Phenotype #0000201906

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Individual ID	00264053
Associated disease	-
Phenotype details	retinitis pigmentosa (HP:0000510), high myopia (HP:0011003), cataract (HP:0000518)
Diagnosis/Initial	retinitis pigmentosa (RP)
Inheritance	Familial, autosomal recessive
Diagnosis/Definite	retinitis pigmentosa type 72 (RP-72)
Age/Examination	40y (40 years)
Age/Diagnosis	-
Age/Onset	30y
Phenotype/Onset	nyctalopia (HP:0000662)
Protein	-
Owner name	Jasmine Chen
Database submission license	No license selected
Created by	Jasmine Chen
Date created	2019-09-08 21:08:45 +02:00 (CEST)
Date last edited	2019-09-13 13:12:49 +02:00 (CEST)

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