|
OMIM |
Link |
Information gain |
01 |
|
fragile x mental retardation syndrome
|
[NCBI]
|
0.00693551
|
|
|
MRX1
|
[NCBI]
|
0.0027612
|
|
|
oligosynaptic infertility
|
[NCBI]
|
0.00266912
|
|
|
AIC
|
[NCBI]
|
0.00257338
|
|
|
GBY
|
[NCBI]
|
0.00230812
|
|
|
GCY
|
[NCBI]
|
0.00207285
|
|
|
MCOPS1
|
[NCBI]
|
0.001964581
|
|
|
OFD8
|
[NCBI]
|
0.001513327
|
|
|
persistent hyperplastic primary vitreous, autosomal dominant
|
[NCBI]
|
0.00133075
|
|
|
parkinsonism, early-onset, with mental retardation
|
[NCBI]
|
0.00133075
|
|
|
brooks-wisniewski-brown syndrome
|
[NCBI]
|
0.00133075
|
|
|
MAFD2
|
[NCBI]
|
0.001227014
|
|
|
SRY
|
[NCBI]
|
0.001204711
|
|
|
terminal osseous dysplasia and pigmentary defects
|
[NCBI]
|
0.001196605
|
|
|
mental retardation with optic atrophy, deafness, and seizures
|
[NCBI]
|
0.001150297
|
|
|
auditory neuropathy, x-linked, 1, with peripheral sensory neuropathy
|
[NCBI]
|
0.001150297
|
|
|
SPG16
|
[NCBI]
|
0.001150297
|
|
|
MRX20
|
[NCBI]
|
0.001150297
|
|
|
MRX2
|
[NCBI]
|
0.001150297
|
|
|
x inactivation, familial skewed, 2
|
[NCBI]
|
0.001120735
|
|
|
MCOPS4
|
[NCBI]
|
0.001097646
|
|
|
persistent hyperplastic primary vitreous, autosomal recessive
|
[NCBI]
|
0.001097646
|
|
|
bullous dystrophy, hereditary macular type
|
[NCBI]
|
0.001097646
|
|
|
CVD1
|
[NCBI]
|
0.001097646
|
|
|
IP
|
[NCBI]
|
0.001059722
|
|
|
mental health wellness 1
|
[NCBI]
|
0.00105247
|
|
|
DFN4
|
[NCBI]
|
0.001033783
|
|
|
MYP1
|
[NCBI]
|
0.001033783
|
|
|
TKCR
|
[NCBI]
|
0.001033783
|
|
|
OFD9
|
[NCBI]
|
0.001027808
|
|
|
xx male syndrome
|
[NCBI]
|
0.001019486
|
|
|
MRX3
|
[NCBI]
|
0.000947637
|
|
|
EFMR
|
[NCBI]
|
0.000947637
|
|
|
CTPP1
|
[NCBI]
|
0.000916752
|
|
|
immunoglobulin m, level of
|
[NCBI]
|
0.000910261
|
|
|
pelizaeus-merzbacher-like disease, autosomal recessive, 2
|
[NCBI]
|
0.000891199
|
|
|
EDMD
|
[NCBI]
|
0.000861807
|
|
|
SCAX1
|
[NCBI]
|
0.000853823
|
|
|
spatial visualization, aptitude for
|
[NCBI]
|
0.000849062
|
|
|
CGF1
|
[NCBI]
|
0.000830263
|
|
|
MEAX
|
[NCBI]
|
0.000822934
|
|
|
PHP
|
[NCBI]
|
0.000822934
|
|
|
THAS
|
[NCBI]
|
0.000739229
|
|
|
DFN2
|
[NCBI]
|
0.000739229
|
|
|
SLE
|
[NCBI]
|
0.000737214
|
|
|
hyperglycerolemia
|
[NCBI]
|
0.000723025
|
|
|
HYPX
|
[NCBI]
|
0.000712976
|
|
|
MCOPS7
|
[NCBI]
|
0.000675566
|
|
|
XIST
|
[NCBI]
|
0.000584224
|
|
|
LISX1
|
[NCBI]
|
0.000574151
|
|
|
CF
|
[NCBI]
|
0.000556482
|
|
|
ND
|
[NCBI]
|
0.000506473
|
|
|
nondisjunction
|
[NCBI]
|
0.000498654
|
|
|
ichthyosis, x-linked
|
[NCBI]
|
0.000447494
|
|
|
