Global Variome shared LOVD

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

Phenotype #0000027276 Individual ID 00033878 Associated disease CTRCT Phenotype details microcornea; posterior polar progressing to dense nuclear/laminar, involvement anterior/posterior poles; congenital nystagmus Diagnosis/Initial cataract Inheritance Familial, autosomal dominant Diagnosis/Definite CTRCT9 Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Owner name Lars Hansen Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International Created by Lars Hansen Date created 2010-11-28 15:08:46 +01:00 (CET) Date last edited 2023-03-19 17:36:13 +01:00 (CET)

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