Disease #07241 (HMNR2;DSMA2 (neuronopathy, distal hereditary motor, autosomal recessive, type 2), OMIM:605726)

Global Variome shared LOVD

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Official abbreviation	HMNR2;DSMA2
Name	neuronopathy, distal hereditary motor, autosomal recessive, type 2
OMIM ID	605726
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	SIGMAR1
Associated tissues	-
Disease features	-
Remarks	-
Date created	2026-03-06 19:18:39 +01:00 (CET)
Date last edited	N/A

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