microcephaly, primary autosomal recessive, 7

Preferred Label : microcephaly, primary autosomal recessive, 7;

Origin ID

C567198;

UMLS CUI

C2675187;

Automatic exact mappings (from CISMeF team)
- Microcephaly 7, primary, autosomal recessive [OMIM Phenotype]
- primary autosomal recessive microcephaly 7 [DO Concept]
MeSH term(s) associated for indexing
- microcephaly [MeSH Descriptor]
Record concept(s)
- microcephaly, primary autosomal recessive, 7 [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Microcephaly 7, primary, autosomal recessive [OMIM Phenotype]