Disease #03007 (HMNR4;DSMA4 (neuronopathy, distal hereditary motor, autosomal recessive, type 4), OMIM:611067)

Global Variome shared LOVD

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Official abbreviation	HMNR4;DSMA4
Name	neuronopathy, distal hereditary motor, autosomal recessive, type 4
OMIM ID	611067
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	PLEKHG5
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	2026-03-06 19:20:50 +01:00 (CET)

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