Phenotype #0000207993

Individual ID 00271386
Associated disease -
Phenotype details 10s-moderately severe rod-cone dystrophy; 36y-best corrected visual acuity right 20/200 and left counting finger, visual fields <10 degrees; fundus examination typical rod-cone dystrophy signs, atrophic macular changes, X-rays chest no situs inversus
Diagnosis/Initial retinitis pigmentosa
Inheritance Familial, autosomal recessive
Diagnosis/Definite RP82
Age/Examination 36y (36 years)
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2019-12-19 09:58:15 +01:00 (CET)
Date last edited N/A

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