Phenotype #0000038135

Global Variome shared LOVD

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

	Curator: Global Variome, with Curator vacancy

Individual ID	00051532
Associated disease	BCS2
Phenotype details	see paper, brittel cornea syndrome, ...
Diagnosis/Initial	-
Inheritance	Familial, autosomal recessive
Diagnosis/Definite	-
Age/Examination	-
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Protein	-
Owner name	Shazia Micheal
Database submission license	No license selected
Created by	Johan den Dunnen
Date created	2015-10-02 21:56:52 +02:00 (CEST)
Date last edited	2017-11-29 08:07:01 +01:00 (CET)

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