Phenotype #0000321077

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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	Curator: Global Variome, with Curator vacancy

Individual ID	00430268
Associated disease	CMT2T
Phenotype details	-
Diagnosis/Initial	-
Inheritance	Familial, autosomal dominant
Diagnosis/Definite	-
Age/Examination	66
Age/Diagnosis	-
Age/Onset	50y?
Phenotype/Onset	walking difficulties
Protein	-
Owner name	Marco Savarese
Database submission license
Created by	Marco Savarese
Date created	2023-01-16 16:30:30 +01:00 (CET)
Date last edited	2023-01-17 12:00:41 +01:00 (CET)

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