Phenotype #0000310090

Individual ID	00418793
Associated disease	neuropathy, optic
Phenotype details	Optic atrophy (HP:0000648); Optic neuropathy (HP:0001138); Reduced visual acuity (HP:0007663); Red-green dyschromatopsia (HP:0000642); Nystagmus (HP:0000639); Abnormality of visual evoked potentials (HP:0000649)
Diagnosis/Initial	-
Diagnosis/Definite	-
Inheritance	Familial, autosomal dominant
Age/Examination	38y (38 years)
Age/Diagnosis	-
Age/Onset	06y
Phenotype/Onset	-
Protein	-
Owner name	Mohamed Selhane
Database submission license
Created by	Mohamed Selhane
Date created	2022-10-07 09:49:22 +02:00 (CEST)
Date last edited	2024-07-18 13:20:45 +02:00 (CEST)

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