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MeSH keywords -> Related genes, diseases (OMIM)


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01 Fetal Diseases [NCBI]

Gene


 Gene Link Information
Gain		 01
VUR [NCBI] 0.00153615
DHS [NCBI] 0.000478114
DWS [NCBI] 0.00046776
AFP [NCBI] 0.00038693
FGFR3 [NCBI] 5.77391e-05
CFTR [NCBI] 4.07203e-05
ACHE [NCBI] 3.99099e-05
AVP [NCBI] 3.95197e-05
SLC26A2 [NCBI] 2.84644e-05
HADHA [NCBI] 2.54616e-05
ZIC2 [NCBI] 2.45015e-05
TROVE2 [NCBI] 2.43371e-05
HBB [NCBI] 1.87233e-05
CHRND [NCBI] 1.7543e-05
EPO [NCBI] 1.74759e-05
AGXT2L1 [NCBI] 1.64034e-05
NPPA [NCBI] 1.62723e-05
HNF1B [NCBI] 1.62432e-05
PAH [NCBI] 1.59865e-05
CHRNA1 [NCBI] 1.54928e-05
FMR1 [NCBI] 1.53633e-05
RHD [NCBI] 1.4869e-05
KCNJ1 [NCBI] 1.36792e-05
SIX3 [NCBI] 1.36792e-05
TGIF1 [NCBI] 1.34843e-05
SFTPC [NCBI] 1.29589e-05
ASPA [NCBI] 1.2724e-05
AMBP [NCBI] 1.16614e-05
FKTN [NCBI] 1.14749e-05
SOX2 [NCBI] 1.13722e-05
ADA [NCBI] 1.07803e-05
PIH [NCBI] 1.00192e-05
GLE1 [NCBI] 9.54726e-06
MRPS22 [NCBI] 9.54726e-06
SLMAP [NCBI] 9.11407e-06
PAEP [NCBI] 9.03815e-06
HADHB [NCBI] 8.76901e-06
CDC5L [NCBI] 8.76901e-06
PKD1L1 [NCBI] 8.76901e-06
GJD2 [NCBI] 8.76901e-06
ACP2 [NCBI] 8.76901e-06
MTRR [NCBI] 8.59597e-06
ATP7A [NCBI] 8.46803e-06
SYNM [NCBI] 8.23672e-06
SLC27A4 [NCBI] 8.23672e-06
TALDO1 [NCBI] 8.23672e-06
HBZ [NCBI] 8.0222e-06
MTHFR [NCBI] 7.89866e-06
CHRNB1 [NCBI] 7.6604e-06
NDUFV1 [NCBI] 7.50478e-06
SCO1 [NCBI] 7.36221e-06
FLNB [NCBI] 7.36221e-06
ALPI [NCBI] 7.36221e-06
RAPSN [NCBI] 7.23069e-06
CD109 [NCBI] 7.23069e-06
DLL3 [NCBI] 7.10863e-06
HTT [NCBI] 7.055e-06
GBE1 [NCBI] 6.99476e-06
ARSE [NCBI] 6.99476e-06
TUBA1A [NCBI] 6.99476e-06
PTS [NCBI] 6.88806e-06
TREX1 [NCBI] 6.78769e-06
GLDC [NCBI] 6.69294e-06
SLC17A5 [NCBI] 6.60322e-06
NIPBL [NCBI] 6.51802e-06
TRIM21 [NCBI] 6.43692e-06
PAX6 [NCBI] 6.39643e-06
OMP [NCBI] 6.28555e-06
SALL4 [NCBI] 6.28555e-06
CHD7 [NCBI] 6.21468e-06
SHH [NCBI] 6.05983e-06
FGD1 [NCBI] 6.01839e-06
PTPN11 [NCBI] 5.97422e-06
EDN3 [NCBI] 5.95775e-06
MTF1 [NCBI] 5.89922e-06
MTM1 [NCBI] 5.84267e-06
GAMT [NCBI] 5.84267e-06
MLLT10 [NCBI] 5.78796e-06
PF4 [NCBI] 5.73995e-06
CYP11B1 [NCBI] 5.73499e-06
SFRP4 [NCBI] 5.68364e-06
HSD17B4 [NCBI] 5.63383e-06
CA2 [NCBI] 5.53845e-06
ITGA6 [NCBI] 5.49273e-06
T [NCBI] 5.40489e-06
OXCT2 [NCBI] 5.36266e-06
IKBKAP [NCBI] 5.32147e-06
NFKB2 [NCBI] 5.28127e-06
SLC5A1 [NCBI] 5.28127e-06
APBA1 [NCBI] 5.2037e-06
