Nonimmune hydrops fetalis

Symptom Information:

Symptom ID: HPO:0001790
Synonyms:
Hydrops fetalis, non-immune [HPO:0001790]
Hydrops fetalis, nonimmune [HPO:0001790]
Non-immune fetal hydrops [HPO:0001790]
Nonimmune hydrops [HPO:0001790]
Hydrops fetalis, non-immune [OMIM:Hydrops fetalis, non-immune]
Hydrops fetalis, nonimmune [OMIM:Hydrops fetalis, nonimmune]
Nonimmune hydrops [OMIM:Nonimmune hydrops]
Nonimmune hydrops fetalis [OMIM:Nonimmune hydrops fetalis]
Hydrops fetalis, non-immune (rare) [OMIM:Hydrops fetalis, non-immune (rare)]
Non-immune fetal hydrops (rare) [OMIM:Non-immune fetal hydrops (rare)]
Quality:
Cross references:
OMIM: "Hydrops fetalis, non-immune" [OMIM:Hydrops fetalis, non-immune]
OMIM: "Hydrops fetalis, nonimmune" [OMIM:Hydrops fetalis, nonimmune]
OMIM: "Nonimmune hydrops" [OMIM:Nonimmune hydrops]
OMIM: "Nonimmune hydrops fetalis" [OMIM:Nonimmune hydrops fetalis]
OMIM: "Hydrops fetalis, non-immune (rare)" [OMIM:Hydrops fetalis, non-immune (rare)]
OMIM: "Non-immune fetal hydrops (rare)" [OMIM:Non-immune fetal hydrops (rare)]
Is a (Direct Parents):
HPO         Hydrops fetalis
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of prenatal development or birth(HPO:0001197)
          Hydrops fetalis(HPO:0001789)
             Nonimmune hydrops fetalis(HPO:0001790)
       Abnormality of metabolism/homeostasis(HPO:0001939)
          Abnormality of fluid regulation(HPO:0011032)
             Edema(HPO:0000969)
                Hydrops fetalis(HPO:0001789)
                   Nonimmune hydrops fetalis(HPO:0001790)
MedDRA:
Database Frequency: 15 / 7739
Resource:

All diseases associated with this symptom:

ALG1-CDG (Orphanet:79327)
Congenital pulmonary lymphangiectasia (Orphanet:2414)
Fetal Gaucher disease (Orphanet:85212)
Gaucher disease type 2 (Orphanet:77260)
Greenberg dysplasia (Orphanet:1426)
HYDROPS FETALIS, NONIMMUNE, WITH GRACILE BONES AND DYSMORPHIC FEATURES (OMIM:613124)
Hemolytic anemia due to red cell pyruvate kinase deficiency (Orphanet:766)
Hypotrichosis - lymphedema - telangiectasia (Orphanet:69735)
LYMPHEDEMA, HEREDITARY, IA (OMIM:153100)
Milroy disease (Orphanet:79452)
Neonatal hemochromatosis (Orphanet:446)
OSTEOGENESIS IMPERFECTA, TYPE II (OMIM:166210)
Osteogenesis imperfecta type 2 (Orphanet:216804)
PMM2-CDG (Orphanet:79318)
Psychomotor retardation due to S-adenosylhomocysteine hydrolase deficiency (Orphanet:88618)