Phenotype #0000242743

Global Variome shared LOVD

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

Individual ID	00324162
Associated disease	CORD5
Phenotype details	macular degeneration (HP:0000608), progressive visual loss (HP:0000529), color vision defect (HP:0000551)
Diagnosis/Initial	cone-rod dystrophy
Inheritance	Familial, autosomal dominant
Diagnosis/Definite	CORD5
Age/Examination	32y (32 years)
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Protein	-
Owner name	Mariah De Bruin
Database submission license	No license selected
Created by	Mariah De Bruin
Date created	2020-12-03 10:55:35 +01:00 (CET)
Date last edited	2020-12-11 10:05:39 +01:00 (CET)

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