MSX1 [NCBI] 5.2037e-06
DHCR7 [NCBI] 5.09376e-06
ABCA3 [NCBI] 5.09376e-06
GLB1 [NCBI] 5.02433e-06
GSTA5 [NCBI] 4.89367e-06
ALDH5A1 [NCBI] 4.89367e-06
FKRP [NCBI] 4.86257e-06
INHA [NCBI] 4.86257e-06
SPINK5 [NCBI] 4.77265e-06
F2RL3 [NCBI] 4.74374e-06
ALDH3A2 [NCBI] 4.71533e-06
L1CAM [NCBI] 4.71533e-06
SCN9A [NCBI] 4.65995e-06
ADAM12 [NCBI] 4.63295e-06
ITGB4 [NCBI] 4.52921e-06
KRT10 [NCBI] 4.40821e-06
HES1 [NCBI] 4.38505e-06
CD68 [NCBI] 4.38099e-06
GPI [NCBI] 4.31752e-06
MME [NCBI] 4.31752e-06
GJB6 [NCBI] 4.07259e-06
MLL [NCBI] 3.9645e-06
AIRE [NCBI] 3.89374e-06
FN1 [NCBI] 3.86026e-06
PAFAH1B1 [NCBI] 3.82748e-06
RPE65 [NCBI] 3.81135e-06
ADH1C [NCBI] 3.81135e-06
PROC [NCBI] 3.71784e-06
UBE3A [NCBI] 3.70279e-06
ESD [NCBI] 3.65846e-06
APRT [NCBI] 3.55969e-06
SPINT2 [NCBI] 3.53258e-06
EPOR [NCBI] 3.47975e-06
FGF3 [NCBI] 3.47975e-06
RUNX2 [NCBI] 3.46682e-06
RELN [NCBI] 3.44128e-06
POU1F1 [NCBI] 3.42866e-06
FANCC [NCBI] 3.42866e-06
HBA1 [NCBI] 3.41615e-06
PSAP [NCBI] 3.40374e-06
HDC [NCBI] 3.39143e-06
FGB [NCBI] 3.39143e-06
NGFR [NCBI] 3.26215e-06
CD40LG [NCBI] 3.25092e-06
VCAN [NCBI] 3.16397e-06
COL2A1 [NCBI] 3.1223e-06
CRH [NCBI] 3.1223e-06
MAP2 [NCBI] 2.89403e-06
DMD [NCBI] 2.89403e-06
SMN2 [NCBI] 2.81675e-06
FGFR2 [NCBI] 2.79187e-06
SRY [NCBI] 2.76741e-06
GNAS [NCBI] 2.67348e-06
TRH [NCBI] 2.67296e-06
NOTCH3 [NCBI] 2.6584e-06
ETS1 [NCBI] 2.64348e-06
AR [NCBI] 2.64192e-06
GFAP [NCBI] 2.6386e-06
ESR2 [NCBI] 2.46907e-06
FABP7 [NCBI] 2.41121e-06
MPL [NCBI] 2.38625e-06
KCNH6 [NCBI] 2.31395e-06
CYBB [NCBI] 2.30809e-06
SMN1 [NCBI] 2.25648e-06
NOTCH1 [NCBI] 2.21219e-06
SCGB1A1 [NCBI] 2.19595e-06
MATN1 [NCBI] 2.14837e-06
ITGB3 [NCBI] 2.13803e-06
ETV6 [NCBI] 2.13288e-06
KCNQ1 [NCBI] 2.12266e-06
PGF [NCBI] 2.00108e-06
GDNF [NCBI] 1.96898e-06
DMPK [NCBI] 1.95546e-06
POMC [NCBI] 1.88993e-06
NKX2-1 [NCBI] 1.82762e-06
BTK [NCBI] 1.79561e-06
ALK [NCBI] 1.7453e-06
WAS [NCBI] 1.71533e-06
ERCC2 [NCBI] 1.71164e-06
LAMB3 [NCBI] 1.69697e-06
TFPI [NCBI] 1.65051e-06
NPY [NCBI] 1.58983e-06
MBP [NCBI] 1.52107e-06
UMOD [NCBI] 1.50864e-06
CCND1 [NCBI] 1.49936e-06
ENG [NCBI] 1.4871e-06
BMP2 [NCBI] 1.21806e-06
TLR2 [NCBI] 1.2039e-06
STAT1 [NCBI] 1.05603e-06
MOG [NCBI] 1.03607e-06
GJB2 [NCBI] 1.02624e-06
VWF [NCBI] 8.70736e-07
CST3 [NCBI] 7.60112e-07
JAK2 [NCBI] 6.72367e-07
VEGFA [NCBI] 6.61031e-07
TNF [NCBI] 5.79036e-07
APC [NCBI] 5.5349e-07
CALCA [NCBI] 5.33559e-07
VDR [NCBI] 5.33559e-07
