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MeSH keywords -> Related genes, diseases (OMIM)


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01 Radius [NCBI]


Gene


Gene Link Information
Gain
01
POM121L1 [NCBI] 0.000466155
RRDX [NCBI] 0.000466155
FOP [NCBI] 0.000233805
PTH [NCBI] 7.43221e-05
SHOX [NCBI] 3.04974e-05
BMP2 [NCBI] 3.02017e-05
MPL [NCBI] 2.86542e-05
HOXA11 [NCBI] 1.90623e-05
VDR [NCBI] 1.79945e-05
RECQL4 [NCBI] 1.18562e-05
ACP5 [NCBI] 9.34205e-06
TWIST1 [NCBI] 9.14021e-06
QPCT [NCBI] 6.96919e-06
TBX4 [NCBI] 6.58883e-06
SALL4 [NCBI] 5.92161e-06
TNFRSF11B [NCBI] 5.89897e-06
SULT1E1 [NCBI] 5.68228e-06
PITX2 [NCBI] 5.06672e-06
SALL1 [NCBI] 5.06672e-06
NPPB [NCBI] 4.78806e-06
LIF [NCBI] 4.43606e-06
L1CAM [NCBI] 4.34672e-06
IRAK1 [NCBI] 4.28207e-06
SPARC [NCBI] 4.28207e-06
MYH9 [NCBI] 4.11893e-06
BMP6 [NCBI] 4.01013e-06
FGFR2 [NCBI] 3.67703e-06
VEGFA [NCBI] 3.67107e-06
TGFB1 [NCBI] 3.5957e-06
MSTN [NCBI] 3.58536e-06
FGFR1 [NCBI] 3.58536e-06
COMP [NCBI] 3.4828e-06
CD99 [NCBI] 3.42431e-06
HAPLN1 [NCBI] 3.40699e-06
MMP1 [NCBI] 3.39845e-06
ADIPOQ [NCBI] 3.28609e-06
LEP [NCBI] 3.12893e-06
BMP4 [NCBI] 2.5349e-06
MS [NCBI] 2.50506e-06
JAK2 [NCBI] 1.83183e-06
TNF [NCBI] 1.23951e-06




