Phenotype #0000291835

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Individual ID	00398752
Associated disease	CMT4B1
Phenotype details	Peripheral neuropathy (HP:0009830), No decreased nerve conduction velocity (-HP:0000762)
Diagnosis/Initial	CMT
Inheritance	Familial, autosomal recessive
Diagnosis/Definite	CMT4B1
Age/Examination	30y (30 years)
Age/Diagnosis	-
Age/Onset	22y
Phenotype/Onset	Peripheral neuropathy (HP:0009830), No decreased nerve conduction velocity (-HP:0000762)
Protein	-
Owner name	Yvet den Hartog
Database submission license
Created by	Yvet den Hartog
Date created	2022-01-11 15:52:54 +01:00 (CET)
Date last edited	2022-01-18 16:07:41 +01:00 (CET)

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