Phenotype #0000221712

Individual ID 00287979
Associated disease neuropathy, optic
Phenotype details Optic atrophy (HP:0000648); Seizures (HP:0001250); Memory impairment (HP:0002354)
Diagnosis/Initial -
Diagnosis/Definite -
Inheritance Familial, autosomal recessive
Age/Examination 30y (30 years)
Age/Diagnosis -
Age/Onset 04y
Phenotype/Onset -
Protein -
Owner name Khadidja Guehlouz
Database submission license No license selected
Created by Khadidja Guehlouz

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