ZFIN Human Disease: primary autosomal recessive microcephaly 4

OBO ID: DOID:0070291

Term Name:	primary autosomal recessive microcephaly 4		Search Ontology:
Synonyms:	MCPH4
Definition:	A primary autosomal recessive microcephaly that has_material_basis_in homozygous or compound heterozygous mutation in the KNL1 gene on chromosome 15q15. https://www.ncbi.nlm.nih.gov/pubmed/22983954
References:	OMIM:604321
Ontology:	Human Disease ( DOID:0070291 )

Relationships

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

OTHER primary autosomal recessive microcephaly 4 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
KNL1	knl1	Microcephaly 4, primary, autosomal recessive	604321

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None