ZFIN Human Disease: primary autosomal recessive microcephaly 9

OBO ID: DOID:0070292

Term Name:	primary autosomal recessive microcephaly 9		Search Ontology:
Synonyms:	MCPH9
Definition:	A primary autosomal recessive microcephaly that has_material_basis_in homozygous or compound heterozygous mutation in the CEP152 gene on chromosome 15q21. https://www.ncbi.nlm.nih.gov/pubmed/20598275
References:	OMIM:614852
Ontology:	Human Disease ( DOID:0070292 )

Relationships

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

OTHER primary autosomal recessive microcephaly 9 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
CEP152	cep152	Microcephaly 9, primary, autosomal recessive	614852

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None