Global Variome shared LOVD

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

Phenotype #0000052817 Individual ID 00073138 Associated disease CCTRCT Phenotype details severe bilateral lamellar cataract (HP:0007971) Diagnosis/Initial - Inheritance Familial, autosomal dominant Diagnosis/Definite - Age/Examination - Age/Diagnosis 04y Age/Onset - Phenotype/Onset - Protein - Owner name Jamie Zeegers Database submission license No license selected Created by Jamie Zeegers Date created 2016-06-08 12:00:02 +02:00 (CEST) Date last edited 2017-07-11 21:55:43 +02:00 (CEST)

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