hypospadias 3, autosomal

Preferred Label : hypospadias 3, autosomal;

Origin ID

C567191;

UMLS CUI

C2675154;

Currated CISMeF NLP mapping
- Hypospadias 3, autosomal [OMIM Phenotype]
MeSH term(s) associated for indexing
- hypospadias [MeSH Descriptor]
Record concept(s)
- hypospadias 3, autosomal [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Hypospadias 3, autosomal [OMIM Phenotype]