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01 Body Height [NCBI]

Gene


 Gene Link Information
Gain		 01
AIS [NCBI] 0.000368773
STQTL2 [NCBI] 0.000296992
SHOX [NCBI] 0.00015858
STQTL7 [NCBI] 0.0001481
STQTL4 [NCBI] 0.0001481
STQTL3 [NCBI] 0.0001481
STQTL8 [NCBI] 0.0001481
STQTL5 [NCBI] 0.0001481
MHAC [NCBI] 0.0001481
BMND3 [NCBI] 0.0001481
TRNL1 [NCBI] 0.000146402
DBQD [NCBI] 0.000122826
VUR [NCBI] 8.98888e-05
HPT [NCBI] 8.88688e-05
RMRP [NCBI] 7.77653e-05
KCNQ1OT1 [NCBI] 6.00969e-05
IGF1 [NCBI] 5.78922e-05
AIR [NCBI] 4.98327e-05
GHR [NCBI] 4.91946e-05
PTH [NCBI] 3.28168e-05
VDR [NCBI] 3.20727e-05
IGFBP3 [NCBI] 3.02761e-05
GHRL [NCBI] 2.27981e-05
LEP [NCBI] 2.2381e-05
FGFR3 [NCBI] 2.2006e-05
GER [NCBI] 1.82235e-05
GH1 [NCBI] 1.72956e-05
GHRH [NCBI] 1.578e-05
STAT5B [NCBI] 1.34786e-05
ZBTB38 [NCBI] 1.3089e-05
TRH [NCBI] 1.21979e-05
GPR126 [NCBI] 1.21935e-05
CST3 [NCBI] 1.15981e-05
ESR1 [NCBI] 1.07756e-05
PRL [NCBI] 1.06062e-05
GHSR [NCBI] 9.53128e-06
POU1F1 [NCBI] 8.89554e-06
IGFALS [NCBI] 8.06053e-06
CYP21A2 [NCBI] 7.60426e-06
HHIP [NCBI] 7.58321e-06
ATP8B1 [NCBI] 7.06813e-06
PPARG [NCBI] 6.52965e-06
HMGA2 [NCBI] 6.38481e-06
PTPN11 [NCBI] 6.29427e-06
CFTR [NCBI] 6.20443e-06
IGF2 [NCBI] 5.96969e-06
PTH1R [NCBI] 5.90636e-06
ADIPOQ [NCBI] 5.50769e-06
MRAP [NCBI] 5.39409e-06
INS [NCBI] 5.31855e-06
MC4R [NCBI] 5.06399e-06
IL6 [NCBI] 4.94789e-06
LEPR [NCBI] 4.76595e-06
CASR [NCBI] 4.72754e-06
GHRHR [NCBI] 4.43967e-06
COL1A1 [NCBI] 4.42851e-06
TRAPPC2 [NCBI] 4.41726e-06
IHH [NCBI] 4.31284e-06
BAT1 [NCBI] 4.29333e-06
SRY [NCBI] 4.14574e-06
CSH1 [NCBI] 4.11839e-06
HESX1 [NCBI] 4.10262e-06
AHSG [NCBI] 3.98553e-06
NSD1 [NCBI] 3.98553e-06
TNF [NCBI] 3.92014e-06
MTPN [NCBI] 3.6278e-06
KAL1 [NCBI] 3.58283e-06
GDF5 [NCBI] 3.55689e-06
IL2RG [NCBI] 3.42997e-06
DNASE1 [NCBI] 3.30587e-06
SHBG [NCBI] 3.23689e-06
FBN1 [NCBI] 3.18001e-06
ZNF782 [NCBI] 3.16744e-06
IL12B [NCBI] 3.10502e-06
FMR1 [NCBI] 3.08398e-06
TF [NCBI] 3.07634e-06
ZNF510 [NCBI] 2.89798e-06
RTP3 [NCBI] 2.89798e-06
RTP4 [NCBI] 2.89798e-06
IQCH [NCBI] 2.89798e-06
DLEU7 [NCBI] 2.89798e-06
RTP2 [NCBI] 2.89798e-06
IGFBP1 [NCBI] 2.84821e-06
REEP3 [NCBI] 2.80642e-06
REEP6 [NCBI] 2.80642e-06
LCORL [NCBI] 2.80642e-06
RTP1 [NCBI] 2.80642e-06
C7orf10 [NCBI] 2.73029e-06
REEP4 [NCBI] 2.73029e-06
RETN [NCBI] 2.71314e-06
IGF1R [NCBI] 2.66819e-06
ADAMTSL3 [NCBI] 2.66512e-06
ACTL7A [NCBI] 2.66512e-06
CYP19A1 [NCBI] 2.63443e-06
C7orf11 [NCBI] 2.60816e-06
REEP2 [NCBI] 2.55756e-06
PRSS7 [NCBI] 2.55756e-06
BARX1 [NCBI] 2.51205e-06
MATN1 [NCBI] 2.49301e-06
