ZFIN Human Disease: primary autosomal recessive microcephaly 2 with or without cortical malformations

OBO ID: DOID:0070293

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:	OMIM:604317
Ontology:	Human Disease ( DOID:0070293 )

Relationships

is a type of:	primary autosomal recessive microcephaly primary autosomal recessive microcephaly Show first 5 Terms

OTHER primary autosomal recessive microcephaly 2 with or without cortical malformations PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
WDR62	wdr62	Microcephaly 2, primary, autosomal recessive, with or without cortical malformations	604317

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None