Global Variome shared LOVD

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

Phenotype #0000201819 Individual ID 00263960 Associated disease - Phenotype details retinitis pigmentosa (HP:0000510), night blindness (HP:0000662), progressive loss of visual acuity (HP:0000529), photophobia (HP:0000613), visual field loss (HP:0007994), posterior subcapsular cataract (HP:0007787) Diagnosis/Initial retinitis pigmentosa (RP) Inheritance Familial, autosomal recessive Diagnosis/Definite retinitis pigmentosa type 72 (RP-72) Age/Examination 67y (67 years) Age/Diagnosis 50y Age/Onset 40y Phenotype/Onset night blindness (HP:0000662) Protein - Owner name Jasmine Chen Database submission license No license selected Created by Jasmine Chen Date created 2019-09-01 17:24:28 +02:00 (CEST) Date last edited 2019-09-13 12:43:06 +02:00 (CEST)

Screenscraping/webscraping (interacting with LOVD using scripts to download data) is strictly prohibited.
Use our APIs to retrieve data.