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Metadata
ID	DOID:0110236
Name	cataract 39 multiple types
Definition	A cataract that has_material_basis_in heterozygous mutation in the CRYGB gene on chromosome 2q34. https://www.ncbi.nlm.nih.gov/pubmed/23288985
Xrefs	ICD10CM:Q12.0 OMIM:615188
Synonyms	autosomal dominant cataract 39 multiple types [EXACT] CTRCT39 [EXACT]
Parent Relationships	is_a cataract is_a autosomal dominant disease