AR [NCBI] 2.49263e-06
REEP5 [NCBI] 2.47069e-06
UQCC [NCBI] 2.47069e-06
REEP1 [NCBI] 2.43279e-06
OSCAR [NCBI] 2.43279e-06
CRP [NCBI] 2.37369e-06
TPO [NCBI] 2.32812e-06
EVC [NCBI] 2.30666e-06
JAK2 [NCBI] 2.30021e-06
PLXNA2 [NCBI] 2.25471e-06
TRIP11 [NCBI] 2.23082e-06
ADRB2 [NCBI] 2.21357e-06
ATP2B3 [NCBI] 2.20812e-06
SMARCAL1 [NCBI] 2.14616e-06
LHX3 [NCBI] 2.10911e-06
TBCE [NCBI] 2.10911e-06
HOMER1 [NCBI] 2.07488e-06
JAZF1 [NCBI] 2.05869e-06
OPHN1 [NCBI] 2.05869e-06
TAS2R38 [NCBI] 2.05869e-06
BBS1 [NCBI] 1.99918e-06
PROP1 [NCBI] 1.99918e-06
CLCN7 [NCBI] 1.93438e-06
ONECUT1 [NCBI] 1.93438e-06
SRD5A1 [NCBI] 1.93438e-06
TRPS1 [NCBI] 1.91086e-06
EFEMP1 [NCBI] 1.89955e-06
CLCN5 [NCBI] 1.88851e-06
ATP2B1 [NCBI] 1.85694e-06
EXT1 [NCBI] 1.84689e-06
EXT2 [NCBI] 1.84689e-06
BGLAP [NCBI] 1.83706e-06
PITX2 [NCBI] 1.81803e-06
GNA12 [NCBI] 1.80881e-06
MCPH1 [NCBI] 1.79977e-06
GAD2 [NCBI] 1.78222e-06
NPHP1 [NCBI] 1.78222e-06
ASPM [NCBI] 1.7737e-06
ACAN [NCBI] 1.74115e-06
LIPE [NCBI] 1.70352e-06
LCT [NCBI] 1.69636e-06
CHRNA4 [NCBI] 1.67555e-06
TG [NCBI] 1.67044e-06
PAPPA [NCBI] 1.66882e-06
GLB1 [NCBI] 1.66882e-06
NAMPT [NCBI] 1.63046e-06
CTSK [NCBI] 1.62437e-06
NR0B1 [NCBI] 1.61837e-06
ABCG8 [NCBI] 1.6066e-06
CEACAM1 [NCBI] 1.59513e-06
FTO [NCBI] 1.59513e-06
ABCG5 [NCBI] 1.59513e-06
PTCH1 [NCBI] 1.59513e-06
MTTP [NCBI] 1.58395e-06
FOXC1 [NCBI] 1.5677e-06
APOB [NCBI] 1.55714e-06
IGF2R [NCBI] 1.53686e-06
ATRX [NCBI] 1.52222e-06
HRG [NCBI] 1.50804e-06
EPO [NCBI] 1.50747e-06
SLC12A3 [NCBI] 1.50341e-06
SOS1 [NCBI] 1.4943e-06
IRS1 [NCBI] 1.4918e-06
GAA [NCBI] 1.44729e-06
PHEX [NCBI] 1.44729e-06
EDA [NCBI] 1.44325e-06
SOX10 [NCBI] 1.43529e-06
THRB [NCBI] 1.42361e-06
FSHR [NCBI] 1.41599e-06
IL5 [NCBI] 1.41223e-06
NCOA3 [NCBI] 1.40851e-06
HSD11B1 [NCBI] 1.40851e-06
FABP2 [NCBI] 1.3763e-06
BMP6 [NCBI] 1.36607e-06
POLG [NCBI] 1.36272e-06
CHI3L1 [NCBI] 1.35608e-06
PDGFRA [NCBI] 1.35608e-06
TGM2 [NCBI] 1.30047e-06
KCNJ11 [NCBI] 1.29186e-06
DAZ1 [NCBI] 1.27512e-06
COL1A2 [NCBI] 1.25638e-06
MTHFR [NCBI] 1.24798e-06
UBE3A [NCBI] 1.24602e-06
TCF7L2 [NCBI] 1.2359e-06
PTPRN [NCBI] 1.23093e-06
CD99 [NCBI] 1.21875e-06
LCN2 [NCBI] 1.20225e-06
COMP [NCBI] 1.19537e-06
PARK7 [NCBI] 1.1886e-06
INSL3 [NCBI] 1.18414e-06
ADRB3 [NCBI] 1.18193e-06
ENPP1 [NCBI] 1.17536e-06
CYP27A1 [NCBI] 1.13006e-06
AMH [NCBI] 1.11282e-06
COL2A1 [NCBI] 1.10723e-06
ATXN3 [NCBI] 1.10723e-06
RUNX2 [NCBI] 1.09807e-06
AQP2 [NCBI] 1.05502e-06
CDK6 [NCBI] 1.02961e-06
GNAS [NCBI] 1.02654e-06
MLX [NCBI] 9.87146e-07
LMNA [NCBI] 9.6943e-07
MEFV [NCBI] 9.65447e-07