OMIM


OMIM Link Information
gain
01
thrombocytopenia-absent radius syndrome [NCBI] 0.0289225
BGS [NCBI] 0.00289763
humeroradial synostosis [NCBI] 0.00220685
radial heads, posterior dislocation of [NCBI] 0.00220685
hemifacial microsomia with radial defects [NCBI] 0.00145678
metaphyseal dysplasia, braun-tinschert type [NCBI] 0.00110106
ventriculomegaly with defects of the radius and kidney [NCBI] 0.00110106
mesomelic dwarfism of hypoplastic tibia and radius type [NCBI] 0.00110106
robinow syndrome, autosomal dominant [NCBI] 0.000849683
ulnar hypoplasia [NCBI] 0.000791708
nievergelt syndrome [NCBI] 0.000791708
radioulnar synostosis [NCBI] 0.000738026
AFD1 [NCBI] 0.000693691
mesomelic dysplasia, kantaputra type [NCBI] 0.000675971
omodysplasia [NCBI] 0.000601389
LWD [NCBI] 0.000598661
ABS [NCBI] 0.000556081
microcephalic osteodysplastic primordial dwarfism, type i [NCBI] 0.000546353
radioulnar synostosis with microcephaly, short stature, scoliosis, and mental retardation [NCBI] 0.000513224
microcephalic osteodysplastic primordial dwarfism, type ii [NCBI] 0.000502829
BMND3 [NCBI] 0.000466912
weyers ulnar ray/oligodactyly syndrome [NCBI] 0.000418017
omodysplasia, generalized form [NCBI] 0.000409934
kyphomelic dysplasia [NCBI] 0.000409934
acroosteolysis with osteoporosis and changes in skull and mandible [NCBI] 0.000409934
osteolysis, hereditary, of carpal bones with nephropathy [NCBI] 0.000386605
PTH [NCBI] 0.000348563
radial aplasia, x-linked [NCBI] 0.000341917
humeroradial synostosis [NCBI] 0.000341917
radioulnar synostosis with amegakaryocytic thrombocytopenia [NCBI] 0.000341917
MLRD [NCBI] 0.000246778
vacterl association with hydrocephalus, x-linked [NCBI] 0.000233982
RTS [NCBI] 0.000227812
MBS [NCBI] 0.00021454
paget disease, juvenile [NCBI] 0.000189404
DRRS [NCBI] 0.00018005
radial ray hypoplasia with choanal atresia [NCBI] 0.000170842
metachondromatosis [NCBI] 0.000170842
ulnar agenesis and endocardial fibroelastosis [NCBI] 0.000170842
lethal short-limb skeletal dysplasia, al gazali type [NCBI] 0.000170842
radial hypoplasia, triphalangeal thumbs, hypospadias, and maxillary diastema [NCBI] 0.000170842
radioulnar synostosis, radial ray abnormalities, and severe malformations in the male [NCBI] 0.000170842
ulna and fibula, hypoplasia of [NCBI] 0.000170842
pronation-supination of the forearm, impairment of [NCBI] 0.000170842
radioulnar synostosis, unilateral, with developmental retardation and hypotonia [NCBI] 0.000170842
micromelic dysplasia, congenital, with dislocation of radius [NCBI] 0.000131633
phocomelia-ectrodactyly, ear malformation, deafness, and sinus arrhythmia [NCBI] 0.000131633
radial-renal syndrome [NCBI] 0.000131633
osteopetrosis and infantile neuroaxonal dystrophy [NCBI] 0.000131633
renal dysplasia-limb defects syndrome [NCBI] 0.000131633
omphalocele, diaphragmatic hernia, and radial ray defects [NCBI] 0.000116876
ivic syndrome [NCBI] 0.000116876
HOS [NCBI] 0.00010834
vacterl association with hydrocephalus [NCBI] 0.000107317
corpus callosum, partial agenesis of, x-linked [NCBI] 0.000107317
rapadilino syndrome [NCBI] 0.000107317
humerospinal dysostosis [NCBI] 0.000107317
HOXA11 [NCBI] 0.000107254
por deficiency [NCBI] 9.45889e-05
cleft lip/palate with abnormal thumbs and microcephaly [NCBI] 9.45889e-05
AOII [NCBI] 9.45889e-05
DBA [NCBI] 8.69819e-05
VDR [NCBI] 8.22112e-05
vater association [NCBI] 7.93498e-05
stuve-wiedemann syndrome [NCBI] 7.65798e-05
EDM1 [NCBI] 7.40685e-05
TWIST1 [NCBI] 7.14626e-05
SYM1 [NCBI] 6.96591e-05
camurati-engelmann disease [NCBI] 6.77016e-05
sacral defect with anterior meningocele [NCBI] 6.41754e-05
radial ray deficiency, x-linked [NCBI] 6.04224e-05
EFE [NCBI] 5.9645e-05
robinow syndrome, autosomal recessive [NCBI] 5.82958e-05
RBS [NCBI] 5.24511e-05
PHS [NCBI] 4.85943e-05
TBS [NCBI] 4.6054e-05
FOP [NCBI] 4.44979e-05
SCS [NCBI] 4.37563e-05
TRPS2 [NCBI] 4.10032e-05
CRMO [NCBI] 4.10032e-05
NPPB [NCBI] 4.09616e-05
FANCB [NCBI] 3.97573e-05
RECQL4 [NCBI] 3.87266e-05
NPS [NCBI] 3.85422e-05
plasmin inhibitor deficiency [NCBI] 3.70254e-05
SALL4 [NCBI] 3.56517e-05
SDS [NCBI] 3.47906e-05
TD1 [NCBI] 3.43031e-05
AHO [NCBI] 3.38262e-05
CES [NCBI] 3.07562e-05
SHOX [NCBI] 2.99376e-05
MAS [NCBI] 2.84424e-05
L1CAM [NCBI] 2.5958e-05
SLC4A1 [NCBI] 2.4385e-05
BBS [NCBI] 2.36209e-05
TNFRSF11B [NCBI] 2.31839e-05
FGFR2 [NCBI] 2.02519e-05
FGFR1 [NCBI] 1.95146e-05
BGLAP [NCBI] 1.79334e-05
IHH [NCBI] 1.61323e-05
COMP [NCBI] 1.52002e-05
WBS [NCBI] 1.17949e-05
FA [NCBI] 9.9644e-06
VEGF [NCBI] 1.65143e-06
CD [NCBI] 3.09995e-07
RA [NCBI] 1.65899e-08
TNF [NCBI] 2.89213e-10




Database Center for Life Science