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MeSH keywords -> Related genes, diseases (OMIM)


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01 Syndactyly [NCBI]

Gene


 Gene Link Information
Gain		 01
SDTY1 [NCBI] 0.000741367
AFA [NCBI] 0.000532523
MSSD [NCBI] 0.000367544
SPD3 [NCBI] 0.000367544
MRSS [NCBI] 0.000367544
CRS [NCBI] 0.000306807
HOXD13 [NCBI] 0.000284504
GLI3 [NCBI] 0.000142038
GJA1 [NCBI] 0.000125845
FREM2 [NCBI] 5.6008e-05
FGFR2 [NCBI] 3.84483e-05
RASSF8 [NCBI] 2.64853e-05
HOXD12 [NCBI] 2.40555e-05
HOXD8 [NCBI] 2.3522e-05
HOXD11 [NCBI] 2.30608e-05
NOG [NCBI] 2.18829e-05
HOXD10 [NCBI] 1.95815e-05
ROR2 [NCBI] 1.92829e-05
HOXA13 [NCBI] 1.80881e-05
SHH [NCBI] 1.7569e-05
FBLN1 [NCBI] 1.73637e-05
DHCR7 [NCBI] 1.69783e-05
TP63 [NCBI] 1.62415e-05
IRF6 [NCBI] 1.57137e-05
FAM58A [NCBI] 1.32335e-05
MBOAT1 [NCBI] 1.32335e-05
STK36 [NCBI] 1.23352e-05
AKTIP [NCBI] 1.17519e-05
FRAS1 [NCBI] 1.13182e-05
NID2 [NCBI] 1.09726e-05
EPHA7 [NCBI] 1.02243e-05
FBN2 [NCBI] 9.70536e-06
HOXD9 [NCBI] 9.70536e-06
KRT3 [NCBI] 9.08612e-06
LMBR1 [NCBI] 9.08612e-06
SSPN [NCBI] 8.55457e-06
SCN2A [NCBI] 8.55457e-06
TCIRG1 [NCBI] 8.48007e-06
SEPN1 [NCBI] 8.48007e-06
TBX5 [NCBI] 8.27431e-06
SOST [NCBI] 8.21089e-06
ZFY [NCBI] 7.8228e-06
GREM1 [NCBI] 7.77392e-06
MYOT [NCBI] 7.77392e-06
T [NCBI] 7.59134e-06
FLNA [NCBI] 7.31251e-06
GLI2 [NCBI] 7.20572e-06
IKZF1 [NCBI] 7.10526e-06
GDF5 [NCBI] 7.07305e-06
CRYAB [NCBI] 6.62682e-06
SCN1A [NCBI] 6.48578e-06
NID1 [NCBI] 5.83846e-06
FGFR1 [NCBI] 5.71997e-06
RBL2 [NCBI] 5.55664e-06
SRY [NCBI] 4.87507e-06
BMP4 [NCBI] 4.62828e-06
MYCN [NCBI] 4.47333e-06
LMNA [NCBI] 4.40751e-06
CKAP4 [NCBI] 4.26556e-06
FGFR3 [NCBI] 3.35884e-06
BMP2 [NCBI] 3.14234e-06
EGFR [NCBI] 4.19088e-07



