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.