HP:0001789)help
..Starting node
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Nonimmune hydrops fetalis (HP:0001790)help
Term ID: 1790
Name: Nonimmune hydrops fetalis
Synonym: Hydrops fetalis, non-immune; Hydrops fetalis, nonimmune; Non-immune fetal hydrops; Non-immune foetal hydrops; Nonimmune hydrops
Definition: A type of hydrops fetalis in which there is no identifiable circulating antibody to red blood cell antigens .
Comments:
Reference: HP:0001790
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandobsolete Severe hydrops fetalis (HP:0005099) help
InputHPO IDHPO termDistanceGeneGene id entrezHGNC IDDiseaseIdDiseaseNameFrequencyOnsetHGMD variantsClinVar variants
 
HPO disease - gene - phenotype typical associations:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0001790HP:0001790Nonimmune hydrops fetalis0ADA2 CL E G H518161839ORPHA:124Blackfan-Diamond anemiaHP:0040284 - Very rare22
HP:0001790HP:0001790Nonimmune hydrops fetalis0ALG1 CL E G H5605218294OMIM:608540Congenital disorder of glycosylation, type Ik.58
HP:0001790HP:0001790Nonimmune hydrops fetalis0ALPK3 CL E G H5753817574OMIM:618052Cardiomyopathy, familial hypertrophic 2789
HP:0001790HP:0001790Nonimmune hydrops fetalis0CALCRL CL E G H1020316709OMIM:618773LYMPHATIC MALFORMATION 8; LMPHM83
HP:0001790HP:0001790Nonimmune hydrops fetalis0CARS2 CL E G H7958725695ORPHA:477774Combined oxidative phosphorylation defect type 27HP:0040283 - Occasional35
HP:0001790HP:0001790Nonimmune hydrops fetalis0COL1A1 CL E G H12772197OMIM:166210Osteogenesis imperfecta, type IIA.373
HP:0001790HP:0001790Nonimmune hydrops fetalis0COL1A2 CL E G H12782198OMIM:166210Osteogenesis imperfecta, type IIA.243
HP:0001790HP:0001790Nonimmune hydrops fetalis0CTSA CL E G H54769251OMIM:256540Galactosialidosis51
HP:0001790HP:0001790Nonimmune hydrops fetalis0EPHB4 CL E G H20503395ORPHA:137667Capillary malformation-arteriovenous malformationHP:0040284 - Very rare3
HP:0001790HP:0001790Nonimmune hydrops fetalis0EPHB4 CL E G H20503395OMIM:617300Lymphatic malformation 7.3
HP:0001790HP:0001790Nonimmune hydrops fetalis0FLT4 CL E G H23243767OMIM:153100Lymphatic malformation 190
HP:0001790HP:0001790Nonimmune hydrops fetalis0FOXC2 CL E G H23033801OMIM:153400Lymphedema-Distichiasis syndrome20
HP:0001790HP:0001790Nonimmune hydrops fetalis0FOXF1 CL E G H22943809OMIM:265380Alveolar capillary dysplasia with misalignment of pulmonary veins61
HP:0001790HP:0001790Nonimmune hydrops fetalis0GATA1 CL E G H26234170ORPHA:124Blackfan-Diamond anemiaHP:0040284 - Very rare29
HP:0001790HP:0001790Nonimmune hydrops fetalis0GATA1 CL E G H26234170ORPHA:79277Congenital erythropoietic porphyriaHP:0040282 - Frequent29
HP:0001790HP:0001790Nonimmune hydrops fetalis0GATB CL E G H51888849OMIM:618838COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 41; COXPD41
