Phenotype #0000201820

Individual ID 00263961
Associated disease -
Phenotype details retinitis pigmentosa (HP:0000510), field constriction (HP: 0007994), atrophy of retinal pigment epithelium (HP:0007722), high myopia (HP:0011003)
Diagnosis/Initial retinitis pigmentosa (RP)
Inheritance Familial, autosomal recessive
Diagnosis/Definite retinitis pigmentosa type 72 (RP-72)
Age/Examination 50y (50 years)
Age/Diagnosis 20y
Age/Onset 17y
Phenotype/Onset night blindness (HP:0000662), field constriction (HP:0007994)
Protein -
Owner name Jasmine Chen
Database submission license No license selected
Created by Jasmine Chen
Date created 2019-09-01 18:01:52 +02:00 (CEST)
Date last edited 2019-09-13 12:50:49 +02:00 (CEST)

Screenscraping/webscraping (interacting with LOVD using scripts to download data) is strictly prohibited.
Use our APIs to retrieve data.
  Powered by LOVD v.3.0 Build 30b
LOVD software ©2004-2024 Leiden University Medical Center
Database contents © by their respective submitters and curators
 There are currently no updates.