Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


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01 Dermoid Cyst [NCBI]


Gene


Gene Link Information
Gain
01
CND [NCBI] 0.000499621
PTCH1 [NCBI] 2.22962e-05
ESD [NCBI] 2.05328e-05
AFP [NCBI] 1.73745e-05
PTHLH [NCBI] 1.34735e-05
ERV3 [NCBI] 1.32509e-05
PITX2 [NCBI] 1.09396e-05
SALL1 [NCBI] 1.09396e-05
ENPP2 [NCBI] 1.01598e-05
GLI1 [NCBI] 9.42017e-06
IGFBP1 [NCBI] 8.48757e-06
GFAP [NCBI] 3.96868e-06




OMIM


OMIM Link Information
gain
01
CND [NCBI] 0.0032967
HFM [NCBI] 0.00194801
acromelic frontonasal dysostosis [NCBI] 0.000656414
schimmelpenning-feuerstein-mims syndrome [NCBI] 0.00051629
branchial clefts with characteristic facies, growth retardation, imperforate nasolacrimal duct, and premature aging [NCBI] 0.00051629
aplasia cutis congenita with epibulbar dermoids [NCBI] 0.000516235
RDC [NCBI] 0.000286357
ovarian teratoma [NCBI] 0.000241416
dermoid cysts, familial frontonasal [NCBI] 0.000142554
cleft, median, of upper lip with polyps of facial skin and nasal mucosa [NCBI] 9.87429e-05
PC2 [NCBI] 9.16802e-05
wildervanck syndrome [NCBI] 8.67829e-05
sacral defect with anterior meningocele [NCBI] 7.99881e-05
ORAOV1 [NCBI] 7.92643e-05
TBS [NCBI] 6.81149e-05
FGF3 [NCBI] 6.07361e-05
AFP [NCBI] 5.49972e-05
NRAS [NCBI] 5.46665e-05
PITX2 [NCBI] 5.093e-05
HMI [NCBI] 4.519e-05
SPINK1 [NCBI] 3.30638e-05
ACPP [NCBI] 2.45583e-05
PTHLH [NCBI] 2.16519e-05
CEACAM5 [NCBI] 1.8738e-05
GFAP [NCBI] 8.52534e-06




Database Center for Life Science