Disease Details | GeDiPNet - Gene Disease Associations & Pathways

Disease Term	Disease ID	Gene Symbol	Classification	References	Source
NEUROPATHY, HEREDITARY MOTOR AND SENSORY, LOM TYPE	MESH:C535716	NDRG1	Unknown	—	CTD
NEUROPATHY, HEREDITARY MOTOR AND SENSORY, OKINAWA TYPE	604484 C1858338 MESH:C535717	TFG	Unknown	—	CTD Disgenet HPO
NEUROPATHY, HEREDITARY MOTOR AND SENSORY, RUSSE TYPE	605285 C1854449 MESH:C535813	HK1	Unknown	—	CTD Disgenet HPO
NEUROPATHY, HEREDITARY MOTOR AND SENSORY, TYPE 6A	MONDO:0011002	MFN2	Causal	—	ClinVar GenCC
NEUROPATHY, HEREDITARY MOTOR AND SENSORY, TYPE 6B	MONDO:0014671	SLC25A46	Causal	—	ClinGen ClinVar GenCC
NEUROPATHY, HEREDITARY MOTOR AND SENSORY, TYPE VIA, WITH OPTIC ATROPHY	601152	MFN2	Unknown	—	HPO
NEUROPATHY, HEREDITARY MOTOR AND SENSORY, TYPE VIB	C4225302	INF2	Unknown	—	Disgenet
		MFN2	Unknown	—	Disgenet
		SLC25A46	Unknown	—	Disgenet
NEUROPATHY, HEREDITARY MOTOR AND SENSORY, TYPE VIB, WITH OPTIC ATROPHY	616505 OMIM:616505	SLC25A46	Unknown	—	CTD HPO
NEUROPATHY, HEREDITARY MOTOR AND SENSORY, TYPE VIC, WITH OPTIC ATROPHY	618511 C5193137 MONDO:0032792	PDXK	Causal	31187503 32522499	CTD ClinVar Disgenet HPO

Hereditary motor and sensory neuropathy