Global Variome shared LOVD

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

Phenotype #0000324399 Individual ID 00434020 Associated disease CTRCT Phenotype details congenital hereditary nuclear cataract; axial myopia, amblyopia, concomitant strabismus, lower eyelid tum(Entropon); visual acuity 0.7/0.5 Diagnosis/Initial cataract Inheritance Familial, autosomal dominant Diagnosis/Definite CTRCT5 Age/Examination - Age/Diagnosis 3y Age/Onset - Phenotype/Onset - Protein - Owner name Johan den Dunnen Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International Created by Johan den Dunnen Date created 2023-03-17 16:18:55 +01:00 (CET) Date last edited N/A

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