Brachial palsy, familial congenital

Preferred Label : Brachial palsy, familial congenital;

Type : Phenotype or locus, molecular basis unknown;

Prefixed ID : %608585;

Origin ID

608585;

UMLS CUI

C1837810;

Currated CISMeF NLP mapping
- brachial palsy, familial congenital [MeSH concept]
- brachial palsy, familial congenital [MeSH Supplementary Concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- brachial palsy, familial congenital [MeSH Supplementary Concept]
- brachial palsy, familial congenital [MeSH concept]