Phenotype #0000201818

Individual ID 00263908
Associated disease -
Phenotype details retinitis pigmentosa (HP:0000510), night blindness (HP:0000662), retinal pigment epithelium atrophy (HP:0007791), photophobia (HP:0000613), visual field loss (HP:0007994), posterior subcapsular cataract (HP:0007787)
Diagnosis/Initial retinitis pigmentosa
Inheritance Familial, autosomal recessive
Diagnosis/Definite RP-72
Age/Examination 69y (69 years)
Age/Diagnosis 52y
Age/Onset 30y
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 17:11:34 +02:00 (CEST)
Date last edited 2019-09-13 12:35:09 +02:00 (CEST)

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