Phenotype #0000026561

Individual ID 00033132
Associated disease -
Phenotype details retinal degeneration, severe, early onset (EOSRD)
Diagnosis/Initial retinitis pigmentosa
Inheritance Unknown
Diagnosis/Definite -
Age/Examination 06y (6 years)
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Kornelia Neveling
Database submission license No license selected
Created by Kornelia Neveling
Date created 2012-02-04 14:23:49 +01:00 (CET)
Date last edited 2020-08-25 10:48:31 +02:00 (CEST)

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