OMIM


 OMIM Link Information
gain		 01
poland syndrome [NCBI] 0.00987441
cenani syndactylism [NCBI] 0.00390963
syndactyly, type i, with microcephaly and mental retardation [NCBI] 0.00325328
syndactyly, type i [NCBI] 0.00273043
GCPS [NCBI] 0.00163111
laurin-sandrow syndrome [NCBI] 0.0014442
tibia, hypoplasia of, with polydactyly [NCBI] 0.00138553
SPD1 [NCBI] 0.00132055
ODDD [NCBI] 0.00122205
rosselli-gulienetti syndrome [NCBI] 0.00112277
fraser syndrome [NCBI] 0.000779586
synpolydactyly 3 [NCBI] 0.000777045
BDA4 [NCBI] 0.000777045
MSSD [NCBI] 0.000777045
HOXD13 [NCBI] 0.000616983
blepharophimosis with ptosis, syndactyly, and short stature [NCBI] 0.000560203
polysyndactyly, crossed [NCBI] 0.000560203
CRSA [NCBI] 0.000560203
hypertelorism, microtia, facial clefting syndrome [NCBI] 0.000426747
oculodentoosseous dysplasia, recessive [NCBI] 0.000426747
SPD2 [NCBI] 0.000403333
kbg syndrome [NCBI] 0.000388139
PPS [NCBI] 0.000382818
CLPED1 [NCBI] 0.000381725
PPD2 [NCBI] 0.000372497
SHFM1 [NCBI] 0.000364291
OSCS [NCBI] 0.000357599
AOS [NCBI] 0.000343086
syndactyly, type iii [NCBI] 0.000341487
SOST [NCBI] 0.000322556
digeorge syndrome/velocardiofacial syndrome spectrum of malformation 2 [NCBI] 0.000310971
klippel-feil syndrome, autosomal dominant [NCBI] 0.000310971
popliteal pterygium syndrome, lethal type [NCBI] 0.000310971
blepharocheilodontic syndrome [NCBI] 0.000310971
SHFLD1 [NCBI] 0.000248175
LRP4 [NCBI] 0.000239952
mohr syndrome [NCBI] 0.00022519
short rib-polydactyly syndrome, type ii [NCBI] 0.0002057
syndactyly, type iv [NCBI] 0.000201484
arterial occlusive disease, progressive, with hypertension, heart defects, bone fragility, and brachysyndactyly [NCBI] 0.000201484
polysyndactyly with cardiac malformation [NCBI] 0.000201484
scott craniodigital syndrome with mental retardation [NCBI] 0.000201484
syndactyly, type v [NCBI] 0.000201484
apert syndrome [NCBI] 0.000198933
megalencephaly-cutis marmorata telangiectatica congenita [NCBI] 0.000198134
schinzel-giedion midface-retraction syndrome [NCBI] 0.000196987
ACC [NCBI] 0.000196987
PHS [NCBI] 0.000187323
GJA1 [NCBI] 0.000177856
acrofrontofacionasal dysostosis, severe [NCBI] 0.000170561
robinow syndrome, autosomal recessive [NCBI] 0.000160923
eem syndrome [NCBI] 0.000156603
TS [NCBI] 0.000156603
GLI3 [NCBI] 0.000150128
dubowitz syndrome [NCBI] 0.000149215
FGFR2 [NCBI] 0.000141674
NLS [NCBI] 0.000138613
FDH [NCBI] 0.00012504
SLOS [NCBI] 0.000124041
SHH [NCBI] 0.000106487
EEC1 [NCBI] 0.000101175
hallux varus and preaxial polysyndactyly [NCBI] 0.000100696
aurocephalosyndactyly [NCBI] 0.000100696
brachydactyly-syndactyly syndrome [NCBI] 0.000100696
dauwerse-peters syndrome [NCBI] 0.000100696
odontotrichoungual-digital-palmar syndrome [NCBI] 0.000100696
ectodermal dysplasia with mental retardation and syndactyly [NCBI] 0.000100696
syndactyly with renal and anogenital malformations [NCBI] 0.000100696
acrorenal syndrome [NCBI] 0.000100696
ackerman syndrome [NCBI] 0.000100696
radioulnar synostosis, radial ray abnormalities, and severe malformations in the male [NCBI] 0.000100696
