Global Variome shared LOVD

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

Phenotype #0000021235 Individual ID 00025118 Associated disease CTRCT Phenotype details complete bilateral dense white autosomal recessive congenital cataract Diagnosis/Initial - Inheritance Familial, autosomal recessive Diagnosis/Definite - Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Owner name Inst.Human Genetics - Heidelberg Database submission license No license selected Created by Johan den Dunnen Date created 2014-12-05 14:35:22 +01:00 (CET) Date last edited N/A

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