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MeSH keywords -> Related genes, diseases (OMIM)


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01 Geriatrics [NCBI]


Gene


Gene Link Information
Gain
01




OMIM


OMIM Link Information
gain
01
schimmelpenning-feuerstein-mims syndrome [NCBI] 0.000833714
neutropenia, chronic familial [NCBI] 0.000806417
scleroderma, familial progressive [NCBI] 0.000615577
hemophagocytic lymphohistiocytosis, familial, 1 [NCBI] 0.000528934
FSHMD1A [NCBI] 0.000346486
IDDM [NCBI] 0.000292453
HSAN1 [NCBI] 0.000174723
venular insufficiency, systemic [NCBI] 0.000153137
coracoclavicular joint, anomalous [NCBI] 0.000153137
atrial tachyarrhythmia with short pr interval [NCBI] 0.000153137
globulin anomaly involving beta (2a)-globulin [NCBI] 0.000153137
trigeminal neuralgia [NCBI] 0.000125373
anemia, autoimmune hemolytic [NCBI] 0.000114899
thymoma, familial [NCBI] 0.000114899
yellow nail syndrome [NCBI] 0.000108101
hypotension, orthostatic [NCBI] 0.000103048
hairy ears [NCBI] 0.000103048
hairy ears, y-linked [NCBI] 9.90237e-05
anonychia congenita [NCBI] 9.56784e-05
PDP [NCBI] 9.03146e-05
crigler-najjar syndrome, type ii [NCBI] 9.03146e-05
myeloma, multiple [NCBI] 8.6096e-05
PFHB1A [NCBI] 8.6096e-05
gilbert syndrome [NCBI] 7.96636e-05
coumarin resistance [NCBI] 7.83364e-05
mismatch repair cancer syndrome [NCBI] 7.27809e-05
CCAL2 [NCBI] 7.27809e-05
pulmonary fibrosis, idiopathic [NCBI] 7.18359e-05
TGD [NCBI] 7.09344e-05
osteoarthritis [NCBI] 6.84549e-05
lactase persistence [NCBI] 6.13732e-05
GLC1A [NCBI] 6.08411e-05
HYPP [NCBI] 6.08411e-05
VMD [NCBI] 5.83808e-05
HHT [NCBI] 5.57917e-05
RA [NCBI] 5.55631e-05
AHO [NCBI] 4.74381e-05
OPMD [NCBI] 4.20706e-05
SPTLC1 [NCBI] 3.73824e-05
PD [NCBI] 3.56968e-05
anemia, sideroblastic, x-linked [NCBI] 3.06829e-05
HS [NCBI] 2.83607e-05
PTH [NCBI] 2.74396e-05
CDH1 [NCBI] 2.74224e-05
MEN1 [NCBI] 2.48158e-05
MYOC [NCBI] 2.40068e-05
HBA1 [NCBI] 1.85958e-05
PI [NCBI] 1.82241e-05
ACE [NCBI] 1.54084e-05
FMF [NCBI] 1.46105e-05
BDNF [NCBI] 5.56996e-06
KLK3 [NCBI] 4.29626e-06
TNF [NCBI] 8.12468e-07
CRC [NCBI] 1.75962e-07




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