Global Variome shared LOVD

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

Phenotype #0000061169 Individual ID 00065073 Associated disease CTRCT Phenotype details congenital cataract, microcornea Diagnosis/Initial cataract Inheritance Familial, autosomal dominant Diagnosis/Definite CTRCT1 Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Owner name Deepti Anand Database submission license No license selected Created by Johan den Dunnen Date created 2016-10-18 12:03:27 +02:00 (CEST) Date last edited 2023-03-20 09:46:53 +01:00 (CET)

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