scleroderma, familial progressive
|
[NCBI]
|
0.00043003
|
|
|
hashimoto thyroiditis
|
[NCBI]
|
0.000403222
|
|
|
OKS
|
[NCBI]
|
0.000402556
|
|
|
HSAS
|
[NCBI]
|
0.000395107
|
|
|
SHOX
|
[NCBI]
|
0.000389675
|
|
|
SGBS1
|
[NCBI]
|
0.000379842
|
|
|
paine syndrome
|
[NCBI]
|
0.000377496
|
|
|
menkes disease
|
[NCBI]
|
0.000364443
|
|
|
PCD
|
[NCBI]
|
0.000344273
|
|
|
h-y antigen receptor
|
[NCBI]
|
0.000341217
|
|
|
muscular dystrophy, hemizygous lethal type
|
[NCBI]
|
0.000339318
|
|
|
GDXY
|
[NCBI]
|
0.000315948
|
|
|
SRA2
|
[NCBI]
|
0.000313455
|
|
|
CDPX1
|
[NCBI]
|
0.000308135
|
|
|
AHC
|
[NCBI]
|
0.000270826
|
|
|
PMD
|
[NCBI]
|
0.000265394
|
|
|
palmoplantar hyperkeratosis with squamous cell carcinoma of skin and sex reversal
|
[NCBI]
|
0.000257258
|
|
|
IL1RAPL1
|
[NCBI]
|
0.0002562679
|
|
|
radioulnar synostosis
|
[NCBI]
|
0.000252272
|
|
|
DKC
|
[NCBI]
|
0.000248686
|
|
|
hermaphroditism, true
|
[NCBI]
|
0.000238035
|
|
|
campomelic dysplasia
|
[NCBI]
|
0.000235858
|
|
|
DAZ
|
[NCBI]
|
0.0002328463
|
|
|
SXI1
|
[NCBI]
|
0.000231853
|
|
|
RS1
|
[NCBI]
|
0.0002298741
|
|
|
FMR1
|
[NCBI]
|
0.0002288739
|
|
|
HMI
|
[NCBI]
|
0.0002264062
|
|
|
XG
|
[NCBI]
|
0.0002258976
|
|
|
spermatogenic failure, nonobstructive, y-linked
|
[NCBI]
|
0.000224553
|
|
|
ALD
|
[NCBI]
|
0.0002203499
|
|
|
hydrocephalus
|
[NCBI]
|
0.0002188655
|
|
|
HTX1
|
[NCBI]
|
0.0002174833
|
|
|
RP2
|
[NCBI]
|
0.0002148443
|
|
|
ISS
|
[NCBI]
|
0.0002071793
|
|
|
DCX
|
[NCBI]
|
0.0002069828
|
|
|
alopecia, congenital
|
[NCBI]
|
0.000204136
|
|
|
neuropathy, hereditary sensory, x-linked
|
[NCBI]
|
0.000204136
|
|
|
leukemia, acute, ?x-linked
|
[NCBI]
|
0.000204136
|
|
|
keratosis follicularis, dwarfism, and cerebral atrophy
|
[NCBI]
|
0.000204136
|
|
|
MRX14
|
[NCBI]
|
0.000204136
|
|
|
omphalocele
|
[NCBI]
|
0.000204136
|
|
|
calvarial hyperostosis
|
[NCBI]
|
0.000204136
|
|
|
spastic paraplegia, optic atrophy, microcephaly, and xy sex reversal
|
[NCBI]
|
0.000204136
|
|
|
AMELX
|
[NCBI]
|
0.0002026685
|
|
|
autism
|
[NCBI]
|
0.0001946444
|
|
|
MTS
|
[NCBI]
|
0.0001944128
|
|
|
CLS
|
[NCBI]
|
0.0001940719
|
|
|
heterotopia, periventricular, x-linked dominant
|
[NCBI]
|
0.0001923689
|
|
|
MAFD1
|
[NCBI]
|
0.0001883017
|
|
|
infantile spasm syndrome, x-linked
|
[NCBI]
|
0.0001871672
|
|
|
XK
|
[NCBI]
|
0.0001870828
|
|
|
AHDS
|
[NCBI]
|
0.0001852507
|
|
|
HEMB
|
[NCBI]
|
0.0001835588
|
|
|
AD
|
[NCBI]
|
0.0001823343
|
|
|
OFD1
|
[NCBI]
|
0.0001684017
|
|
|
CPX
|
[NCBI]
|
0.0001601186
|
|
|
SCZD
|
[NCBI]
|
0.0001589812
|
|
|
CGD
|
