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01 Keratoderma, Palmoplantar [NCBI]

Gene


 Gene Link Information
Gain		 01
LOC619540 [NCBI] 0.000415947
TYS [NCBI] 0.000415947
KWE [NCBI] 0.000355204
SLURP1 [NCBI] 0.000282676
KRT9 [NCBI] 0.00021133
GJB2 [NCBI] 0.000138843
KRT1 [NCBI] 9.95049e-05
DSP [NCBI] 7.55967e-05
LOR [NCBI] 6.23343e-05
KRT16 [NCBI] 5.74168e-05
DSG1 [NCBI] 3.11387e-05
SNAP29 [NCBI] 3.08332e-05
GJB3 [NCBI] 2.54934e-05
KRT14 [NCBI] 2.10187e-05
KRT6A [NCBI] 1.98583e-05
KRT17 [NCBI] 1.96727e-05
NPAL2 [NCBI] 1.54085e-05
KRT24 [NCBI] 1.54085e-05
KRTAP17-1 [NCBI] 1.54085e-05
KRT10 [NCBI] 1.5155e-05
GJB6 [NCBI] 1.44605e-05
GJA1 [NCBI] 1.40539e-05
ICHTHYIN [NCBI] 1.30282e-05
NIPA2 [NCBI] 1.15467e-05
RSPO1 [NCBI] 1.1113e-05
EDA [NCBI] 5.77981e-06
TGM1 [NCBI] 5.69832e-06
KRT5 [NCBI] 5.43407e-06
TAT [NCBI] 5.1943e-06
JUP [NCBI] 5.15942e-06
SOCS1 [NCBI] 4.86515e-06
SRY [NCBI] 4.67457e-06
ERCC2 [NCBI] 3.5246e-06
GJB1 [NCBI] 3.4916e-06



OMIM


 OMIM Link Information
gain		 01
TOC [NCBI] 0.00664234
AKE [NCBI] 0.00453294
keratosis palmoplantaris papulosa [NCBI] 0.00408847
schopf-schulz-passarge syndrome [NCBI] 0.0027297
keratosis, focal palmoplantar and gingival [NCBI] 0.00126183
PPPP [NCBI] 0.00119096
sclerotylosis [NCBI] 0.00113349
KRT9 [NCBI] 0.00112618
hypotrichosis-osteolysis-periodontitis-palmoplantar keratoderma syndrome [NCBI] 0.000892148
mal de meleda [NCBI] 0.000837895
EPPK [NCBI] 0.000810247
lelis syndrome [NCBI] 0.00067472
deafness, congenital, with keratopachydermia and constrictions of fingers and toes [NCBI] 0.000631717
naxos disease [NCBI] 0.000572723
tyrosine transaminase deficiency [NCBI] 0.000569468
keratolytic winter erythema [NCBI] 0.000540093
callosities, hereditary painful [NCBI] 0.000540093
keratosis palmoplantaris striata i [NCBI] 0.000510379
palmoplantar hyperkeratosis with squamous cell carcinoma of skin and sex reversal [NCBI] 0.000486331
SLURP1 [NCBI] 0.000460862
KRT1 [NCBI] 0.000423778
PC1 [NCBI] 0.000406423
cardiomyopathy, dilated, with woolly hair and keratoderma [NCBI] 0.000381132
porokeratosis of mibelli [NCBI] 0.000370612
HMS [NCBI] 0.000353185
keratoderma, palmoplantar, with deafness [NCBI] 0.000353185
keratoderma, palmoplantar, with nail dystrophy and hereditary motor-sensory neuropathy [NCBI] 0.000332002
GJB2 [NCBI] 0.000300128
PALS [NCBI] 0.000277542
vohwinkel syndrome, variant form [NCBI] 0.000264635
KRT16 [NCBI] 0.00025911
keratosis linearis with ichthyosis congenita and sclerosing keratoderma [NCBI] 0.000221166
hyperkeratosis-hyperpigmentation syndrome [NCBI] 0.000221166
NEPPK [NCBI] 0.000190229
knuckle pads, leukonychia, and sensorineural deafness [NCBI] 0.000166669
deafness, neural, with atypical atopic dermatitis [NCBI] 0.000166669
DPR [NCBI] 0.000159327
MTTS1 [NCBI] 0.000149178
SLE [NCBI] 0.000145442
DFNA3 [NCBI] 0.000144007
bullous erythroderma ichthyosiformis congenita of brocq [NCBI] 0.000136758
EBS-MP [NCBI] 0.000130884
KRT6A [NCBI] 0.00012545
keratosis palmoplantaris striata iii [NCBI] 0.0001105
cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome [NCBI] 0.0001105
mental retardation with spastic paraplegia and palmoplantar hyperkeratosis [NCBI] 0.0001105
keratoderma, palmoplantar, norrbotten recessive type [NCBI] 0.0001105
woolly hair, autosomal recessive [NCBI] 0.0001105
corneodermatoosseous syndrome [NCBI] 0.0001105
KRT17 [NCBI] 9.93004e-05
DSP [NCBI] 9.18588e-05
HFM [NCBI] 8.91667e-05
KRT14 [NCBI] 8.30184e-05
arthrogryposis and ectodermal dysplasia [NCBI] 7.95802e-05
mental retardation, buenos aires type [NCBI] 7.95802e-05
KRT15 [NCBI] 7.6426e-05
KRT24 [NCBI] 7.6426e-05
SNAP29 [NCBI] 7.6426e-05
DSG1 [NCBI] 7.5815e-05
OODD [NCBI] 7.40895e-05
naegeli syndrome [NCBI] 6.40681e-05
ichthyin [NCBI] 6.26498e-05
KRT13 [NCBI] 6.26498e-05
RSPO1 [NCBI] 6.26498e-05
IHCM [NCBI] 5.97481e-05
EDC [NCBI] 5.97481e-05
PC2 [NCBI] 5.97481e-05
blood group, p system [NCBI] 5.97481e-05
ED2 [NCBI] 4.81938e-05
keratitis-ichthyosis-deafness syndrome, autosomal dominant [NCBI] 4.81938e-05
JUP [NCBI] 4.79153e-05
BCNS [NCBI] 4.76687e-05
CIPA [NCBI] 4.64745e-05
RHS [NCBI] 4.56813e-05
LOR [NCBI] 4.52535e-05
KRT10 [NCBI] 4.316e-05
DAR [NCBI] 3.79489e-05
ODDD [NCBI] 3.70442e-05
KRT5 [NCBI] 3.33121e-05
costello syndrome [NCBI] 3.07135e-05
CRMO [NCBI] 2.78769e-05
SLS [NCBI] 2.45677e-05
IGFALS [NCBI] 2.33446e-05



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