Fetal hydrops

Symptom Information:

Symptom ID: OMIM : No Id available
Synonyms:
Fetal hydrops (in perinatal or congenital neuromuscular forms) [OMIM:Fetal hydrops (in perinatal or congenital neuromuscular forms)]
Quality:
Cross references:
OMIM: "Fetal hydrops" [OMIM:Fetal hydrops]
OMIM: "Fetal hydrops (in perinatal or congenital neuromuscular forms)" [OMIM:Fetal hydrops (in perinatal or congenital neuromuscular forms)]
Is a (Direct Parents):
Is a (Whole tree): HPO:
MedDRA:
Database Frequency: 15 / 7739
Resource:

All diseases associated with this symptom:

Achondrogenesis type 1B (Orphanet:93298)
Achondrogenesis type 2 (Orphanet:93296)
BARTTER SYNDROME, TYPE 4A (OMIM:602522)
BARTTER SYNDROME, TYPE 4B (OMIM:613090)
CARDIAC VALVULAR DEFECT, DEVELOPMENTAL (OMIM:212093)
Cervicofacial lymphatic malformation (Orphanet:137923)
Cystic hygroma (Orphanet:79486)
Glycogen storage disease due to glycogen branching enzyme deficiency, adult neuromuscular form (Orphanet:308712)
Glycogen storage disease due to glycogen branching enzyme deficiency, childhood combined hepatic and myopathic form (Orphanet:308684)
Glycogen storage disease due to glycogen branching enzyme deficiency, childhood neuromuscular form (Orphanet:308698)
Glycogen storage disease due to glycogen branching enzyme deficiency, congenital neuromuscular form (Orphanet:308670)
Glycogen storage disease due to glycogen branching enzyme deficiency, fatal perinatal neuromuscular form (Orphanet:308655)
Glycogen storage disease due to glycogen branching enzyme deficiency, non progressive hepatic form (Orphanet:308638)
Glycogen storage disease due to glycogen branching enzyme deficiency, progressive hepatic form (Orphanet:308621)
Hypochondrogenesis (Orphanet:93297)