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01 Ulna [NCBI]

Gene


 Gene Link Information
Gain		 01
TUKLS [NCBI] 0.000510938
FOP [NCBI] 0.000278469
TBX3 [NCBI] 4.70044e-05
BMP2 [NCBI] 2.91965e-05
SHOX [NCBI] 2.55512e-05
PTH [NCBI] 1.38115e-05
HOXA11 [NCBI] 1.28872e-05
COMP [NCBI] 9.38708e-06
CD99 [NCBI] 9.26884e-06
CAPS2 [NCBI] 8.44301e-06
BMP7 [NCBI] 7.70712e-06
TBX4 [NCBI] 7.10016e-06
TBX2 [NCBI] 6.54727e-06
ACP5 [NCBI] 6.4304e-06
EXT2 [NCBI] 6.32999e-06
COL9A2 [NCBI] 6.07308e-06
EXT1 [NCBI] 6.03602e-06
PITX2 [NCBI] 5.57731e-06
SS18 [NCBI] 5.37042e-06
DMP1 [NCBI] 5.26418e-06
MYH9 [NCBI] 4.62804e-06
BMP6 [NCBI] 4.51896e-06
FGF23 [NCBI] 4.17912e-06
FGFR1 [NCBI] 4.09274e-06
HAPLN1 [NCBI] 3.91356e-06
MATN1 [NCBI] 3.46713e-06
TP63 [NCBI] 3.33184e-06
G6PD [NCBI] 2.69494e-06
LIF [NCBI] 2.0374e-06
TGFB1 [NCBI] 1.62218e-06
TNF [NCBI] 4.83915e-07



OMIM


 OMIM Link Information
gain		 01
UMS [NCBI] 0.00159478
POADS [NCBI] 0.00157235
tukel syndrome [NCBI] 0.00131262
robinow syndrome, autosomal dominant [NCBI] 0.00126523
thrombocytopenia-absent radius syndrome [NCBI] 0.00103683
ulnar hypoplasia [NCBI] 0.00100225
humeroradial synostosis [NCBI] 0.00100225
nievergelt syndrome [NCBI] 0.00100225
radioulnar synostosis [NCBI] 0.000996198
mesomelic dysplasia, kantaputra type [NCBI] 0.000885498
klippel-feil syndrome, autosomal recessive [NCBI] 0.000809899
microcephalic osteodysplastic primordial dwarfism, type i [NCBI] 0.000753845
femur, unilateral bifid, with monodactylous ectrodactyly [NCBI] 0.000709304
microcephalic osteodysplastic primordial dwarfism, type ii [NCBI] 0.000709304
LWD [NCBI] 0.000647161
weyers ulnar ray/oligodactyly syndrome [NCBI] 0.000646224
kyphomelic dysplasia [NCBI] 0.000613355
femur-fibula-ulna syndrome [NCBI] 0.000608957
radioulnar synostosis with microcephaly, short stature, scoliosis, and mental retardation [NCBI] 0.000537329
OD [NCBI] 0.00041326
MBS [NCBI] 0.000403691
radioulnar synostosis with amegakaryocytic thrombocytopenia [NCBI] 0.00035791
pena-shokeir syndrome, type i [NCBI] 0.000354442
TBX3 [NCBI] 0.000329455
langer mesomelic dysplasia [NCBI] 0.000249908
fibular aplasia or hypoplasia, femoral bowing and poly-, syn-, and oligodactyly [NCBI] 0.000249908
HFM [NCBI] 0.000225454
HOS [NCBI] 0.000219879
camurati-engelmann disease [NCBI] 0.000191686
ABS [NCBI] 0.000180821
ulnar/fibular ray defect and brachydactyly [NCBI] 0.000178801
metachondromatosis [NCBI] 0.000178801
ulnar hypoplasia with lobster-claw deformity of feet [NCBI] 0.000178801
ulnar agenesis and endocardial fibroelastosis [NCBI] 0.000178801
lethal short-limb skeletal dysplasia, al gazali type [NCBI] 0.000178801
radioulnar synostosis, radial ray abnormalities, and severe malformations in the male [NCBI] 0.000178801
fibuloulnar aplasia or hypoplasia with renal abnormalities [NCBI] 0.000178801
ulna and fibula, hypoplasia of [NCBI] 0.000178801
ulnar hypoplasia with mental retardation [NCBI] 0.000178801
ribbing disease [NCBI] 0.000178801
radioulnar synostosis, unilateral, with developmental retardation and hypotonia [NCBI] 0.000178801
EFE [NCBI] 0.000174613
ulnar ray dysgenesis with postaxial polydactyly and renal cystic dysplasia [NCBI] 0.000139575
chondrodysplasia punctata, tibia-metacarpal type [NCBI] 0.000139575
ulna metaphyseal dysplasia syndrome [NCBI] 0.000139575
TRPS2 [NCBI] 0.000134858
HHS [NCBI] 0.000124801
HOXA11 [NCBI] 0.000116311
vacterl association with hydrocephalus [NCBI] 0.000115225
humerospinal dysostosis [NCBI] 0.000115225
fibular aplasia, tibial campomelia, and oligosyndactyly syndrome [NCBI] 0.000115225
spondyloperipheral dysplasia [NCBI] 0.000108118
MLRD [NCBI] 0.000108118
adult syndrome [NCBI] 0.000102464
BDE [NCBI] 0.000102464
por deficiency [NCBI] 0.000102464
caffey disease [NCBI] 0.000102464
tibial hemimelia [NCBI] 0.000102464
MCDS [NCBI] 0.000102464
EEC3 [NCBI] 9.02613e-05
LMS [NCBI] 9.02613e-05
RNS [NCBI] 9.02613e-05
ulna and fibula, absence of, with severe limb deficiency [NCBI] 8.43712e-05
stuve-wiedemann syndrome [NCBI] 8.43712e-05
KAL2 [NCBI] 8.18432e-05
paget disease, juvenile [NCBI] 8.18432e-05
SYM1 [NCBI] 7.74003e-05
COFS1 [NCBI] 7.74003e-05
AFD1 [NCBI] 6.87265e-05
HCH [NCBI] 6.72859e-05
robinow syndrome, autosomal recessive [NCBI] 6.59199e-05
ehlers-danlos syndrome, type iv, autosomal dominant [NCBI] 6.33845e-05
BGS [NCBI] 6.10739e-05
RBS [NCBI] 5.99915e-05
RTS [NCBI] 5.26699e-05
FOP [NCBI] 5.18877e-05
IHH [NCBI] 5.10734e-05
COMP [NCBI] 4.91415e-05
NPS [NCBI] 4.57813e-05
FAM20C [NCBI] 4.54163e-05
WNT7A [NCBI] 4.22781e-05
SDS [NCBI] 4.19126e-05
TD1 [NCBI] 4.14083e-05
PTH [NCBI] 3.8028e-05
TBX5 [NCBI] 3.75051e-05
MAS [NCBI] 3.53132e-05
CDLS1 [NCBI] 3.53132e-05
ACP5 [NCBI] 3.41404e-05
SLC4A1 [NCBI] 2.88019e-05
FGFR1 [NCBI] 2.389e-05
RA [NCBI] 2.19101e-05
WBS [NCBI] 1.73917e-05
G6PD [NCBI] 9.44329e-06
TNF [NCBI] 2.29814e-08
VEGF [NCBI] 3.96204e-10



Database Center for Life Science