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Metadata
ID DOID:0110242
Name cataract 13 with adult i phenotype
Definition A cataract that has_material_basis_in homozygous or compound heterozygous mutation in the GCNT2 gene on chromosome 6p24.
https://www.ncbi.nlm.nih.gov/pubmed/11739194
Xrefs

ICD10CM:Q12.0

MIM:116700

Synonyms

CTRCT13 [EXACT]

Parent Relationships

is_a cataract

is_a autosomal recessive disease

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