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MeSH keywords -> Related genes, diseases (OMIM)


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01 Heredity [NCBI]


Gene


Gene Link Information
Gain
01
WNT4 [NCBI] 3.59125e-06
BRCA1 [NCBI] 2.76532e-06
MLH1 [NCBI] 2.57462e-06




OMIM


OMIM Link Information
gain
01
MRD [NCBI] 0.00134251
van bogaert-hozay syndrome [NCBI] 0.00119649
basilar impression, primary [NCBI] 0.000931631
spastic diplegia, infantile type [NCBI] 0.000931631
SHFM1 [NCBI] 0.000919553
acanthosis nigricans [NCBI] 0.000831882
ophthalmoplegia, familial static [NCBI] 0.000831882
CTPP1 [NCBI] 0.000719246
renal failure, progressive, with hypertension [NCBI] 0.000649401
RCD1 [NCBI] 0.000622333
DFN2 [NCBI] 0.000622333
TOC [NCBI] 0.000577767
telomere length, mean leukocyte [NCBI] 0.000541899
alport syndrome, autosomal dominant [NCBI] 0.00043447
HSAN2 [NCBI] 0.000170034
thumb, distal hyperextensibility of [NCBI] 0.000145111
OPCA V [NCBI] 0.000145111
cervical vertebral bridge [NCBI] 0.000145111
polyposis, intestinal, scattered and discrete [NCBI] 0.000145111
purpura simplex [NCBI] 0.000145111
calcification of joints and arteries [NCBI] 0.000145111
hypogonadism, male [NCBI] 0.000145111
VMD [NCBI] 0.000129127
osteogenesis imperfecta, type iia [NCBI] 0.000125537
SLS [NCBI] 0.000119223
ossified ear cartilages [NCBI] 0.000117351
cerebellar ataxia and ectodermal dysplasia [NCBI] 0.000117351
toe, misshapen [NCBI] 0.000117351
ichthyosis hystrix gravior [NCBI] 0.000117351
diabetes insipidus, neurohypophyseal type [NCBI] 0.000117351
keloids [NCBI] 0.000106882
syndactyly, type iii [NCBI] 0.000100089
ectopia lentis [NCBI] 0.000100089
CSCD [NCBI] 9.50405e-05
enchondromatosis, multiple [NCBI] 9.10207e-05
weill-marchesani syndrome, autosomal recessive [NCBI] 8.76801e-05
deafness, autosomal recessive [NCBI] 8.48224e-05
IHCM [NCBI] 8.23257e-05
elliptocytosis, rhesus-unlinked type [NCBI] 8.23257e-05
hydrocephalus [NCBI] 8.01092e-05
PFHB1A [NCBI] 7.81166e-05
OPPG [NCBI] 7.46497e-05
diabetes insipidus, nephrogenic, autosomal [NCBI] 7.31212e-05
pineal hyperplasia, insulin-resistant diabetes mellitus, and somatic abnormalities [NCBI] 7.31212e-05
MCPH1 [NCBI] 7.17031e-05
pituitary dwarfism iii [NCBI] 6.91419e-05
SCZD1 [NCBI] 6.91419e-05
pituitary dwarfism i [NCBI] 6.79769e-05
EL1 [NCBI] 6.58368e-05
donohue syndrome [NCBI] 6.39086e-05
CHNG2 [NCBI] 6.30118e-05
OCRL [NCBI] 6.13339e-05
RCDP1 [NCBI] 5.97899e-05
cystinuria [NCBI] 5.63977e-05
IGER [NCBI] 5.14902e-05
NPS [NCBI] 4.88075e-05
hypertrophic neuropathy of dejerine-sottas [NCBI] 4.83954e-05
maple syrup urine disease [NCBI] 4.75975e-05
CHM [NCBI] 4.60974e-05
TCOF [NCBI] 4.43784e-05
tritanopia [NCBI] 4.21584e-05
ALS1 [NCBI] 4.16392e-05
WT1 [NCBI] 3.58854e-05
OA1 [NCBI] 3.5289e-05
coproporphyria [NCBI] 3.51284e-05
giant platelet syndrome [NCBI] 3.48905e-05
SCZD [NCBI] 3.41337e-05
KIT [NCBI] 3.26924e-05
EV [NCBI] 3.23754e-05
factor v deficiency [NCBI] 3.03725e-05
INSR [NCBI] 2.7413e-05
adrenal hyperplasia, congenital, due to 21-hydroxylase deficiency [NCBI] 2.52674e-05
TS [NCBI] 1.00839e-05




Database Center for Life Science