polydactyly, postaxial, with dental and vertebral anomalies [NCBI] 0.000100696
symphalangism with multiple anomalies of hands and feet [NCBI] 0.000100696
ROR2 [NCBI] 9.98716e-05
DHCR7 [NCBI] 9.41614e-05
DWS [NCBI] 8.26981e-05
FLNA [NCBI] 8.252e-05
contractural arachnodactyly, congenital [NCBI] 8.252e-05
RASSF8 [NCBI] 7.97709e-05
FBLN1 [NCBI] 7.97709e-05
MBOAT1 [NCBI] 7.97709e-05
mental retardation, x-linked, with short stature [NCBI] 7.97709e-05
pterygium syndrome, multiple, autosomal dominant [NCBI] 7.82562e-05
second metatarsal-metacarpal syndrome [NCBI] 7.82562e-05
acrofrontofacionasal dysostosis syndrome [NCBI] 7.82562e-05
cleft palate, cardiac defect, genital anomalies, and ectrodactyly [NCBI] 7.82562e-05
RBS [NCBI] 7.5631e-05
cree mental retardation syndrome [NCBI] 6.98065e-05
alopecia-contractures-dwarfism mental retardation syndrome [NCBI] 6.98065e-05
polydactyly, postaxial [NCBI] 6.98065e-05
preaxial deficiency, postaxial polydactyly, and hypospadias [NCBI] 6.98065e-05
ankyloblepharon filiforme adnatum and cleft palate [NCBI] 6.98065e-05
split-foot deformity with mandibulofacial dysostosis [NCBI] 6.98065e-05
scalp defects and postaxial polydactyly [NCBI] 6.98065e-05
brachydactyly-ectrodactyly with fibular aplasia or hypoplasia [NCBI] 6.98065e-05
multiple pterygium syndrome, aslan type [NCBI] 6.98065e-05
mental retardation, buenos aires type [NCBI] 6.98065e-05
FGFR1 [NCBI] 6.55916e-05
humerospinal dysostosis [NCBI] 6.43307e-05
IDH3G [NCBI] 6.07951e-05
FREM2 [NCBI] 6.07951e-05
femur-fibula-ulna syndrome [NCBI] 6.02672e-05
scalp-ear-nipple syndrome [NCBI] 6.02672e-05
SLC12A2 [NCBI] 5.74205e-05
hypertelorism with esophageal abnormality and hypospadias [NCBI] 5.72762e-05
cleft lip/palate with abnormal thumbs and microcephaly [NCBI] 5.70355e-05
neuroblastoma stage 4s gene [NCBI] 5.4912e-05
HOXD3 [NCBI] 5.4912e-05
BDE [NCBI] 5.20623e-05
ACY1 [NCBI] 5.12523e-05
PVRL1 [NCBI] 4.85879e-05
LMBR1 [NCBI] 4.74843e-05
JWS [NCBI] 4.66993e-05
HOXA13 [NCBI] 4.64918e-05
IKZF1 [NCBI] 4.55901e-05
kindler syndrome [NCBI] 4.52561e-05
hyperostosis corticalis generalisata [NCBI] 4.52561e-05
CRS1 [NCBI] 4.39361e-05
LADD [NCBI] 4.39361e-05
three m syndrome [NCBI] 4.39361e-05
hand-foot-uterus syndrome [NCBI] 4.27203e-05
MCOPS2 [NCBI] 4.27203e-05
MYBPC3 [NCBI] 4.26343e-05
OPD1 [NCBI] 4.15939e-05
c syndrome [NCBI] 4.15939e-05
feingold syndrome [NCBI] 4.15939e-05
PHOX2B [NCBI] 4.08847e-05
EEC3 [NCBI] 3.95635e-05
heterotopia, periventricular, x-linked dominant [NCBI] 3.95635e-05
FMD [NCBI] 3.86418e-05
BMP2 [NCBI] 3.81111e-05
TWIST1 [NCBI] 3.77166e-05
MNS [NCBI] 3.47293e-05
HSS [NCBI] 3.40568e-05
HNA [NCBI] 3.40568e-05
ACLS [NCBI] 3.27975e-05
OFD1 [NCBI] 3.16382e-05
OKS [NCBI] 3.0565e-05
SCDO1 [NCBI] 2.90922e-05
MCOPS7 [NCBI] 2.90922e-05
charge syndrome [NCBI] 2.69347e-05
SPG3A [NCBI] 2.61573e-05
TRPS2 [NCBI] 2.50679e-05
COH1 [NCBI] 2.50679e-05
SCS [NCBI] 2.43874e-05
HNPP [NCBI] 2.14259e-05
FGFR3 [NCBI] 1.65716e-05
DGS [NCBI] 6.05075e-06
MFS [NCBI] 3.04044e-06
EGFR [NCBI] 6.00187e-08



Database Center for Life Science