Global Variome shared LOVD

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

Phenotype #0000333397 Individual ID 00444143 Associated disease CTRCT Phenotype details see paper; ..., microcornea, psuedophakia, no coloboma, retinal detachment Diagnosis/Initial cataracts Inheritance Familial, autosomal dominant Diagnosis/Definite CTRCT2 Age/Examination - Age/Diagnosis - 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 2023-12-18 20:45:44 +01:00 (CET) Date last edited N/A

Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.