LPL [NCBI] 9.60072e-07
HNF4A [NCBI] 9.563e-07
CS [NCBI] 9.28805e-07
CYBA [NCBI] 9.23997e-07
PIH [NCBI] 8.61015e-07
GDNF [NCBI] 8.43983e-07
CYBB [NCBI] 8.40078e-07
IL1A [NCBI] 8.33335e-07
PRNP [NCBI] 8.31429e-07
MECP2 [NCBI] 7.89939e-07
HNF1B [NCBI] 7.773e-07
ALB [NCBI] 7.33426e-07
HNF1A [NCBI] 7.26816e-07
ATM [NCBI] 7.19603e-07
NOG [NCBI] 7.001e-07
SHC1 [NCBI] 6.99421e-07
UCP3 [NCBI] 6.88728e-07
SLC2A4 [NCBI] 6.86757e-07
PON1 [NCBI] 6.67587e-07
SERPINE1 [NCBI] 6.44051e-07
F2 [NCBI] 6.38825e-07
F5 [NCBI] 6.27471e-07
NOD2 [NCBI] 6.25242e-07
APOE [NCBI] 6.23116e-07
HLA-A [NCBI] 6.20275e-07
CNTF [NCBI] 6.13218e-07
IFNGR1 [NCBI] 5.95898e-07
TNFRSF11A [NCBI] 5.91315e-07
GJB2 [NCBI] 5.77908e-07
TNFRSF11B [NCBI] 5.59857e-07
MS [NCBI] 5.5799e-07
CCL2 [NCBI] 5.53888e-07
HLA-B [NCBI] 5.42248e-07
NPY [NCBI] 5.26504e-07
CETP [NCBI] 5.03562e-07
COMT [NCBI] 4.90453e-07
HLA-DRB1 [NCBI] 3.82593e-07
BMP2 [NCBI] 3.70746e-07
AFP [NCBI] 2.68212e-07
CAT [NCBI] 2.54671e-07
HGF [NCBI] 2.01435e-07
MPO [NCBI] 1.9883e-07
VIP [NCBI] 1.7032e-07
TGFB1 [NCBI] 1.54806e-07
BDNF [NCBI] 1.36396e-07
CCK [NCBI] 1.34847e-07
CDKN1A [NCBI] 3.63379e-08



OMIM


 OMIM Link Information
gain		 01
stature quantitative trait locus 3 [NCBI] 0.00333131
stature quantitative trait locus 6 [NCBI] 0.00333131
SRS [NCBI] 0.00332714
GCY [NCBI] 0.00299584
pygmy [NCBI] 0.00273348
stature as a quantitative trait [NCBI] 0.00260552
stature quantitative trait locus 8 [NCBI] 0.00249555
stature quantitative trait locus 5 [NCBI] 0.00249555
stature quantitative trait locus 2 [NCBI] 0.00249555
kbg syndrome [NCBI] 0.00206767
spondyloepimetaphyseal dysplasia, sponastrime type [NCBI] 0.00185667
acromicric dysplasia [NCBI] 0.00166176
hypertension with brachydactyly [NCBI] 0.0014143
dubowitz syndrome [NCBI] 0.00137944
spondylometaphyseal dysplasia, kozlowski type [NCBI] 0.00129892
apnea, obstructive sleep [NCBI] 0.00123351
costovertebral segmentation anomalies [NCBI] 0.00113628
RA [NCBI] 0.00106342
precocious puberty [NCBI] 0.00094103
PWS [NCBI] 0.000933137
DA4 [NCBI] 0.000829916
stature quantitative trait locus 7 [NCBI] 0.000829916
methionine malabsorption syndrome [NCBI] 0.000829916
vertebral hypoplasia with lumbar kyphosis [NCBI] 0.000829916
stature quantitative trait locus 4 [NCBI] 0.000829916
deafness, congenital, with vitiligo and achalasia [NCBI] 0.000829916
ear, patella, short stature syndrome [NCBI] 0.000815972
SLE [NCBI] 0.000791186
ISS [NCBI] 0.000734348
CF [NCBI] 0.000630866
OD [NCBI] 0.000621273
LWD [NCBI] 0.00061806
