MeSH keywords -> Related genes, diseases (OMIM)

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01 Hypertrichosis [NCBI]


Gene Link Information
ZLS [NCBI] 0.000401057
SLC29A3 [NCBI] 1.78315e-05
ERC2 [NCBI] 1.63495e-05
DSG4 [NCBI] 1.37888e-05
TRPS1 [NCBI] 1.28042e-05
NFATC2 [NCBI] 1.22717e-05
WNT5A [NCBI] 1.0857e-05
BAX [NCBI] 5.36597e-06
PRL [NCBI] 4.99688e-06
CDKN1A [NCBI] 4.54288e-06
EGFR [NCBI] 4.29194e-06


OMIM Link Information
HTC1 [NCBI] 0.00790396
hairy elbows [NCBI] 0.00700688
hypertrichotic osteochondrodysplasia [NCBI] 0.0056415
hypertrichosis universalis [NCBI] 0.00522772
HTC2 [NCBI] 0.00434534
ZLS [NCBI] 0.00227146
schinzel-giedion midface-retraction syndrome [NCBI] 0.00135739
fibromatosis, gingival, with progressive deafness [NCBI] 0.000643288
hairy ears, y-linked [NCBI] 0.000510346
acromegaloid facial appearance syndrome [NCBI] 0.000469828
fibromatosis, gingival, with hypertrichosis [NCBI] 0.000448448
hypertrichosis, anterior cervical [NCBI] 0.000382037
hypertrichosis, congenital anterior cervical, with peripheral sensory and motor neuropathy [NCBI] 0.000382037
barber-say syndrome [NCBI] 0.000327499
skin creases, multiple benign ring-shaped, of limbs [NCBI] 0.000314141
hairy ears [NCBI] 0.000209286
ramon syndrome [NCBI] 0.000192334
ablepharon-macrostomia syndrome [NCBI] 0.000176981
GINGF [NCBI] 0.000163813
donohue syndrome [NCBI] 0.000138802
hypertrichosis, hyperkeratosis, mental retardation, and distinctive facial features [NCBI] 0.000126878
growth deficiency and mental retardation with facial dysmorphism [NCBI] 0.000126878
cervical hypertrichosis with underlying kyphoscoliosis [NCBI] 0.000126878
cerebral malformation, seizures, hypertrichosis, and overlapping fingers [NCBI] 0.000126878
amaurosis congenita, cone-rod type, with congenital hypertrichosis [NCBI] 0.000126878
cahmr syndrome [NCBI] 0.000104412
fibromatosis, gingival, with hypertrichosis and mental retardation [NCBI] 0.000104412
mucopolysaccharidoses, unclassified types [NCBI] 9.59359e-05
gorlin-chaudhry-moss syndrome [NCBI] 9.59359e-05
LAH [NCBI] 9.0434e-05
DSG4 [NCBI] 6.8904e-05
PDP [NCBI] 6.18336e-05
MEN2B [NCBI] 5.44391e-05
mucopolysaccharidosis type vi [NCBI] 5.39542e-05
RA [NCBI] 5.3172e-05
porphyria cutanea tarda [NCBI] 5.05132e-05
porphyria variegata [NCBI] 4.10492e-05
alopecia, androgenetic [NCBI] 3.80355e-05
SHH [NCBI] 3.37864e-05
SLE [NCBI] 3.2963e-05
PRL [NCBI] 1.36424e-05
EGFR [NCBI] 1.17152e-05
CEACAM5 [NCBI] 1.00944e-05

Database Center for Life Science