TG [NCBI] 4.57183e-07
TLR4 [NCBI] 4.32431e-07
EGF [NCBI] 3.39341e-07
EGFR [NCBI] 2.49309e-07
PTGS2 [NCBI] 2.39257e-07
IL1RN [NCBI] 1.51433e-07
NOS2 [NCBI] 1.4167e-07
HIF1A [NCBI] 1.27642e-07
CTNNB1 [NCBI] 5.08452e-08
TGFB1 [NCBI] 2.46618e-08
APOE [NCBI] 1.68208e-08



OMIM


 OMIM Link Information
gain		 01
pena-shokeir syndrome, type i [NCBI] 0.00448058
renal hamartomas, nephroblastomatosis, and fetal gigantism [NCBI] 0.00211119
AFP [NCBI] 0.00141985
DWS [NCBI] 0.00113953
MRD [NCBI] 0.00113726
exstrophy of bladder [NCBI] 0.00105049
DHS [NCBI] 0.00103277
myeloproliferative syndrome, transient [NCBI] 0.000832697
cardiomyopathy, fatal fetal, due to myocardial calcification [NCBI] 0.000786952
succinic acidemia [NCBI] 0.000786952
varadi-papp syndrome [NCBI] 0.000663813
NLS [NCBI] 0.000492677
faciodigitogenital syndrome, recessive [NCBI] 0.000488822
EPV [NCBI] 0.000488822
valinemia [NCBI] 0.000488822
campomelia, cumming type [NCBI] 0.000436447
renal-hepatic-pancreatic dysplasia with dandy-walker cyst [NCBI] 0.000436447
dandy-walker malformation with mental retardation, basal ganglia disease, and seizures [NCBI] 0.000436447
holoprosencephaly [NCBI] 0.000413618
OSCS [NCBI] 0.000367161
lethal congenital contracture syndrome 1 [NCBI] 0.000367161
metatropic dwarfism [NCBI] 0.000341884
short rib-polydactyly syndrome, type i [NCBI] 0.000341884
urogenital adysplasia, hereditary [NCBI] 0.000334531
short rib-polydactyly syndrome, type iii [NCBI] 0.000270586
BZX [NCBI] 0.000257323
microcephalic osteodysplastic primordial dwarfism, type ii [NCBI] 0.000257323
progeroid syndrome, neonatal [NCBI] 0.000245256
short rib-polydactyly syndrome, type iv [NCBI] 0.000245256
intestinal atresia, multiple [NCBI] 0.000245256
vitamin k-dependent clotting factors, combined deficiency of, 1 [NCBI] 0.000238324
AMCN [NCBI] 0.0002342
chondrodysplasia punctata, autosomal dominant [NCBI] 0.000228349
ACG1A [NCBI] 0.00022401
BWS [NCBI] 0.000194661
robinow syndrome, autosomal dominant [NCBI] 0.000189897
SLE [NCBI] 0.00018774
TD1 [NCBI] 0.000168738
SLOS [NCBI] 0.000161748
diaphragmatic hernia, congenital [NCBI] 0.000157533
hydrops fetalis, idiopathic [NCBI] 0.000155777
tight skin contracture syndrome, lethal [NCBI] 0.000152401
VUR1 [NCBI] 0.000152032
CTNS [NCBI] 0.000144986
coffin-siris syndrome [NCBI] 0.000141796
DMD [NCBI] 0.000140131
krabbe disease [NCBI] 0.000134128
FRNS [NCBI] 0.000128088
PKS [NCBI] 0.00011867
