Disease #03301 (CMT2N (Charcot-Marie-Tooth disease, type 2N (CMT2N)), OMIM:613287)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	CMT2N
Name	Charcot-Marie-Tooth disease, type 2N (CMT2N)
OMIM ID	613287
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	AARS
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	2020-02-02 17:08:05 +01:00 (CET)

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