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01 Anthropometry [NCBI]

Gene


 Gene Link Information
Gain		 01



OMIM


 OMIM Link Information
gain		 01
IS1 [NCBI] 0.0037056
apnea, obstructive sleep [NCBI] 0.00209429
PWS [NCBI] 0.000734788
dysosteosclerosis [NCBI] 0.000705429
ocular hypotelorism, submucosal cleft palate, and hypospadias [NCBI] 0.000705429
CF [NCBI] 0.000698484
CFM1 [NCBI] 0.000606521
bone size quantitative trait locus 1 [NCBI] 0.000606521
metatropic dwarfism [NCBI] 0.000606521
FPLD1 [NCBI] 0.000542709
pulmonary function [NCBI] 0.000542709
asperger syndrome, susceptibility to, 1 [NCBI] 0.000542709
CMDR [NCBI] 0.000495567
SHBG [NCBI] 0.000479467
short rib-polydactyly syndrome, type i [NCBI] 0.000458242
pygmy [NCBI] 0.000340329
SLE [NCBI] 0.000290422
abdominal obesity-metabolic syndrome [NCBI] 0.000250944
ATD1 [NCBI] 0.000250944
MVP [NCBI] 0.00021635
sotos syndrome [NCBI] 0.000215312
AOS [NCBI] 0.000194956
APOB [NCBI] 0.000162895
growth hormone insensitivity syndrome [NCBI] 0.000152498
SRS [NCBI] 0.000138218
PCOS1 [NCBI] 0.000133096
deafness, sensorineural, with pituitary dwarfism [NCBI] 0.000120776
toes, relative length of first and second [NCBI] 0.000120776
achard syndrome [NCBI] 0.000120776
fingers, relative length of [NCBI] 0.000120776
telecanthus [NCBI] 9.30507e-05
uric acid nephrolithiasis, susceptibility to [NCBI] 9.30507e-05
PTH [NCBI] 8.90524e-05
MADB [NCBI] 8.26158e-05
ALB [NCBI] 8.25186e-05
LWD [NCBI] 7.89548e-05
FIDD [NCBI] 7.58562e-05
ectopia lentis [NCBI] 7.58562e-05
LEPR [NCBI] 7.34581e-05
macrocephaly/autism syndrome [NCBI] 7.08423e-05
macrocephaly, benign familial [NCBI] 7.08423e-05
TRPS3 [NCBI] 7.08423e-05
GHRL [NCBI] 6.78789e-05
ectopia lentis, isolated [NCBI] 6.68564e-05
autism [NCBI] 6.33805e-05
lipomatosis, familial benign cervical [NCBI] 6.07261e-05
TRPS1 [NCBI] 5.66825e-05
MCPH5 [NCBI] 5.60809e-05
GBD1 [NCBI] 5.60809e-05
LPL [NCBI] 5.52661e-05
carnitine palmitoyltransferase ii deficiency, late-onset [NCBI] 5.23467e-05
osteoporosis, juvenile [NCBI] 5.23467e-05
crouzon syndrome [NCBI] 5.07234e-05
chondrodysplasia punctata, autosomal dominant [NCBI] 5.07234e-05
chromosome 18q deletion syndrome [NCBI] 5.07234e-05
EDM1 [NCBI] 5.07234e-05
AD [NCBI] 5.0667e-05
langer mesomelic dysplasia [NCBI] 4.92289e-05
MCPH1 [NCBI] 4.78448e-05
SPCH1 [NCBI] 4.53516e-05
INS [NCBI] 4.52447e-05
BWS [NCBI] 4.44959e-05
BBS [NCBI] 4.44148e-05
pituitary dwarfism i [NCBI] 4.42206e-05
MTTM [NCBI] 4.31927e-05
acyl-coa dehydrogenase, very long-chain, deficiency of [NCBI] 4.31552e-05
LEP [NCBI] 4.15682e-05
GLC3A [NCBI] 4.11946e-05
CCAL2 [NCBI] 4.11946e-05
TRPS1 [NCBI] 4.11946e-05
RIEG1 [NCBI] 4.11946e-05
MADA [NCBI] 3.94256e-05
diastrophic dysplasia [NCBI] 3.94256e-05
glycogen storage disease v [NCBI] 3.86024e-05
andersen cardiodysrhythmic periodic paralysis [NCBI] 3.86024e-05
RCDP1 [NCBI] 3.63397e-05
VDR [NCBI] 3.59002e-05
FPLD2 [NCBI] 3.37157e-05
WBS [NCBI] 3.32394e-05
