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Metadata
ID DOID:0110241
Name cataract 41
Definition A cataract that has_material_basis_in heterozygous mutation in the WFS1 gene on chromosome 4p16.
https://www.ncbi.nlm.nih.gov/pubmed/23531866
Xrefs

ICD10CM:Q12.0

MIM:116400

Synonyms

congenital nuclear type cataract 41 [EXACT]

CTRCT41 [EXACT]

Parent Relationships

is_a autosomal dominant disease

is_a cataract

Subclass Logical Relationships

has material basis in some autosomal dominant inheritance

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