Phenotype #0000221715

Individual ID	00287982
Associated disease	neuropathy, optic
Phenotype details	Nystagmus (HP:0000639); Ataxia (HP:0001251); Abnormal cerebellum morphology (HP:0001317); Peripheral neuropathy (HP:0009830); Dysarthria (HP:0001260)
Diagnosis/Initial	-
Diagnosis/Definite	-
Inheritance	Familial, autosomal recessive
Age/Examination	61y (61 years)
Age/Diagnosis	-
Age/Onset	30y
Phenotype/Onset	-
Protein	-
Owner name	Khadidja Guehlouz
Database submission license	No license selected
Created by	Khadidja Guehlouz
Date created	2020-02-14 20:40:52 +01:00 (CET)
Date last edited	2020-06-20 13:06:19 +02:00 (CEST)

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