ocular hypotelorism, submucosal cleft palate, and hypospadias [NCBI] 0.000567203
spondyloepiphyseal dysplasia tarda, autosomal recessive [NCBI] 0.000567203
SHOX [NCBI] 0.000530467
NS1 [NCBI] 0.000496143
GH1 [NCBI] 0.000482054
hairy elbows [NCBI] 0.000469601
adducted thumb-clubfoot syndrome [NCBI] 0.000469601
megalencephaly [NCBI] 0.000469601
kenny-caffey syndrome, type 2 [NCBI] 0.000469601
WTS [NCBI] 0.000469601
MHAC [NCBI] 0.000469601
porokeratosis of mibelli [NCBI] 0.000407097
cholestasis-lymphedema syndrome [NCBI] 0.000407097
eosinophilia, familial [NCBI] 0.000407097
pituitary dwarfism i [NCBI] 0.000382572
gapo syndrome [NCBI] 0.000361262
spondyloepiphyseal dysplasia tarda, autosomal dominant [NCBI] 0.000361262
kyphomelic dysplasia [NCBI] 0.000325244
spondyloepimetaphyseal dysplasia with multiple dislocations [NCBI] 0.000325244
GHR [NCBI] 0.000314321
short stature, idiopathic, autosomal [NCBI] 0.000311506
short syndrome [NCBI] 0.000296308
BMND3 [NCBI] 0.000295714
DA5 [NCBI] 0.000295714
DBQD [NCBI] 0.000295714
acrodysostosis [NCBI] 0.000295714
gordon syndrome [NCBI] 0.000270795
IGES [NCBI] 0.000249323
mohr syndrome [NCBI] 0.000249323
hunter-mcalpine craniosynostosis syndrome [NCBI] 0.000237944
growth-mental deficiency syndrome of myhre [NCBI] 0.000237944
spatial visualization, aptitude for [NCBI] 0.000230528
CD [NCBI] 0.000215692
acroosteolysis with osteoporosis and changes in skull and mandible [NCBI] 0.000213871
growth hormone insensitivity syndrome [NCBI] 0.000213749
hypophosphatemic rickets, x-linked dominant [NCBI] 0.000211162
acromesomelic dysplasia, hunter-thompson type [NCBI] 0.000209839
alopecia-contractures-dwarfism mental retardation syndrome [NCBI] 0.000203364
devriendt syndrome [NCBI] 0.000203364
ACH [NCBI] 0.000202147
microcephaly, autosomal dominant [NCBI] 0.000198961
marden-walker syndrome [NCBI] 0.000198961
AD [NCBI] 0.000197482
MAS [NCBI] 0.000185922
IGFALS [NCBI] 0.000171552
CHH [NCBI] 0.000167614
pituitary dwarfism due to isolated growth hormone deficiency, autosomal dominant [NCBI] 0.000165666
HCH [NCBI] 0.000163918
twinning, dizygotic [NCBI] 0.000162113
VDR [NCBI] 0.000156915
martsolf syndrome [NCBI] 0.000148066
branchial arch syndrome, x-linked [NCBI] 0.000148066
marshall-smith syndrome [NCBI] 0.000148066
insulin-like growth factor i deficiency [NCBI] 0.000136322
trismus-pseudocamptodactyly syndrome [NCBI] 0.000136322
TRPS3 [NCBI] 0.000136322
TRPS1 [NCBI] 0.000134816
faciogenital dysplasia [NCBI] 0.000131929
MRXHF1 [NCBI] 0.000124083
floating-harbor syndrome [NCBI] 0.000120087
