Global Variome shared LOVD

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

Phenotype #0000051162 Individual ID 00065010 Associated disease CTRCT Phenotype details congenital cataract, vitreoretinal dysplasia, neurodevelopmental delay, joint laxity Diagnosis/Initial - Inheritance Unknown Diagnosis/Definite - 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 2016-05-15 14:36:57 +02:00 (CEST) Date last edited N/A

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