Disease #01237 (CTRCT41 (cataract, type 41 (CTRCT-41, congenital nuclear type)), OMIM:116400)

Official abbreviation CTRCT41
Name cataract, type 41 (CTRCT-41, congenital nuclear type)
OMIM ID 116400
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene WFS1
Associated tissues -
Disease features -
Remarks -