Global Variome shared LOVD

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

Phenotype #0000051968 Individual ID 00072263 Associated disease CCTRCT Phenotype details bilateral pseudophakia (HP:?), unremarkable retinal examination (HP:?) Diagnosis/Initial - Inheritance Familial, autosomal recessive Diagnosis/Definite - Age/Examination - Age/Diagnosis - Age/Onset 06y Phenotype/Onset - Protein - Owner name Jamie Zeegers Database submission license No license selected Created by Jamie Zeegers Date created 2016-06-03 10:05:49 +02:00 (CEST) Date last edited 2016-06-12 14:16:29 +02:00 (CEST)

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