Polyhydramnios, chronic idiopathic

Preferred Label : Polyhydramnios, chronic idiopathic;

Type : Other, mainly phenotypes with suspected mendelian basis;

Alternative titles and symbols : Lactogen receptor defect of chorion;

Inheritance : ? Autosomal recessive;

Prefixed ID : 263610;

Details

Origin ID

263610;

UMLS CUI

C1849720;

Currated CISMeF NLP mapping
- Chronic idiopathic polyhydramnios [HPO term]
- polyhydramnios, chronic idiopathic [MeSH concept]
- polyhydramnios, chronic idiopathic [MeSH Supplementary Concept]
HPO term(s)
- Autosomal recessive inheritance [HPO term]
- Chronic idiopathic polyhydramnios [HPO term]
- Polyhydramnios [HPO term]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Chronic idiopathic polyhydramnios [HPO term]
- polyhydramnios, chronic idiopathic [MeSH Supplementary Concept]
- polyhydramnios, chronic idiopathic [MeSH concept]

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