OBO ID: DOID:0070293
Term Name: primary autosomal recessive microcephaly 2 with or without cortical malformations Search Ontology:
Synonyms:
  • MCPH2
Definition: A primary autosomal recessive microcephaly that has_material_basis_in homozygous or compound heterozygous mutation in the WDR62 gene on chromosome 19q13. https://www.ncbi.nlm.nih.gov/pubmed/20890279
References:
Ontology: Human Disease   (DOID:0070293)
OTHER primary autosomal recessive microcephaly 2 with or without cortical malformations PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
WDR62 Microcephaly 2, primary, autosomal recessive, with or without cortical malformations 604317
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None