Disease #02342 (HMSN6A (neuropathyneuropathy, motor and sensory, hereditary, with optic atrophy, type6A (HMSN6A)), OMIM:601152)

Official abbreviation	HMSN6A
Name	neuropathyneuropathy, motor and sensory, hereditary, with optic atrophy, type6A (HMSN6A)
OMIM ID	601152
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	MFN2
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	2020-01-10 12:05:02 +01:00 (CET)

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Global Variome shared LOVD