Phenotype #0000278930

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Individual ID	00385134
Associated disease	-
Phenotype details	HP:0008527 Congenital sensorineural hearing impairment; HP:0000545 Myopia; HP:0000662 Nyctalopia; HP:0000510 Rod-cone dystrophy
Diagnosis/Initial	Usher syndrome
Inheritance	Familial, autosomal recessive
Diagnosis/Definite	Usher syndrome
Age/Examination	5y1m (5 years, 1 month)
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Protein	-
Owner name	LOVD
Database submission license
Created by	Anna Tracewska
Date created	2021-10-08 17:29:22 +02:00 (CEST)
Date last edited	N/A

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