Phenotype #0000291910

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Individual ID	00398815
Associated disease	CMT2O
Phenotype details	Demyelinating peripheral neuropathy (HP:0007108), Decreased nerve conduction velocity (HP:0000762)
Diagnosis/Initial	CMT
Inheritance	Familial, autosomal recessive
Diagnosis/Definite	-
Age/Examination	36y (36 years)
Age/Diagnosis	-
Age/Onset	34y
Phenotype/Onset	Demyelinating peripheral neuropathy (HP:0007108), Decreased nerve conduction velocity (HP:0000762)
Protein	-
Owner name	Yvet den Hartog
Database submission license
Created by	Yvet den Hartog
Date created	2022-01-13 12:35:15 +01:00 (CET)
Date last edited	2022-01-18 16:18:06 +01:00 (CET)

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