Phenotype #0000021234

Global Variome shared LOVD

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

Individual ID	00025020
Associated disease	CTRCT
Phenotype details	complete bilateral dense white autosomal recessive congenital cataract
Diagnosis/Initial	-
Inheritance	Familial, autosomal recessive
Diagnosis/Definite	-
Age/Examination	-
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Protein	-
Owner name	Inst.Human Genetics - Heidelberg
Database submission license	No license selected
Created by	Johan den Dunnen
Date created	2014-12-05 14:15:29 +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.