cataract 21 multiple types

Summary

DOID:0110256 - cataract 21 multiple types

Disease Ontology Definition:A cataract that has_material_basis_in heterozygous mutation in the MAF gene on chromosome 16q23.

Synonyms: cataract 21 multiple types with or without microcornea, CCA4, congenital cataract Cerulean type 4, CTRCT21

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

: maf

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0012437 - epithelial-mesenchymal boundary

MONDO:0012437 - epithelial-mesenchymal boundary

MIM:

MIM:610202 - CATARACT 21, MULTIPLE TYPES; CTRCT21

MIM:610202 - CATARACT 21, MULTIPLE TYPES; CTRCT21

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), cataract (is_a)