Condition: NEUROPATHY, CONGENITAL HYPOMYELINATING, 2


rs11154178 in LOC105377982;TRDN gene and NEUROPATHY, CONGENITAL HYPOMYELINATING, 2 PMID 28672053 2017 A genome-wide association study suggests that MAPK14 is associated with diabetic foot ulcers.

rs80028505 in MAPK14 gene and NEUROPATHY, CONGENITAL HYPOMYELINATING, 2 PMID 28672053 2017 A genome-wide association study suggests that MAPK14 is associated with diabetic foot ulcers.

rs3761980 in MAPK14;SLC26A8 gene and NEUROPATHY, CONGENITAL HYPOMYELINATING, 2 PMID 28672053 2017 A genome-wide association study suggests that MAPK14 is associated with diabetic foot ulcers.

rs121913595 in MPZ gene and NEUROPATHY, CONGENITAL HYPOMYELINATING, 2 PMID 15184631 2004 A novel MPZ gene mutation in congenital neuropathy with hypomyelination.

PMID 10319895 1999 Congenital hypomyelination due to myelin protein zero Q215X mutation.

PMID 8816708 1996 Clinical phenotypes of different MPZ (P0) mutations may include Charcot-Marie-Tooth type 1B, Dejerine-Sottas, and congenital hypomyelination.

rs28485846 in UNC5D gene and NEUROPATHY, CONGENITAL HYPOMYELINATING, 2 PMID 28672053 2017 A genome-wide association study suggests that MAPK14 is associated with diabetic foot ulcers.