Phenotype #0000210620

Individual ID 00276063
Associated disease neuropathy, optic
Phenotype details Macular dystrophy (HP:0007754); Optic atrophy (HP:0000648)
Diagnosis/Initial -
Diagnosis/Definite -
Inheritance Familial, autosomal dominant
Age/Examination 30y (30 years)
Age/Diagnosis 30y
Age/Onset 13y
Phenotype/Onset -
Protein -
Owner name Khadidja Guehlouz
Database submission license No license selected
Created by Khadidja Guehlouz
Date created 2020-01-24 13:35:25 +01:00 (CET)
Date last edited 2020-08-25 21:27:59 +02:00 (CEST)

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