Phenotype #0000130129

Individual ID	00165250
Associated disease	MGR1
Phenotype details	The patient had ERDB. Episodes occurred up to 15 times per day and were a significant handicap. Frequent falls and brief episodes of disconnection (because of blindness) at age 4 years. Since age 7 years, she has had FHM.
Diagnosis/Initial	FHM
Inheritance	-
Diagnosis/Definite	FHM-3
Age/Examination	-
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Protein	-
Owner name	Paola Carrera
Database submission license	No license selected
Created by	Paola Carrera
Date created	2012-07-25 13:46:30 +02:00 (CEST)
Date last edited	2018-07-06 17:15:19 +02:00 (CEST)

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