three m syndrome [NCBI] 0.000120087
JBTS1 [NCBI] 0.000117958
PTH [NCBI] 0.000114041
MVP [NCBI] 0.000104294
IS1 [NCBI] 0.000103143
AHO [NCBI] 0.000102903
thumb deformity and alopecia [NCBI] 0.00010166
gonadal dysgenesis, xy type, with associated anomalies [NCBI] 0.00010166
spondylometaphyseal dysplasia, algerian type [NCBI] 0.00010166
patent ductus arteriosus and bicuspid aortic valve with hand anomalies [NCBI] 0.00010166
phenformin 4-hydroxylation [NCBI] 0.00010166
mastocytosis, cutaneous, with short stature, conductive hearing loss and microtia [NCBI] 0.00010166
disproportionate short stature with ptosis and valvular heart lesions [NCBI] 0.00010166
cleidorhizomelic syndrome [NCBI] 0.00010166
microcephaly with cervical spine fusion anomalies [NCBI] 0.00010166
hand and foot deformity with flat facies [NCBI] 0.00010166
corneodermatoosseous syndrome [NCBI] 0.00010166
pituitary dwarfism with small sella turcica [NCBI] 0.00010166
metaphyseal anadysplasia [NCBI] 0.00010166
arthrogryposis, distal, type 2e [NCBI] 0.00010166
rhizomelic dysplasia, patterson-lowry type [NCBI] 0.00010166
arthrogryposis, distal, with peculiar facies and hydronephrosis [NCBI] 0.00010166
edema, familial idiopathic, prepubertal [NCBI] 0.00010166
laryngotracheal stenosis, progressive, with short stature and arthropathy [NCBI] 0.00010166
brachydactyly-distal symphalangism syndrome [NCBI] 0.00010166
asthma, short stature, and elevated iga [NCBI] 0.00010166
short stature syndrome, brussels type [NCBI] 0.00010166
ulnar/fibular ray defect and brachydactyly [NCBI] 0.00010166
KPC [NCBI] 0.00010166
marfanoid mental retardation syndrome, autosomal [NCBI] 0.00010166
BDA1 [NCBI] 0.0001
SEDT [NCBI] 9.62949e-05
GHRH [NCBI] 9.47278e-05
multiple pterygium syndrome, escobar variant [NCBI] 9.29249e-05
sotos syndrome [NCBI] 8.95462e-05
adrenal hyperplasia, congenital, due to 21-hydroxylase deficiency [NCBI] 8.49479e-05
PFIC1 [NCBI] 8.4343e-05
osteogenesis imperfecta, type iv [NCBI] 7.74044e-05
IGF1 [NCBI] 7.45007e-05
aarskog syndrome [NCBI] 7.40114e-05
cleft lip/palate with abnormal thumbs and microcephaly [NCBI] 7.40114e-05
acrofrontofacionasal dysostosis, severe [NCBI] 7.40114e-05
STQTL9 [NCBI] 7.40114e-05
bowing of legs, anterior, with dwarfism [NCBI] 7.40114e-05
radial-renal syndrome [NCBI] 7.40114e-05
sjogren-larsson-like ichthyosis without cns or eye involvement [NCBI] 7.40114e-05
body length, mouse, human homolog [NCBI] 7.40114e-05
nicolaides-baraitser syndrome [NCBI] 7.40114e-05
