Disease #05616 (CMT2DD (Charcot-Marie-Tooth disease, axonal, type 2DD (CMT-2DD)), OMIM:618036)

Official abbreviation	CMT2DD
Name	Charcot-Marie-Tooth disease, axonal, type 2DD (CMT-2DD)
OMIM ID	618036
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	ATP1A1
Associated tissues	-
Disease features	autosomal dominant
Remarks	-
Date created	2019-06-28 15:10:07 +02:00 (CEST)
Date last edited	2021-12-10 21:51:32 +01:00 (CET)

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Global Variome shared LOVD