Disease #03773 (HMNR5;DSMA5 (neuronopathy, distal hereditary motor, autosomal recessive, type 5), OMIM:614881)

Global Variome shared LOVD

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Official abbreviation	HMNR5;DSMA5
Name	neuronopathy, distal hereditary motor, autosomal recessive, type 5
OMIM ID	614881
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	DNAJB2
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	2026-03-06 19:22:30 +01:00 (CET)

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