creases, infra-auricular cutaneous, with tall stature and advanced bone age [NCBI] 7.40114e-05
TCC [NCBI] 7.40114e-05
prader-willi habitus, osteopenia, and camptodactyly [NCBI] 7.40114e-05
osteogenesis imperfecta, type iii [NCBI] 7.34294e-05
bartter syndrome, type 3 [NCBI] 6.98582e-05
PSACH [NCBI] 6.53758e-05
ALMS [NCBI] 6.5109e-05
RCDP1 [NCBI] 6.3662e-05
craniofacial dysostosis with diaphyseal hyperplasia [NCBI] 6.36539e-05
camera-marugo-cohen syndrome [NCBI] 6.36539e-05
NS4 [NCBI] 6.36539e-05
macrocephaly [NCBI] 6.36539e-05
osteogenesis imperfecta, type i [NCBI] 6.31746e-05
TTDN1 [NCBI] 6.11373e-05
PTHR1 [NCBI] 5.95262e-05
OPTB2 [NCBI] 5.69718e-05
ruvalcaba syndrome [NCBI] 5.69718e-05
varicose veins [NCBI] 5.69718e-05
precocious puberty, male-limited [NCBI] 5.69718e-05
nevo syndrome [NCBI] 5.69718e-05
ectopia lentis [NCBI] 5.69718e-05
kabuki syndrome [NCBI] 5.28655e-05
enterokinase deficiency [NCBI] 5.20352e-05
ODG1 [NCBI] 5.20352e-05
iris coloboma with ptosis, hypertelorism, and mental retardation [NCBI] 5.20352e-05
TTDN1 [NCBI] 5.20352e-05
GCS1 [NCBI] 5.20352e-05
renal tubular acidosis, proximal, with ocular abnormalities and mental retardation [NCBI] 5.20352e-05
COH1 [NCBI] 5.18715e-05
CDLS1 [NCBI] 5.08523e-05
BTHS [NCBI] 4.99553e-05
thyrotropin deficiency, isolated [NCBI] 4.81267e-05
buschke-ollendorff syndrome [NCBI] 4.81267e-05
BDE [NCBI] 4.81267e-05
ectopia lentis, isolated [NCBI] 4.81267e-05
serpentine fibula-polycystic kidney syndrome [NCBI] 4.81267e-05
PPNAD1 [NCBI] 4.81267e-05
TRAPPC2 [NCBI] 4.70565e-05
IGFBP3 [NCBI] 4.53638e-05
AEXS [NCBI] 4.48976e-05
osteogenesis imperfecta, type iia [NCBI] 4.33015e-05
proteinuria, low molecular weight, with hypercalciuria and nephrocalcinosis [NCBI] 4.21513e-05
TRS [NCBI] 4.21513e-05
PHA2 [NCBI] 4.21513e-05
ODG2 [NCBI] 4.21513e-05
AMDM [NCBI] 4.21513e-05
sickle cell anemia [NCBI] 4.18467e-05
C7ORF10 [NCBI] 4.05578e-05
NF1 [NCBI] 4.01365e-05
EDM4 [NCBI] 3.9766e-05
growth hormone insensitivity with immunodeficiency [NCBI] 3.9766e-05
DA1 [NCBI] 3.76609e-05
WZS [NCBI] 3.76609e-05
PBT [NCBI] 3.76609e-05
hyperostosis corticalis generalisata [NCBI] 3.76609e-05
spondyloepimetaphyseal dysplasia, strudwick type [NCBI] 3.76609e-05
SMMCI [NCBI] 3.76609e-05
GNRH1 [NCBI] 3.69408e-05
IGF1R [NCBI] 3.64515e-05
HOS [NCBI] 3.60886e-05
BDB1 [NCBI] 3.57797e-05
BDC [NCBI] 3.57797e-05
WSS [NCBI] 3.57797e-05
OSMED [NCBI] 3.57797e-05
IFD [NCBI] 3.57797e-05
STAT5B [NCBI] 3.50756e-05
GHRL [NCBI] 3.50756e-05
DA2B [NCBI] 3.40815e-05
HHS [NCBI] 3.40815e-05
osteoporosis, juvenile [NCBI] 3.40815e-05
