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MeSH keywords -> Related genes, diseases (OMIM)


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01 Hyalin [NCBI]

Gene


 Gene Link Information
Gain		 01
LOC619511 [NCBI] 0.000582873
ANTXR2 [NCBI] 5.52897e-05
SOD1 [NCBI] 3.42726e-05
CD68 [NCBI] 2.17349e-05
MYH7 [NCBI] 1.74958e-05
CILP [NCBI] 1.37328e-05
AFP [NCBI] 1.2951e-05
CDSN [NCBI] 1.28477e-05
SQSTM1 [NCBI] 1.05566e-05
ACP5 [NCBI] 9.98797e-06
COMP [NCBI] 8.79159e-06
CD99 [NCBI] 8.67349e-06
UMOD [NCBI] 7.50792e-06
CREB3L1 [NCBI] 6.91559e-06
MIB1 [NCBI] 5.85575e-06
CCS [NCBI] 5.81573e-06
ANKH [NCBI] 5.60438e-06
ANTXR1 [NCBI] 5.37809e-06
LRP6 [NCBI] 5.15254e-06
MKI67 [NCBI] 4.98565e-06
NR4A3 [NCBI] 4.9357e-06
SPAST [NCBI] 4.90374e-06
ADFP [NCBI] 4.85764e-06
ATXN2 [NCBI] 4.75773e-06
DMBT1 [NCBI] 4.7178e-06
YWHAB [NCBI] 4.45557e-06
ATXN3 [NCBI] 4.1627e-06
MYOG [NCBI] 4.01731e-06
TBP [NCBI] 3.93106e-06
PCNA [NCBI] 3.80186e-06
MITF [NCBI] 3.52575e-06
MYOD1 [NCBI] 3.32194e-06
PKD1 [NCBI] 3.2516e-06
NID1 [NCBI] 3.19153e-06
MATN1 [NCBI] 3.17503e-06
FGFR3 [NCBI] 3.15613e-06
CNN1 [NCBI] 3.01226e-06
VHL [NCBI] 2.94764e-06
GJB2 [NCBI] 2.90548e-06
TG [NCBI] 2.46035e-06
BMP2 [NCBI] 1.90849e-06
GFAP [NCBI] 1.05675e-06
PTGS2 [NCBI] 1.03511e-06
CASP3 [NCBI] 6.89298e-07



OMIM


 OMIM Link Information
gain		 01
lobular glomerulopathy, familial [NCBI] 0.00145218
myopathy, hyaline body, autosomal recessive [NCBI] 0.00133487
CGF [NCBI] 0.00125871
stiff skin syndrome [NCBI] 0.0011195
fibromatosis, juvenile hyaline [NCBI] 0.000737715
hyalinosis, infantile systemic [NCBI] 0.00060509
myopathy, myosin storage [NCBI] 0.000495806
lipoid proteinosis of urbach and wiethe [NCBI] 0.000456264
ichthyosis vulgaris [NCBI] 0.000296732
ichthyosis hystrix gravior [NCBI] 0.000182229
glomerulonephritis with sparse hair and telangiectases [NCBI] 0.000167415
IHCM [NCBI] 0.000150651
winchester syndrome [NCBI] 0.000150651
epidermolysis bullosa dystrophica, pasini type [NCBI] 0.000140224
macular dystrophy, vitelliform, adult-onset [NCBI] 0.000140224
white sponge nevus of cannon [NCBI] 0.000136174
CDGG1 [NCBI] 0.000126664
ichthyosis congenita, harlequin fetus type [NCBI] 0.000117558
SOD1 [NCBI] 0.000115387
MYH7 [NCBI] 0.000115161
mucolipidosis iiia [NCBI] 0.000112262
bullous erythroderma ichthyosiformis congenita of brocq [NCBI] 9.32174e-05
ABL [NCBI] 9.08882e-05
ALS1 [NCBI] 8.43018e-05
mucolipidosis ii [NCBI] 7.99807e-05
AFP [NCBI] 6.23138e-05
CREB3L2 [NCBI] 5.02988e-05
COMP [NCBI] 4.74661e-05
ANTXR2 [NCBI] 4.6034e-05
CCS [NCBI] 4.23486e-05
farber lipogranulomatosis [NCBI] 3.99257e-05
MMP14 [NCBI] 3.99257e-05
MTP [NCBI] 3.9271e-05
FUS [NCBI] 3.58526e-05
PRPH2 [NCBI] 3.41342e-05
ENPEP [NCBI] 2.78482e-05
RA [NCBI] 2.69421e-05
TNC [NCBI] 2.20558e-05
MUC1 [NCBI] 1.34007e-05
PCNA [NCBI] 1.30091e-05
ACP5 [NCBI] 1.14222e-05
TG [NCBI] 1.00977e-05
SLE [NCBI] 6.96067e-06
CEACAM5 [NCBI] 4.39353e-06
CRH [NCBI] 2.11218e-06
GFAP [NCBI] 1.6276e-06
VEGF [NCBI] 4.11536e-08



Database Center for Life Science