Phenotype #0000210937

Individual ID	00276352
Associated disease	neuropathy, optic
Phenotype details	Congenital nystagmus (HP:0006934); Exotropia (HP:0000577); Migraine (HP:0002076); Scotoma (HP:0000575); Oculus dexter superonasal scotoma
Diagnosis/Initial	-
Diagnosis/Definite	-
Inheritance	Familial, autosomal dominant
Age/Examination	29y (29 years)
Age/Diagnosis	26y
Age/Onset	26y
Phenotype/Onset	-
Protein	-
Owner name	Khadidja Guehlouz
Database submission license	No license selected
Created by	Khadidja Guehlouz
Date created	2020-01-31 16:14:12 +01:00 (CET)
Date last edited	2020-08-25 21:27:59 +02:00 (CEST)

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