Disease #02372 (CTRCT3 (cataract, type 3 (CTRCT-3)), OMIM:601547)

Official abbreviation CTRCT3
Name cataract, type 3 (CTRCT-3)
OMIM ID 601547
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene CRYBB2
Associated tissues -
Disease features -
Remarks -