ZFIN Human Disease: cataract 16 multiple types

OBO ID: DOID:0110250

Term Name:	cataract 16 multiple types		Search Ontology:
Synonyms:	CTPP2 CTRCT16 posterior polar cataract 2
Definition:	A cataract that has_material_basis_in heterozygous or homozygous mutation in the CRYAB gene on chromosome 11q. https://www.ncbi.nlm.nih.gov/pubmed/11577372
References:	ICD10CM:Q12.0 OMIM:613763
Ontology:	Human Disease ( DOID:0110250 )

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 16 multiple types PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
CRYAB	cryaba cryabb	Cataract 16, multiple types	613763

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None