3 entries on 1 page. Showing entries 1 - 3.

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ID	Abbreviation	Name	OMIM ID	Individuals	Phenotypes	Associated with genes	Associated tissues	Disease features
00488	CMT2A2	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2A2; CMT2A2	609260	0	0	MFN2	-	-
00485	HSMN6	NEUROPATHY, HEREDITARY MOTOR AND SENSORY, TYPE VI; HSMN6	601152	0	0	MFN2	-	-
00494	MSL	LIPOMATOSIS, MULTIPLE SYMMETRIC; MSL	151800	0	0	MFN2	-	-

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