ZFIN Human Disease: primary autosomal recessive microcephaly 3

OBO ID: DOID:0070286

Term Name:	primary autosomal recessive microcephaly 3		Search Ontology:
Synonyms:	MCPH3
Definition:	A primary autosomal recessive microcephaly that has_material_basis_in homozygous or compound heterozygous mutation in the CDK5RAP2 gene on chromosome 9q33. https://www.ncbi.nlm.nih.gov/pubmed/15793586
References:	OMIM:604804
Ontology:	Human Disease ( DOID:0070286 )

Relationships

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

OTHER primary autosomal recessive microcephaly 3 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
CDK5RAP2	cdk5rap2	Microcephaly 3, primary, autosomal recessive	604804

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None