cataract 16 multiple types

Summary

DOID:0110250 - cataract 16 multiple types

Disease Ontology Definition:A cataract that has_material_basis_in heterozygous or homozygous mutation in the CRYAB gene on chromosome 11q.

Synonyms: CTPP2, CTRCT16, posterior polar cataract 2

Xenbase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: cryab

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0013411 - cranial cavity

MONDO:0013411 - cranial cavity

MIM:

MIM:613763 - CATARACT 16, MULTIPLE TYPES; CTRCT16

MIM:613763 - CATARACT 16, MULTIPLE TYPES; CTRCT16

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): autosomal dominant disease (is_a), autosomal recessive disease (is_a), cataract (is_a)