ZFIN Human Disease: primary autosomal recessive microcephaly 12

OBO ID: DOID:0070284

Term Name:	primary autosomal recessive microcephaly 12		Search Ontology:
Synonyms:	MCPH12
Definition:	A primary autosomal recessive microcephaly that has_material_basis_in homozygous or compound heterozygous mutation in the CDK6 gene on chromosome 7q21. https://www.ncbi.nlm.nih.gov/pubmed/23918663
References:	OMIM:616080
Ontology:	Human Disease ( DOID:0070284 )

Relationships

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

OTHER primary autosomal recessive microcephaly 12 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
CDK6	cdk6	?Microcephaly 12, primary, autosomal recessive	616080

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None