Disease #06529 (HMSN6C (Neuropathy, hereditary motor and sensory, type VIC, with optic atrophy), OMIM:618511)

Global Variome shared LOVD

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Official abbreviation	HMSN6C
Name	Neuropathy, hereditary motor and sensory, type VIC, with optic atrophy
OMIM ID	618511
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	PDXK
Associated tissues	-
Disease features	-
Remarks	-
Date created	2021-12-10 23:20:41 +01:00 (CET)
Date last edited	N/A

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