glycogen storage disease vii [NCBI] 3.25396e-05
HCH [NCBI] 3.19806e-05
GCPS [NCBI] 3.09152e-05
COH1 [NCBI] 3.04068e-05
nijmegen breakage syndrome [NCBI] 3.04068e-05
MTTY [NCBI] 2.98229e-05
RA [NCBI] 2.8628e-05
NPR2 [NCBI] 2.83239e-05
MTTL2 [NCBI] 2.83239e-05
CYP2R1 [NCBI] 2.83239e-05
ENO3 [NCBI] 2.71301e-05
SCS [NCBI] 2.68219e-05
TNFRSF11B [NCBI] 2.65788e-05
BRRS [NCBI] 2.56595e-05
IGFALS [NCBI] 2.53866e-05
obesity [NCBI] 2.52903e-05
down syndrome [NCBI] 2.52903e-05
AN2 [NCBI] 2.49296e-05
WS1 [NCBI] 2.45771e-05
MTTE [NCBI] 2.45479e-05
UCP1 [NCBI] 2.40718e-05
ED1 [NCBI] 2.38954e-05
PHKA1 [NCBI] 2.38897e-05
MTTI [NCBI] 2.32979e-05
HK2 [NCBI] 2.32979e-05
ASPM [NCBI] 2.27605e-05
phosphoglycerate mutase, muscle, deficiency of [NCBI] 2.27605e-05
VEGF [NCBI] 2.21272e-05
SVAS [NCBI] 2.11594e-05
gaucher disease, type i [NCBI] 2.11594e-05
ornithine transcarbamylase deficiency, hyperammonemia due to [NCBI] 2.08845e-05
SGCA [NCBI] 2.06326e-05
CYP1A2 [NCBI] 2.06326e-05
COMP [NCBI] 1.99077e-05
hypogonadotropic hypogonadism [NCBI] 1.98345e-05
AVSD [NCBI] 1.95837e-05
PSACH [NCBI] 1.90952e-05
alopecia, androgenetic [NCBI] 1.88572e-05
GHRHR [NCBI] 1.8812e-05
MDD [NCBI] 1.85047e-05
breast cancer [NCBI] 1.83932e-05
LDHA [NCBI] 1.83136e-05
CCD [NCBI] 1.8167e-05
AHO [NCBI] 1.79445e-05
NS1 [NCBI] 1.75102e-05
RBP4 [NCBI] 1.68475e-05
MTTK [NCBI] 1.61529e-05
PTHR1 [NCBI] 1.58351e-05
MTCO1 [NCBI] 1.56827e-05
CD [NCBI] 1.56108e-05
SHOX [NCBI] 1.55343e-05
ADIPOQ [NCBI] 1.48461e-05
MTCYB [NCBI] 1.48461e-05
CDLS1 [NCBI] 1.44772e-05
MTND1 [NCBI] 1.37878e-05
IGF1 [NCBI] 1.2992e-05
PGK1 [NCBI] 1.2992e-05
MTND4 [NCBI] 1.29003e-05
CMH [NCBI] 1.27569e-05
GCCR [NCBI] 1.23799e-05
PAX3 [NCBI] 1.21374e-05
TG [NCBI] 1.14924e-05
MTTL1 [NCBI] 1.14696e-05
GH1 [NCBI] 1.0124e-05
LMNA [NCBI] 1.00704e-05
SCD [NCBI] 1.00174e-05
FBN1 [NCBI] 9.51543e-06
COL1A1 [NCBI] 9.32783e-06
ACP5 [NCBI] 9.17226e-06
EIG [NCBI] 9.10551e-06
AGER [NCBI] 8.07469e-06
COMT [NCBI] 7.97093e-06
IL6 [NCBI] 7.73123e-06
CASR [NCBI] 7.6329e-06
PLTP [NCBI] 7.53659e-06
PRL [NCBI] 7.37784e-06
APOE [NCBI] 7.0284e-06
fragile x mental retardation syndrome [NCBI] 6.79599e-06
SST [NCBI] 6.56694e-06
FGFR3 [NCBI] 5.16051e-06
PPARA [NCBI] 5.07939e-06
NF1 [NCBI] 5.05212e-06
PD [NCBI] 4.697e-06
PI [NCBI] 4.67882e-06
CPI [NCBI] 4.67863e-06
BCHE [NCBI] 4.36887e-06
SLC6A4 [NCBI] 4.04245e-06
LCAT [NCBI] 4.00202e-06
TPO [NCBI] 3.70702e-06
TH [NCBI] 3.29821e-06
AVP [NCBI] 3.24806e-06
MB [NCBI] 2.77858e-06
ACE [NCBI] 2.56107e-06
RTT [NCBI] 2.44774e-06
PYY [NCBI] 1.94906e-06
RP [NCBI] 1.94896e-06
AR [NCBI] 1.92303e-06
CEACAM5 [NCBI] 1.91001e-06
HD [NCBI] 1.48076e-06
NPY [NCBI] 1.15854e-06
FA [NCBI] 1.06408e-06
CNTF [NCBI] 9.80405e-07
RNASE3 [NCBI] 9.58268e-07
MPO [NCBI] 9.39785e-07
TF [NCBI] 8.53063e-07
AS [NCBI] 5.85639e-07
KLK3 [NCBI] 1.63211e-07
TNF [NCBI] 1.35627e-07
EPO [NCBI] 4.1812e-08
CCK [NCBI] 1.89015e-08
TS [NCBI] 1.55085e-09
CRH [NCBI] 4.0482e-10



Database Center for Life Science