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01 Ectromelia [NCBI]

Gene


 Gene Link Information
Gain		 01
HFM [NCBI] 0.000291504
ESCO2 [NCBI] 8.70144e-05
SNX3 [NCBI] 1.47485e-05
NR2E1 [NCBI] 1.36815e-05
WNT3 [NCBI] 1.2857e-05
SALL4 [NCBI] 1.14735e-05
ROR2 [NCBI] 1.1402e-05
WNT7A [NCBI] 1.12673e-05
FGF10 [NCBI] 1.03396e-05
GLI2 [NCBI] 1.0195e-05
GLI3 [NCBI] 9.27786e-06
HOXA9 [NCBI] 9.03255e-06
KLRK1 [NCBI] 7.87647e-06
BMP7 [NCBI] 7.21788e-06
CKAP4 [NCBI] 7.21788e-06
TNF [NCBI] 1.66616e-06



OMIM


 OMIM Link Information
gain		 01
thrombocytopenia-absent radius syndrome [NCBI] 0.00216872
RBS [NCBI] 0.00166055
sc phocomelia syndrome [NCBI] 0.00109551
polydactyly, preaxial iii [NCBI] 0.000993831
microcephaly-micromelia syndrome [NCBI] 0.000993831
ulna and fibula, absence of, with severe limb deficiency [NCBI] 0.000949311
SHFM1 [NCBI] 0.000774856
nievergelt syndrome [NCBI] 0.000641003
femur, unilateral bifid, with monodactylous ectrodactyly [NCBI] 0.000570168
tibia, hypoplasia of, with polydactyly [NCBI] 0.000485191
ESCO2 [NCBI] 0.000469749
kyphomelic dysplasia [NCBI] 0.000469717
OFD4 [NCBI] 0.000469717
tetra-amelia, autosomal recessive [NCBI] 0.00045731
constricting bands, congenital [NCBI] 0.000431005
tetra-amelia, x-linked [NCBI] 0.000342666
brachial amelia, forebrain defects, and facial clefts [NCBI] 0.000342666
poland syndrome [NCBI] 0.000293583
femur-fibula-ulna syndrome [NCBI] 0.000288144
urogenital adysplasia, hereditary [NCBI] 0.000251968
tetra-amelia with ectodermal dysplasia and lacrimal duct abnormalities [NCBI] 0.000228234
HOS [NCBI] 0.000218753
splenogonadal fusion with limb defects and micrognathia [NCBI] 0.000173727
HFM [NCBI] 0.000170403
tibial hemimelia [NCBI] 0.000166381
chondrodysplasia, grebe type [NCBI] 0.000147228
CDLS1 [NCBI] 0.000118077
amelia, autosomal recessive [NCBI] 0.000114013
aphalangy with hemivertebrae [NCBI] 0.000114013
phocomelia-ectrodactyly, ear malformation, deafness, and sinus arrhythmia [NCBI] 9.15549e-05
dk phocomelia syndrome [NCBI] 9.15549e-05
renal dysplasia-limb defects syndrome [NCBI] 9.15549e-05
limb defects, distal transverse, with mental retardation and spasticity [NCBI] 8.3087e-05
ectrodactyly [NCBI] 7.35111e-05
SNX3 [NCBI] 7.32984e-05
aglossia-adactylia [NCBI] 7.02613e-05
fibular aplasia or hypoplasia, femoral bowing and poly-, syn-, and oligodactyly [NCBI] 7.02613e-05
WNT3 [NCBI] 6.99214e-05
rokitansky-kuster-hauser syndrome [NCBI] 6.52515e-05
vacterl association with hydrocephalus [NCBI] 6.52515e-05
WNT7A [NCBI] 6.37462e-05
FANCB [NCBI] 6.37462e-05
vacterl association with hydrocephalus, x-linked [NCBI] 6.32341e-05
atrial septal defect with atrioventricular conduction defects [NCBI] 6.32341e-05
BMP7 [NCBI] 6.23221e-05
LMBR1 [NCBI] 5.99713e-05
PPD2 [NCBI] 5.83723e-05
acheiropody [NCBI] 5.70341e-05
disorganization, mouse, homolog of [NCBI] 5.70341e-05
SYM1 [NCBI] 5.58001e-05
NKX2E [NCBI] 5.28281e-05
UMS [NCBI] 4.99225e-05
BGS [NCBI] 4.62927e-05
diastrophic dysplasia [NCBI] 4.56583e-05
TRPS2 [NCBI] 3.76186e-05
CES [NCBI] 3.46327e-05
WHS [NCBI] 2.60483e-05
SHH [NCBI] 2.50287e-05
FA [NCBI] 2.96622e-06
TNF [NCBI] 7.96201e-07



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