ZFIN Human Disease: primary autosomal recessive microcephaly 1

OBO ID: DOID:0070285

Term Name:	primary autosomal recessive microcephaly 1		Search Ontology:
Synonyms:	MCPH1
Definition:	A primary autosomal recessive microcephaly that has_material_basis_in homozygous or compound heterozygous mutation in the MCPH1 gene on chromosome 8p23. https://www.ncbi.nlm.nih.gov/pubmed/12046007
References:	OMIM:251200
Ontology:	Human Disease ( DOID:0070285 )

Relationships

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

OTHER primary autosomal recessive microcephaly 1 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
MCPH1	mcph1	Microcephaly 1, primary, autosomal recessive	251200

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None