Disease #03026 (CTRCT33 (cataract, type 33 (CTRCT-33)), OMIM:611391)

Official abbreviation CTRCT33
Name cataract, type 33 (CTRCT-33)
OMIM ID 611391
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant, Autosomal recessive
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene BFSP1
Associated tissues -
Disease features -
Remarks -

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