methylmalonic aciduria and homocystinuria, cblc type [NCBI] 3.40815e-05
corticosterone methyloxidase type ii deficiency [NCBI] 3.40815e-05
glutathione synthetase deficiency [NCBI] 3.40815e-05
TD1 [NCBI] 3.38724e-05
chondrodysplasia punctata, autosomal dominant [NCBI] 3.25356e-05
adrenal hyperplasia, congenital, due to steroid 11-beta-hydroxylase deficiency [NCBI] 3.25356e-05
cutis laxa, autosomal recessive, type ii [NCBI] 3.25356e-05
SHOXY [NCBI] 3.23167e-05
ATRX [NCBI] 3.19737e-05
RP [NCBI] 3.1187e-05
GCCD1 [NCBI] 3.11185e-05
NFNS [NCBI] 3.11185e-05
UMS [NCBI] 2.98119e-05
propionic acidemia [NCBI] 2.98119e-05
MCPH1 [NCBI] 2.98119e-05
hypophosphatasia, adult type [NCBI] 2.98119e-05
SOST [NCBI] 2.98119e-05
AIS [NCBI] 2.88844e-05
PPAC [NCBI] 2.86009e-05
ehlers-danlos syndrome, type vi [NCBI] 2.86009e-05
CSID [NCBI] 2.86009e-05
hartnup disorder [NCBI] 2.86009e-05
phenylketonuria [NCBI] 2.80239e-05
OPTB3 [NCBI] 2.74735e-05
pituitary dwarfism iii [NCBI] 2.74735e-05
MC4R [NCBI] 2.69025e-05
BGS [NCBI] 2.642e-05
FBS [NCBI] 2.642e-05
leopard syndrome 1 [NCBI] 2.642e-05
weaver syndrome [NCBI] 2.642e-05
FGFR3 [NCBI] 2.57064e-05
PRSS7 [NCBI] 2.56983e-05
PLXNA2 [NCBI] 2.56983e-05
SHOX2 [NCBI] 2.56983e-05
frank-ter haar syndrome [NCBI] 2.56983e-05
NPR2 [NCBI] 2.56983e-05
ESX1L [NCBI] 2.56983e-05
BFLS [NCBI] 2.5432e-05
MYH8 [NCBI] 2.45069e-05
DA2A [NCBI] 2.45027e-05
masa syndrome [NCBI] 2.45027e-05
CDPX1 [NCBI] 2.36261e-05
histidinemia [NCBI] 2.36261e-05
SRY [NCBI] 2.28919e-05
mucolipidosis iv [NCBI] 2.27974e-05
SRD5A1 [NCBI] 2.26709e-05
CHNG2 [NCBI] 2.2012e-05
glycogen storage disease iii [NCBI] 2.2012e-05
diastrophic dysplasia [NCBI] 2.2012e-05
FBN1 [NCBI] 2.18643e-05
COL1A1 [NCBI] 2.14799e-05
TRPS1 [NCBI] 2.12758e-05
ATP8B1 [NCBI] 2.12758e-05
SHC1 [NCBI] 2.12758e-05
SOS1 [NCBI] 2.12758e-05
SCDO1 [NCBI] 2.12663e-05
osteoporosis [NCBI] 2.12663e-05
FGD1 [NCBI] 2.06864e-05
NPPB [NCBI] 2.06864e-05
OCRL [NCBI] 2.05569e-05
AHC [NCBI] 2.05569e-05
TBX3 [NCBI] 2.01513e-05
diabetes insipidus, nephrogenic, x-linked [NCBI] 1.9881e-05
OKS [NCBI] 1.92358e-05
BGLAP [NCBI] 1.89053e-05
PRL [NCBI] 1.83584e-05
LEP [NCBI] 1.81291e-05
COL5A1 [NCBI] 1.8035e-05
hypophosphatasia, infantile [NCBI] 1.74639e-05
PAPPA [NCBI] 1.73672e-05
GAD2 [NCBI] 1.67693e-05
TBX5 [NCBI] 1.64924e-05
SGBS1 [NCBI] 1.64009e-05
PLOD1 [NCBI] 1.62284e-05
GHSR [NCBI] 1.62284e-05
EBP [NCBI] 1.62284e-05
LHB [NCBI] 1.57347e-05
CYP11B1 [NCBI] 1.57347e-05
CTSK [NCBI] 1.50669e-05
SJS1 [NCBI] 1.49551e-05
CDPX2 [NCBI] 1.49551e-05
TNF [NCBI] 1.48941e-05
