Global Variome shared LOVD

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

Phenotype #0000201769 Individual ID 00263407 Associated disease - Phenotype details retinitis pigmentosa (HP:0000510), night blindness (HP:0000662), chorioretinal atrophy (HP:0000533) Diagnosis/Initial retinitis pigmentosa Inheritance Familial Diagnosis/Definite retinitis pigmentosa Age/Examination - Age/Diagnosis - Age/Onset 47y Phenotype/Onset night blindness (HP:0000662) Protein - Owner name Jasmine Chen Database submission license No license selected Created by Jasmine Chen Date created 2019-08-27 11:13:25 +02:00 (CEST) Date last edited 2020-08-25 10:48:31 +02:00 (CEST)

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