ZFIN Human Disease: primary autosomal recessive microcephaly 7

OBO ID: DOID:0070278

Term Name:	primary autosomal recessive microcephaly 7		Search Ontology:
Synonyms:	MCPH7
Definition:	A primary autosomal recessive microcephaly that has_material_basis_in homozygous or compound heterozygous mutation in the STIL gene on chromosome 1p33. https://www.ncbi.nlm.nih.gov/pubmed/19215732
References:	OMIM:612703
Ontology:	Human Disease ( DOID:0070278 )

Relationships

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

OTHER primary autosomal recessive microcephaly 7 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
STIL	stil	Microcephaly 7, primary, autosomal recessive	612703

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None