PROP1 [NCBI] 1.48609e-05
HMGA2 [NCBI] 1.46622e-05
FABP2 [NCBI] 1.46622e-05
SMA3 [NCBI] 1.45083e-05
FIH [NCBI] 1.45083e-05
CYP11B2 [NCBI] 1.42849e-05
KCNJ11 [NCBI] 1.42849e-05
PTPN11 [NCBI] 1.41055e-05
nijmegen breakage syndrome [NCBI] 1.40773e-05
ACP1 [NCBI] 1.32866e-05
NR0B1 [NCBI] 1.28482e-05
IGER [NCBI] 1.24964e-05
RSTS [NCBI] 1.24964e-05
mucopolysaccharidosis type iva [NCBI] 1.24426e-05
KAL1 [NCBI] 1.20653e-05
porphyria cutanea tarda [NCBI] 1.19452e-05
ABL [NCBI] 1.14417e-05
SCS [NCBI] 1.1112e-05
INSL3 [NCBI] 1.09715e-05
SLC2A2 [NCBI] 1.06832e-05
INS [NCBI] 1.04716e-05
CYP19A1 [NCBI] 1.02356e-05
galactosemia [NCBI] 1.01819e-05
LNS [NCBI] 1.01819e-05
GPT [NCBI] 9.9037e-06
obesity [NCBI] 9.89018e-06
TF [NCBI] 9.5562e-06
FSHR [NCBI] 9.44319e-06
CLS [NCBI] 9.33192e-06
BMP2 [NCBI] 9.08926e-06
ARPKD [NCBI] 9.06474e-06
MTTL1 [NCBI] 9.0214e-06
HRG [NCBI] 8.8884e-06
LCT [NCBI] 8.50977e-06
LEPR [NCBI] 7.88434e-06
SHBG [NCBI] 7.56833e-06
ATM [NCBI] 6.79682e-06
HGPS [NCBI] 6.76631e-06
gaucher disease, type i [NCBI] 6.76631e-06
CCK [NCBI] 6.59771e-06
LPI [NCBI] 6.37654e-06
velocardiofacial syndrome [NCBI] 6.37654e-06
CEACAM5 [NCBI] 6.00096e-06
DMD [NCBI] 5.95056e-06
BDNF [NCBI] 5.91096e-06
NPY [NCBI] 5.90974e-06
CRH [NCBI] 5.75866e-06
asthma, susceptibility to [NCBI] 5.65547e-06
FA [NCBI] 5.54408e-06
VIP [NCBI] 5.53634e-06
CASR [NCBI] 5.37607e-06
IBD1 [NCBI] 5.32189e-06
ABP1 [NCBI] 5.19942e-06
alopecia, androgenetic [NCBI] 5.16139e-06
SDS [NCBI] 5.00492e-06
breast cancer [NCBI] 4.85237e-06
IHH [NCBI] 4.63735e-06
OXT [NCBI] 4.53911e-06
CPI [NCBI] 4.45511e-06
COMP [NCBI] 4.10556e-06
CGD [NCBI] 4.0137e-06
MPO [NCBI] 3.84922e-06
HGF [NCBI] 3.62791e-06
AFP [NCBI] 3.42578e-06
FMF [NCBI] 3.09892e-06
AVP [NCBI] 3.03547e-06
AMH [NCBI] 2.95602e-06
APS1 [NCBI] 2.86883e-06
lymphoma, non-hodgkin, familial [NCBI] 2.69771e-06
APOB [NCBI] 2.36324e-06
CAT [NCBI] 2.15811e-06
TPO [NCBI] 1.91494e-06
SCZD [NCBI] 1.8304e-06
TG [NCBI] 1.47743e-06
RTT [NCBI] 1.42258e-06
MFS [NCBI] 1.26429e-06
KLK3 [NCBI] 9.33191e-07
BBS [NCBI] 8.83115e-07
AR [NCBI] 8.20197e-07
CYP1A1 [NCBI] 7.77516e-07
ALB [NCBI] 6.70695e-07
SOD2 [NCBI] 5.13428e-07
ACP5 [NCBI] 4.60236e-07
BWS [NCBI] 4.51373e-07
HD [NCBI] 3.36209e-07
COMT [NCBI] 2.28944e-07
PTHLH [NCBI] 1.87335e-07
EPO [NCBI] 1.32194e-07
CNTF [NCBI] 1.02565e-07
TNFRSF11B [NCBI] 5.44983e-08
LPL [NCBI] 5.12808e-08
HBB [NCBI] 7.74828e-09
PPARA [NCBI] 7.16725e-09
WBS [NCBI] 4.3409e-09
AS [NCBI] 1.40281e-09
fragile x mental retardation syndrome [NCBI] 4.37761e-11



Database Center for Life Science