Arms, malformation of

Preferred Label : Arms, malformation of;

Type : Other, mainly phenotypes with suspected mendelian basis;

Inheritance : Autosomal dominant;

Prefixed ID : 107900;

Details

Origin ID

107900;

UMLS CUI

C1862534;

Automatic exact mappings (from CISMeF team)
- Arm deformity NOS [MedDRA LLT]
Currated CISMeF NLP mapping
- arms, malformation of [MeSH concept]
- arms, malformation of [MeSH Supplementary Concept]
HPO term(s)
- Autosomal dominant inheritance [HPO term]
- Hypoplasia of the radius [HPO term]
- Hypoplasia of the ulna [HPO term]
- Radioulnar synostosis [HPO term]
Semantic type(s)
- Congenital Abnormality [UMLS semantic type]
UMLS correspondences (same concept)
- arms, malformation of [MeSH Supplementary Concept]
- arms, malformation of [MeSH concept]

Keyword's position in hierarchy(ies) :

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