ZFIN Human Disease: primary autosomal recessive microcephaly 11

OBO ID: DOID:0070287

Term Name:	primary autosomal recessive microcephaly 11		Search Ontology:
Synonyms:	MCPH11
Definition:	A primary autosomal recessive microcephaly that has_material_basis_in homozygous or compound heterozygous mutation in the PHC1 gene on chromosome 12p13. https://www.ncbi.nlm.nih.gov/pubmed/23418308
References:	OMIM:615414
Ontology:	Human Disease ( DOID:0070287 )

Relationships

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

OTHER primary autosomal recessive microcephaly 11 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
PHC1	phc1	?Microcephaly 11, primary, autosomal recessive	615414

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None