phenylketonuria [NCBI] 0.000114681
FGFR3 [NCBI] 0.000113676
CDC5L [NCBI] 0.000109652
walker-warburg syndrome [NCBI] 0.000108065
ATD1 [NCBI] 0.000105292
pseudotrisomy 13 syndrome [NCBI] 0.000102594
trifunctional protein deficiency [NCBI] 9.95455e-05
ACHE [NCBI] 9.88955e-05
EPHX1 [NCBI] 9.86016e-05
lymphedema, hereditary, i [NCBI] 9.67685e-05
GUSB [NCBI] 9.5192e-05
ACH [NCBI] 9.46925e-05
tibia, absence or hypoplasia of, with polydactyly, retrocerebellar arachnoid cyst, and other anomalies [NCBI] 9.33118e-05
facial dysmorphism with multiple malformations [NCBI] 9.33118e-05
osteosclerotic chondrodysplasia, lethal, with intracellular inclusions [NCBI] 9.33118e-05
acid phosphatase deficiency [NCBI] 9.33118e-05
cystic kidney disease with ventriculomegaly [NCBI] 9.33118e-05
COFS2 [NCBI] 9.33118e-05
COXPD5 [NCBI] 9.33118e-05
baby rattle pelvis dysplasia [NCBI] 9.33118e-05
microcephaly, severe, with skeletal anomalies including posterior rib-gap defects [NCBI] 9.33118e-05
USF2 [NCBI] 8.70647e-05
AMC [NCBI] 8.34251e-05
long-chain 3-hydroxyacyl-coa dehydrogenase deficiency [NCBI] 7.76013e-05
TS [NCBI] 7.68295e-05
SMA1 [NCBI] 7.55207e-05
AVSD [NCBI] 7.38939e-05
HBZ [NCBI] 7.33063e-05
epidermolysis bullosa with pyloric atresia [NCBI] 7.23864e-05
AVP [NCBI] 7.21119e-05
mucopolysaccharidosis type iiia [NCBI] 7.12133e-05
MCOPCB4 [NCBI] 7.08904e-05
convulsive disorder, familial, with prenatal or early onset [NCBI] 7.08904e-05
cahmr syndrome [NCBI] 7.08904e-05
sialuria, finnish type [NCBI] 7.00848e-05
AHC [NCBI] 6.69369e-05
HSAS [NCBI] 6.69369e-05
HCH [NCBI] 6.40944e-05
MDLS [NCBI] 6.32055e-05
fetal akinesia syndrome, x-linked [NCBI] 6.24595e-05
aarskog syndrome [NCBI] 6.24595e-05
xeroderma pigmentosum ix [NCBI] 6.24595e-05
hypophosphatasia, infantile [NCBI] 6.2343e-05
HPE5 [NCBI] 5.70024e-05
anal atresia, hypospadias, and penoscrotal inversion [NCBI] 5.70024e-05
chylothorax, congenital [NCBI] 5.70024e-05
dehydrated hereditary stomatocytosis, pseudohyperkalemia, and perinatal edema [NCBI] 5.70024e-05
nuchal bleb, familial [NCBI] 5.70024e-05
FIDD [NCBI] 5.70024e-05
LIS2 [NCBI] 5.70024e-05
PHS [NCBI] 5.69388e-05
XPA [NCBI] 5.62445e-05
HSAN3 [NCBI] 5.4259e-05
polycystic kidneys [NCBI] 5.39397e-05
recombinant chromosome 8 syndrome [NCBI] 5.29577e-05
paroxysmal extreme pain disorder [NCBI] 5.29577e-05
MTF1 [NCBI] 5.05219e-05
bartter syndrome, antenatal, type 1 [NCBI] 4.97449e-05
