Global Variome shared LOVD

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

Phenotype #0000027307 Individual ID 00033909 Associated disease CTRCT Phenotype details congenital; punctuate, nuclear, total; microcornea (1 individual) Diagnosis/Initial - Inheritance Familial, autosomal dominant Diagnosis/Definite - 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 2010-03-13 19:44:39 +01:00 (CET) Date last edited 2012-05-18 13:59:32 +02:00 (CEST)

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