Phenotype #0000054297

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Individual ID	00074490
Associated disease	CORD
Inheritance	Familial, autosomal recessive
Diagnosis/Initial	-
Age/Examination	-
Diagnosis/Definite	-
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Phenotype details	see paper; ..., diagnoised with CORD+SNHL (cone-rod degeneration with sensorineural hearing loss)
Protein	-
Owner name	Prasanthi Namburi
Database submission license	No license selected
Created by	Prasanthi Namburi
Date created	2016-07-05 09:10:35 +02:00 (CEST)
Date last edited	2020-08-28 17:29:39 +02:00 (CEST)

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