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01 Clubfoot [NCBI]

Gene


 Gene Link Information
Gain		 01
SLC26A2 [NCBI] 2.3263e-05
CASP10 [NCBI] 2.29305e-05
FHL1 [NCBI] 1.31776e-05
TPM2 [NCBI] 1.26649e-05
LAMA2 [NCBI] 1.2103e-05
HOXD10 [NCBI] 1.20249e-05
WNT7A [NCBI] 1.1744e-05
HOXD13 [NCBI] 1.05065e-05
NAIP [NCBI] 9.15985e-06
CASP8 [NCBI] 8.95717e-06
APAF1 [NCBI] 8.32523e-06
NAT1 [NCBI] 8.29902e-06
BID [NCBI] 8.16565e-06
SMN1 [NCBI] 7.75439e-06
DMPK [NCBI] 7.413e-06
CFLAR [NCBI] 7.24151e-06
BCL2 [NCBI] 7.09855e-06
NAT2 [NCBI] 6.75808e-06
CASP9 [NCBI] 5.58238e-06
MTHFR [NCBI] 5.0703e-06
CASP3 [NCBI] 3.63354e-06



OMIM


 OMIM Link Information
gain		 01
gordon syndrome [NCBI] 0.00283118
larsen syndrome, recessive [NCBI] 0.00215269
schinzel-giedion midface-retraction syndrome [NCBI] 0.00166184
metatarsus varus, type i [NCBI] 0.000959695
pena-shokeir syndrome, type i [NCBI] 0.000691189
acromial dimples [NCBI] 0.000607072
adducted thumb-clubfoot syndrome [NCBI] 0.000607072
clubfoot [NCBI] 0.000605852
SPG5A [NCBI] 0.000468835
megalocornea-mental retardation syndrome [NCBI] 0.000436268
DBQD [NCBI] 0.000422299
LRS1 [NCBI] 0.000338288
robin sequence with cleft mandible and limb anomalies [NCBI] 0.000326091
DA2A [NCBI] 0.000282676
FRNS [NCBI] 0.000280333
FFS [NCBI] 0.000253238
SHFM1 [NCBI] 0.000245359
AOS [NCBI] 0.000234292
whistling face syndrome, recessive form [NCBI] 0.000164165
DA1 [NCBI] 0.000156918
multiple pterygium syndrome, escobar variant [NCBI] 0.00014602
diastrophic dysplasia [NCBI] 0.000127305
erythema of acral regions [NCBI] 0.000120535
ulnar hypoplasia with mental retardation [NCBI] 0.000120535
brachydactyly-distal symphalangism syndrome [NCBI] 0.000120535
crane-heise syndrome [NCBI] 9.80716e-05
short stature, auditory canal atresia, mandibular hypoplasia, skeletal abnormalities [NCBI] 9.80716e-05
lambert syndrome [NCBI] 9.80716e-05
AMC [NCBI] 9.52551e-05
aminopterin syndrome sine aminopterin [NCBI] 8.41001e-05
frank-ter haar syndrome [NCBI] 7.32571e-05
BDE [NCBI] 7.17398e-05
EDM4 [NCBI] 6.97176e-05
LAMA2 [NCBI] 6.74106e-05
SLC26A2 [NCBI] 6.67002e-05
COFS1 [NCBI] 6.00385e-05
enchondromatosis, multiple [NCBI] 5.90341e-05
abdominal muscles, absence of, with urinary tract abnormality and cryptorchidism [NCBI] 5.71979e-05
ATRX [NCBI] 5.67433e-05
dystrophia myotonica 1 [NCBI] 5.67327e-05
bethlem myopathy [NCBI] 5.55524e-05
BIRC1 [NCBI] 5.45026e-05
MDC1A [NCBI] 5.40621e-05
PPS [NCBI] 5.27003e-05
MRXHF1 [NCBI] 5.20612e-05
SPG3A [NCBI] 4.50992e-05
CES [NCBI] 4.09124e-05
EDMD [NCBI] 4.09124e-05
MKS1 [NCBI] 3.86475e-05
AHO [NCBI] 3.06915e-05
CF [NCBI] 2.48668e-05
SLOS [NCBI] 1.89405e-05
PWS [NCBI] 5.03843e-06



Database Center for Life Science