Global Variome shared LOVD

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

Phenotype #0000201823 Individual ID 00263964 Associated disease - Phenotype details inherited retinal degeneration (HP:0000546), retinal dystrophy (HP:0000556) Diagnosis/Initial - Inheritance Familial, autosomal recessive Diagnosis/Definite - Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Owner name Jasmine Chen Database submission license No license selected Created by Jasmine Chen Date created 2019-09-01 21:39:25 +02:00 (CEST) Date last edited 2019-09-13 12:57:55 +02:00 (CEST)

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