mevalonic aciduria [NCBI] 4.97449e-05
VEGF [NCBI] 4.96299e-05
MTM1 [NCBI] 4.95711e-05
wolman disease [NCBI] 4.83866e-05
MKS1 [NCBI] 4.74992e-05
xeroderma pigmentosum, complementation group e [NCBI] 4.70818e-05
cataract, microcephaly, failure to thrive, kyphoscoliosis syndrome [NCBI] 4.70818e-05
OPTB5 [NCBI] 4.70818e-05
pancreas, annular [NCBI] 4.70818e-05
factor vii deficiency [NCBI] 4.58814e-05
MRPS22 [NCBI] 4.53358e-05
carnitine palmitoyltransferase i deficiency [NCBI] 4.48093e-05
microcephaly with spastic quadriplegia [NCBI] 4.48093e-05
oeis complex [NCBI] 4.48093e-05
epidermolysis bullosa herpetiformis, dowling-meara type [NCBI] 4.28289e-05
methylmalonic aciduria, cbla type [NCBI] 4.28289e-05
martsolf syndrome [NCBI] 4.28289e-05
SLC12A1 [NCBI] 4.19734e-05
F2RL3 [NCBI] 4.19734e-05
hydrops-ectopic calcification-moth-eaten skeletal dysplasia [NCBI] 4.10753e-05
XPG [NCBI] 4.10753e-05
succinyl-coa:3-oxoacid coa transferase deficiency [NCBI] 4.10753e-05
GGM [NCBI] 4.10753e-05
adrenal hyperplasia, congenital, due to 21-hydroxylase deficiency [NCBI] 4.10315e-05
shprintzen-goldberg craniosynostosis syndrome [NCBI] 3.95028e-05
de sanctis-cacchione syndrome [NCBI] 3.95028e-05
XPV [NCBI] 3.95028e-05
gaucher disease, perinatal lethal [NCBI] 3.95028e-05
GCSH [NCBI] 3.94771e-05
TSD [NCBI] 3.90311e-05
EGF [NCBI] 3.81082e-05
XPF [NCBI] 3.80783e-05
CHD7 [NCBI] 3.74909e-05
CPI [NCBI] 3.70658e-05
CF [NCBI] 3.70299e-05
LQT3 [NCBI] 3.67772e-05
multiple pterygium syndrome, lethal type [NCBI] 3.67772e-05
hydrocephalus [NCBI] 3.67772e-05
FLNB [NCBI] 3.58418e-05
SLC5A1 [NCBI] 3.58418e-05
HHS [NCBI] 3.55802e-05
langer mesomelic dysplasia [NCBI] 3.55802e-05
chromosome 5q deletion syndrome [NCBI] 3.55802e-05
CTHM [NCBI] 3.44726e-05
gaucher disease, type ii [NCBI] 3.44726e-05
d-bifunctional protein deficiency [NCBI] 3.44726e-05
MTRR [NCBI] 3.44323e-05
CDG2C [NCBI] 3.34424e-05
COFS1 [NCBI] 3.34424e-05
EPD [NCBI] 3.34424e-05
bartter syndrome, antenatal, type 2 [NCBI] 3.34424e-05
XPD [NCBI] 3.34424e-05
NCIE1 [NCBI] 3.34424e-05
SFRP4 [NCBI] 3.32018e-05
ALDH1A2 [NCBI] 3.32018e-05
RHD [NCBI] 3.32018e-05
alpers diffuse degeneration of cerebral gray matter with hepatic cirrhosis [NCBI] 3.24798e-05
succinic semialdehyde dehydrogenase deficiency [NCBI] 3.24798e-05
hydatidiform mole [NCBI] 3.24798e-05
hypercholesterolemia, autosomal dominant [NCBI] 3.22165e-05
AMT [NCBI] 3.21104e-05
HPRT1 [NCBI] 3.19399e-05
