Disease #01234 (CTRCT20 (cataract, type 20 (CTRCT-20, membranous)), OMIM:116100)

Official abbreviation CTRCT20
Name cataract, type 20 (CTRCT-20, membranous)
OMIM ID 116100
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene CRYGS
Associated tissues -
Disease features -
Remarks -

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