Global Variome shared LOVD

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

Phenotype #0000046582 Individual ID 00060092 Associated disease CTRCT Phenotype details - Diagnosis/Initial cataract Inheritance Familial, autosomal dominant Diagnosis/Definite CTRCT1 Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Owner name Johan den Dunnen Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International Created by Johan den Dunnen Date created 2011-11-17 23:11:29 +01:00 (CET) Date last edited 2023-03-20 09:30:48 +01:00 (CET)

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