ZFIN Human Disease: primary autosomal recessive microcephaly 10

OBO ID: DOID:0070294

Term Name:	primary autosomal recessive microcephaly 10		Search Ontology:
Synonyms:	MCPH10
Definition:	A primary autosomal recessive microcephaly that has_material_basis_in homozygous or compound heterozygous mutation in the ZNF335 gene on chromosome 20q13. https://www.ncbi.nlm.nih.gov/pubmed/23178126
References:	OMIM:615095
Ontology:	Human Disease ( DOID:0070294 )

Relationships

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

OTHER primary autosomal recessive microcephaly 10 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
ZNF335	znf335	Microcephaly 10, primary, autosomal recessive	615095

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None