NETH [NCBI] 3.1577e-05
DRRS [NCBI] 3.1577e-05
dystrophia myotonica 1 [NCBI] 3.15305e-05
IKBKAP [NCBI] 3.11301e-05
abdominal muscles, absence of, with urinary tract abnormality and cryptorchidism [NCBI] 3.07272e-05
heart block, congenital [NCBI] 3.07272e-05
JBS [NCBI] 3.07272e-05
adrenal hyperplasia, congenital, due to steroid 11-beta-hydroxylase deficiency [NCBI] 2.99249e-05
TTDP [NCBI] 2.99249e-05
klippel-trenaunay-weber syndrome [NCBI] 2.98907e-05
PGF [NCBI] 2.94267e-05
DLL3 [NCBI] 2.94267e-05
RTD [NCBI] 2.91653e-05
AGS1 [NCBI] 2.91653e-05
FLT4 [NCBI] 2.86767e-05
SLC17A5 [NCBI] 2.86767e-05
TNF [NCBI] 2.82004e-05
HADHA [NCBI] 2.79815e-05
DLD [NCBI] 2.79815e-05
mucopolysaccharidosis type iiib [NCBI] 2.77585e-05
GACI [NCBI] 2.77585e-05
SALL4 [NCBI] 2.73337e-05
SLC2A1 [NCBI] 2.67274e-05
MME [NCBI] 2.67274e-05
FN1 [NCBI] 2.61577e-05
POU1F1 [NCBI] 2.61577e-05
EGFR [NCBI] 2.61007e-05
diastrophic dysplasia [NCBI] 2.58831e-05
TPI1 [NCBI] 2.56206e-05
GLDC [NCBI] 2.56206e-05
infantile sialic acid storage disorder [NCBI] 2.53108e-05
EDN3 [NCBI] 2.51126e-05
hyperglycerolemia [NCBI] 2.47615e-05
OPTB1 [NCBI] 2.47615e-05
PTS [NCBI] 2.46308e-05
IP [NCBI] 2.43601e-05
transcobalamin ii deficiency [NCBI] 2.37361e-05
glycogen storage disease iv [NCBI] 2.37259e-05
OMP [NCBI] 2.33192e-05
faciogenital dysplasia [NCBI] 2.32367e-05
niemann-pick disease, type a [NCBI] 2.2765e-05
MADD [NCBI] 2.2765e-05
fraser syndrome [NCBI] 2.2765e-05
SMAX1 [NCBI] 2.2743e-05
GPI [NCBI] 2.2508e-05
mucopolysaccharidosis type vii [NCBI] 2.23096e-05
EFE [NCBI] 2.23096e-05
ETV6 [NCBI] 2.2171e-05
ERCC2 [NCBI] 2.2171e-05
MTM1 [NCBI] 2.2171e-05
XPC [NCBI] 2.2171e-05
ERCC5 [NCBI] 2.2171e-05
MSD [NCBI] 2.18696e-05
FMR1 [NCBI] 2.17423e-05
hyperoxaluria, primary, type i [NCBI] 2.1444e-05
CMTX1 [NCBI] 2.10321e-05
DMD [NCBI] 2.10146e-05
homocystinuria due to deficiency of n(5,10)-methylenetetrahydrofolate reductase activity [NCBI] 2.0633e-05
FIH [NCBI] 2.0633e-05
GAMT [NCBI] 2.05297e-05
PAEP [NCBI] 2.05297e-05
charge syndrome [NCBI] 2.02461e-05
XLP1 [NCBI] 2.02461e-05
MEB [NCBI] 2.02461e-05
GLB1 [NCBI] 1.99486e-05
AGT [NCBI] 1.99486e-05
EVC [NCBI] 1.98708e-05
fragile x mental retardation syndrome [NCBI] 1.97231e-05
FANCC [NCBI] 1.9403e-05
ASPA [NCBI] 1.91423e-05
SLC11A2 [NCBI] 1.91423e-05
PSAP [NCBI] 1.91423e-05
ATP7A [NCBI] 1.8889e-05
L1CAM [NCBI] 1.8889e-05
ADA [NCBI] 1.88119e-05
MG [NCBI] 1.84224e-05
MTATP6 [NCBI] 1.84033e-05
