Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ] Register as submitter | Log in

Phenotype #0000275992 Individual ID 00382150 Associated disease CTRCT6 Phenotype details congenital cataract; MIM, 116600 Diagnosis/Initial MIM, 116600 Inheritance Familial, autosomal dominant Diagnosis/Definite - Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Owner name LOVD Database submission license Creative Commons Attribution 4.0 International Created by Anna Tracewska Date created 2021-09-07 10:12:12 +02:00 (CEST) Date last edited N/A

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