Gendoo

MeSH keywords -> Related genes, diseases (OMIM)

01	Dermoid Cyst	[NCBI]

Gene	Link	Information Gain
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	Link	Information gain
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