SMN2 [NCBI] 1.81702e-05
pyruvate kinase deficiency of red cells [NCBI] 1.81478e-05
CMTC [NCBI] 1.75216e-05
DGS [NCBI] 1.73954e-05
SCIDX1 [NCBI] 1.69268e-05
THRB [NCBI] 1.66933e-05
AN2 [NCBI] 1.60879e-05
SCN5A [NCBI] 1.59513e-05
methemoglobinemia due to deficiency of methemoglobin reductase [NCBI] 1.59513e-05
CLN3 [NCBI] 1.58213e-05
mucopolysaccharidosis type iva [NCBI] 1.57755e-05
PI [NCBI] 1.56423e-05
CSA [NCBI] 1.55608e-05
neuraminidase deficiency [NCBI] 1.55608e-05
bare lymphocyte syndrome, type ii [NCBI] 1.53063e-05
CHM [NCBI] 1.53063e-05
ED1 [NCBI] 1.53063e-05
BPES [NCBI] 1.48139e-05
FCMD [NCBI] 1.45757e-05
aortic valve disease [NCBI] 1.41144e-05
protein c deficiency, congenital thrombotic disease due to [NCBI] 1.39143e-05
ornithine transcarbamylase deficiency, hyperammonemia due to [NCBI] 1.38909e-05
osteogenesis imperfecta, type iia [NCBI] 1.38909e-05
MTHFR [NCBI] 1.36416e-05
EPO [NCBI] 1.35483e-05
glioma of brain, familial [NCBI] 1.34575e-05
TSC2 [NCBI] 1.32492e-05
LNS [NCBI] 1.24469e-05
NGFR [NCBI] 1.24033e-05
ND [NCBI] 1.22563e-05
GNAS [NCBI] 1.18511e-05
ichthyosis, x-linked [NCBI] 1.16409e-05
CHH [NCBI] 1.15282e-05
GBA [NCBI] 1.14365e-05
PF4 [NCBI] 1.13778e-05
EPOR [NCBI] 1.114e-05
metachromatic leukodystrophy [NCBI] 1.0851e-05
LPI [NCBI] 1.0689e-05
SLS [NCBI] 1.00681e-05
CCD [NCBI] 9.48718e-06
ATM [NCBI] 9.42325e-06
APOE [NCBI] 9.32762e-06
menkes disease [NCBI] 9.21059e-06
PKD1 [NCBI] 8.9098e-06
WHS [NCBI] 8.68304e-06
HDC [NCBI] 8.17527e-06
TLR2 [NCBI] 7.92755e-06
NS1 [NCBI] 7.83453e-06
AR [NCBI] 7.70821e-06
APRT [NCBI] 7.63098e-06
AHO [NCBI] 7.60801e-06
PTHLH [NCBI] 6.54117e-06
RP [NCBI] 6.35655e-06
hemophilia a [NCBI] 6.196e-06
CDLS1 [NCBI] 5.9236e-06
FRDA [NCBI] 5.9236e-06
AT [NCBI] 5.60364e-06
DBA [NCBI] 5.49904e-06
HBB [NCBI] 4.39724e-06
FGF7 [NCBI] 4.01518e-06
FA [NCBI] 3.6756e-06
HD [NCBI] 3.67391e-06
CMH [NCBI] 3.46212e-06
SRS [NCBI] 2.16804e-06
POMC [NCBI] 1.86926e-06
CFTR [NCBI] 1.78313e-06
WBS [NCBI] 1.49615e-06
TLR4 [NCBI] 1.44152e-06
CHS [NCBI] 1.43639e-06
ACPP [NCBI] 1.24003e-06
G6PD [NCBI] 1.14484e-06
TFPI [NCBI] 9.52574e-07
ALD [NCBI] 8.14056e-07
MBP [NCBI] 4.66084e-07
NPY [NCBI] 4.06122e-07
TG [NCBI] 3.91771e-07
GFAP [NCBI] 2.2695e-07
VDR [NCBI] 2.21711e-07
CRH [NCBI] 1.47046e-07
MUC1 [NCBI] 1.22567e-07
thrombocytopenic purpura, autoimmune [NCBI] 4.76346e-08
AS [NCBI] 1.65077e-08
WAS [NCBI] 7.69433e-09



Database Center for Life Science