Microcephaly 29, primary, autosomal recessive

Preferred Label : Microcephaly 29, primary, autosomal recessive;

Symbol : MCPH29;

Type : Phenotype, molecular basis known;

Prefixed ID : #620047;

Details

Origin ID

620047;

UMLS CUI

C5774220;

Genes related to phenotype
- Programmed cell death 6-interacting protein [OMIM gene]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

Keyword's position in hierarchy(ies) :

You can consult :

All resources
or only the major
or use the search engine

recommendations
documents concerning education
documents for patients