Disease #02873 (CTRCT22;CATCN2 (cataract, type 22 (CTRCT-22, cataract congenital nuclear, autosomal recessive 2 CATCN-2))), OMIM:609741)

Official abbreviation CTRCT22;CATCN2
Name cataract, type 22 (CTRCT-22, cataract congenital nuclear, autosomal recessive 2 CATCN-2))
OMIM ID 609741
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 CRYBB3
Associated tissues -
Disease features -
Remarks -