Phenotype #0000334282

Global Variome shared LOVD

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

Individual ID	00445029
Associated disease	CTRCT
Phenotype details	bilateral nuclear cataract, microphthalmos, no ocular/systemic problems
Diagnosis/Initial	cataract
Inheritance	Familial, autosomal dominant
Diagnosis/Definite	CTRCT22
Age/Examination	00y03m (3 months)
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Protein	-
Owner name	Johan den Dunnen
Database submission license
Created by	Johan den Dunnen
Date created	2023-12-31 10:16:57 +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.