HP:0001790HP:0001790Nonimmune hydrops fetalis0GATC CL E G H28345925068OMIM:618839COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 42; COXPD421
HP:0001790HP:0001790Nonimmune hydrops fetalis0GBA1 CL E G H26294177OMIM:608013Gaucher disease, perinatal lethal
HP:0001790HP:0001790Nonimmune hydrops fetalis0LBR CL E G H39306518OMIM:215140Greenberg dysplasia70
HP:0001790HP:0001790Nonimmune hydrops fetalis0MCM10 CL E G H5538818043OMIM:619313IMMUNODEFICIENCY 80 WITH OR WITHOUT CONGENITAL CARDIOMYOPATHY; IMD80
HP:0001790HP:0001790Nonimmune hydrops fetalis0MDFIC CL E G H2996928870OMIM:620014
HP:0001790HP:0001790Nonimmune hydrops fetalis0NDUFB10 CL E G H47167696OMIM:619003MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 35; MC1DN35
HP:0001790HP:0001790Nonimmune hydrops fetalis0NR1H4 CL E G H99717967OMIM:617049CHOLESTASIS, PROGRESSIVE FAMILIAL INTRAHEPATIC, 5; PFIC514
HP:0001790HP:0001790Nonimmune hydrops fetalis0PIEZO1 CL E G H978028993OMIM:616843Lymphedema, hereditary, III.36
HP:0001790HP:0001790Nonimmune hydrops fetalis0PKLR CL E G H53139020OMIM:266200Pyruvate kinase deficiency of red cellsHP:0040283 - Occasional51
HP:0001790HP:0001790Nonimmune hydrops fetalis0PMM2 CL E G H53739115OMIM:212065Congenital disorder of glycosylation, type Ia.150
HP:0001790HP:0001790Nonimmune hydrops fetalis0QRSL1 CL E G H5527821020OMIM:618835COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 40; COXPD40
HP:0001790HP:0001790Nonimmune hydrops fetalis0RASA1 CL E G H59219871ORPHA:137667Capillary malformation-arteriovenous malformationHP:0040284 - Very rare88
HP:0001790HP:0001790Nonimmune hydrops fetalis0RPL11 CL E G H613510301ORPHA:124Blackfan-Diamond anemiaHP:0040284 - Very rare22
HP:0001790HP:0001790Nonimmune hydrops fetalis0RPL15 CL E G H613810306ORPHA:124Blackfan-Diamond anemiaHP:0040284 - Very rare3
HP:0001790HP:0001790Nonimmune hydrops fetalis0RPL18 CL E G H614110310ORPHA:124Blackfan-Diamond anemiaHP:0040284 - Very rare
HP:0001790HP:0001790Nonimmune hydrops fetalis0RPL26 CL E G H615410327ORPHA:124Blackfan-Diamond anemiaHP:0040284 - Very rare3
HP:0001790HP:0001790Nonimmune hydrops fetalis0RPL27 CL E G H615510328ORPHA:124Blackfan-Diamond anemiaHP:0040284 - Very rare1
HP:0001790HP:0001790Nonimmune hydrops fetalis0RPL31 CL E G H616010334ORPHA:124Blackfan-Diamond anemiaHP:0040284 - Very rare
HP:0001790HP:0001790Nonimmune hydrops fetalis0RPL35 CL E G H1122410344ORPHA:124Blackfan-Diamond anemiaHP:0040284 - Very rare
HP:0001790HP:0001790Nonimmune hydrops fetalis0RPL35A CL E G H616510345ORPHA:124Blackfan-Diamond anemiaHP:0040284 - Very rare11
HP:0001790HP:0001790Nonimmune hydrops fetalis0RPL5 CL E G H612510360ORPHA:124Blackfan-Diamond anemiaHP:0040284 - Very rare40
HP:0001790HP:0001790Nonimmune hydrops fetalis0RPS10 CL E G H620410383ORPHA:124Blackfan-Diamond anemiaHP:0040284 - Very rare26
HP:0001790HP:0001790Nonimmune hydrops fetalis0RPS15A CL E G H621010389ORPHA:124Blackfan-Diamond anemiaHP:0040284 - Very rare
