Disease #01341 (NMAN (neuromyotonia and axonal neuropathy, autosomal recessive (NMAN, Gamstorp-Wohlfart syndrome)), OMIM:137200)

Global Variome shared LOVD

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Official abbreviation	NMAN
Name	neuromyotonia and axonal neuropathy, autosomal recessive (NMAN, Gamstorp-Wohlfart syndrome)
OMIM ID	137200
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	HINT1
Associated tissues	-
Disease features	autosomal recessive
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	2021-12-10 21:51:32 +01:00 (CET)

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