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

Official abbreviation CTRCT-33
Name cataract, type 33 (CTRCT-33)
OMIM ID 611391
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene BFSP1
Associated tissues -
Disease features -
Remarks -