HP:0001790HP:0001790Nonimmune hydrops fetalis0RPS17 CL E G H621810397ORPHA:124Blackfan-Diamond anemiaHP:0040284 - Very rare5
HP:0001790HP:0001790Nonimmune hydrops fetalis0RPS19 CL E G H622310402ORPHA:124Blackfan-Diamond anemiaHP:0040284 - Very rare42
HP:0001790HP:0001790Nonimmune hydrops fetalis0RPS20 CL E G H622410405ORPHA:124Blackfan-Diamond anemiaHP:0040284 - Very rare1
HP:0001790HP:0001790Nonimmune hydrops fetalis0RPS24 CL E G H622910411ORPHA:124Blackfan-Diamond anemiaHP:0040284 - Very rare22
HP:0001790HP:0001790Nonimmune hydrops fetalis0RPS26 CL E G H623110414ORPHA:124Blackfan-Diamond anemiaHP:0040284 - Very rare20
HP:0001790HP:0001790Nonimmune hydrops fetalis0RPS27 CL E G H623210416ORPHA:124Blackfan-Diamond anemiaHP:0040284 - Very rare1
HP:0001790HP:0001790Nonimmune hydrops fetalis0RPS28 CL E G H623410418ORPHA:124Blackfan-Diamond anemiaHP:0040284 - Very rare1
HP:0001790HP:0001790Nonimmune hydrops fetalis0RPS29 CL E G H623510419ORPHA:124Blackfan-Diamond anemiaHP:0040284 - Very rare3
HP:0001790HP:0001790Nonimmune hydrops fetalis0RPS7 CL E G H620110440ORPHA:124Blackfan-Diamond anemiaHP:0040284 - Very rare20
HP:0001790HP:0001790Nonimmune hydrops fetalis0SCN5A CL E G H633110593OMIM:603830Long QT syndrome 31134
HP:0001790HP:0001790Nonimmune hydrops fetalis0SLC35D1 CL E G H2316920800OMIM:269250Schneckenbecken dysplasia9
HP:0001790HP:0001790Nonimmune hydrops fetalis0SOX18 CL E G H5434511194OMIM:607823Hypotrichosis-Lymphedema-Telangiectasia syndrome.7
HP:0001790HP:0001790Nonimmune hydrops fetalis0SOX18 CL E G H5434511194OMIM:137940Hypotrichosis-Lymphedema-Telangiectasia-Renal defect syndrome7
HP:0001790HP:0001790Nonimmune hydrops fetalis0TSR2 CL E G H9012125455ORPHA:124Blackfan-Diamond anemiaHP:0040284 - Very rare1
HP:0001790HP:0001790Nonimmune hydrops fetalis0UROD CL E G H738912591ORPHA:95159Hepatoerythropoietic porphyriaHP:0040282 - Frequent31
HP:0001790HP:0001790Nonimmune hydrops fetalis0UROS CL E G H739012592ORPHA:79277Congenital erythropoietic porphyriaHP:0040282 - Frequent41


Genes (52) :ADA2 ALG1 ALPK3 CALCRL CARS2 COL1A1 COL1A2 CTSA EPHB4 FLT4 FOXC2 FOXF1 GATA1 GATB GATC GBA1 LBR MCM10 MDFIC NDUFB10 NR1H4 PIEZO1 PKLR PMM2 QRSL1 RASA1 RPL11 RPL15 RPL18 RPL26 RPL27 RPL31 RPL35 RPL35A RPL5 RPS10 RPS15A RPS17 RPS19 RPS20 RPS24 RPS26 RPS27 RPS28 RPS29 RPS7 SCN5A SLC35D1 SOX18 TSR2 UROD UROS

Diseases (30) :ORPHA:124 OMIM:608540 OMIM:618052 OMIM:618773 ORPHA:477774 OMIM:166210 OMIM:256540 ORPHA:137667 OMIM:617300 OMIM:153100 OMIM:153400 OMIM:265380 ORPHA:79277 OMIM:618838 OMIM:618839 OMIM:608013 OMIM:215140 OMIM:619313 OMIM:620014 OMIM:619003 OMIM:617049 OMIM:616843 OMIM:266200 OMIM:212065 OMIM:618835 OMIM:603830 OMIM:269250 OMIM:607823 OMIM:137940 ORPHA:95159
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is December 15 2022 release.