Disease #03723 (HMND12 (neuronopathy, distal hereditary motor, autosomal dominant, type 12), OMIM:620011)

Official abbreviation	HMND12
Name	neuronopathy, distal hereditary motor, autosomal dominant, type 12
OMIM ID	620011
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	REEP1
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	2026-03-06 19:32:49 +01:00 (CET)

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Global Variome shared LOVD