ZFIN Human Disease: cataract 11 multiple types

OBO ID: DOID:0110249

Term Name:	cataract 11 multiple types		Search Ontology:
Synonyms:	CPP4 CTPP4 CTRCT11 posterior polar cataract 4
Definition:	A cataract that has_material_basis_in heterozygous mutation in the PITX3 gene on chromosome 10q24. https://www.ncbi.nlm.nih.gov/pubmed/9620774
References:	ICD10CM:Q12.0 OMIM:610623
Ontology:	Human Disease ( DOID:0110249 )

Relationships

is a type of:	autosomal dominant disease autosomal recessive disease cataract autosomal dominant disease autosomal recessive disease cataract Show first 5 Terms

OTHER cataract 11 multiple types PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
PITX3	pitx3	Cataract 11, multiple types	610623
		Cataract 11, syndromic, autosomal recessive	610623

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None