[NCBI]
|
0.0001581014
|
|
|
L1CAM
|
[NCBI]
|
0.0001551786
|
|
|
pallister w syndrome
|
[NCBI]
|
0.0001540197
|
|
|
coxoauricular syndrome
|
[NCBI]
|
0.0001540197
|
|
|
spondyloepimetaphyseal dysplasia, x-linked
|
[NCBI]
|
0.0001540197
|
|
|
sjogren-larsson-like ichthyosis without cns or eye involvement
|
[NCBI]
|
0.0001540197
|
|
|
body length, mouse, human homolog
|
[NCBI]
|
0.0001540197
|
|
|
tooth size
|
[NCBI]
|
0.0001540197
|
|
|
MCOPCT3
|
[NCBI]
|
0.0001540197
|
|
|
CSF2RA
|
[NCBI]
|
0.0001528443
|
|
|
POF1
|
[NCBI]
|
0.0001518098
|
|
|
JARID1D
|
[NCBI]
|
0.0001480318
|
|
|
KAL1
|
[NCBI]
|
0.0001470147
|
|
|
RPS4X
|
[NCBI]
|
0.0001459444
|
|
|
PHKA1
|
[NCBI]
|
0.0001459444
|
|
|
ichthyosis hystrix gravior
|
[NCBI]
|
0.0001455892
|
|
|
DMD
|
[NCBI]
|
0.0001444792
|
|
|
breasts and nipples, absence of
|
[NCBI]
|
0.0001436155
|
|
|
CRC
|
[NCBI]
|
0.0001403182
|
|
|
myotubular myopathy with abnormal genital development
|
[NCBI]
|
0.000135185
|
|
|
MRX63
|
[NCBI]
|
0.000135185
|
|
|
genitopalatocardiac syndrome
|
[NCBI]
|
0.000135185
|
|
|
pterygium syndrome, multiple, x-linked
|
[NCBI]
|
0.000135185
|
|
|
XLP1
|
[NCBI]
|
0.0001322432
|
|
|
mental health wellness 2
|
[NCBI]
|
0.0001246723
|
|
|
pseudohermaphroditism, incomplete male, type i
|
[NCBI]
|
0.0001157426
|
|
|
POF2A
|
[NCBI]
|
0.0001139717
|
|
|
MRX21
|
[NCBI]
|
0.0001139717
|
|
|
DSS
|
[NCBI]
|
0.0001107851
|
|
|
hypogammaglobulinemia and isolated growth hormone deficiency, x-linked
|
[NCBI]
|
0.0001107593
|
|
|
muscle glycogenosis, x-linked
|
[NCBI]
|
0.0001107593
|
|
|
IL2RG
|
[NCBI]
|
0.0001095373
|
|
|
HPRT1
|
[NCBI]
|
0.0001087992
|
|
|
KLHL4
|
[NCBI]
|
0.0001085803
|
|
|
neural tube defects, x-linked
|
[NCBI]
|
0.0001068042
|
|
|
ED1
|
[NCBI]
|
0.0001058012
|
|
|
CHM
|
[NCBI]
|
0.0001051165
|
|
|
MTM1
|
[NCBI]
|
0.0001047031
|
|
|
SMAX1
|
[NCBI]
|
0.0001037272
|
|
|
LNS
|
[NCBI]
|
0.0001030159
|
|
|
ARX
|
[NCBI]
|
0.0001016607
|
|
|
amme complex
|
[NCBI]
|
0.0001008655
|
|
|
IL1RAPL2
|
[NCBI]
|
0.0001003373
|
|
|
wildervanck syndrome
|
[NCBI]
|
9.90949e-05
|
|
|
vacterl association with hydrocephalus
|
[NCBI]
|
9.85934e-05
|
|
|
HYR
|
[NCBI]
|
9.80725e-05
|
|
|
glycogen storage disease ixa
|
[NCBI]
|
9.78985e-05
|
|
|
suppressor of variegation 3-9, drosophila, homolog of, 2
|
[NCBI]
|
9.72289e-05
|
|
|
MRX9
|
[NCBI]
|
9.58004e-05
|
|
|
PHEX
|
[NCBI]
|
9.50137e-05
|
|
|
NR0B1
|
[NCBI]
|
9.46805e-05
|
|
|
NDP
|
[NCBI]
|
9.44501e-05
|
|
|
vacterl association with hydrocephalus, x-linked
|
[NCBI]
|
9.38204e-05
|
|
|
MEA1
|
[NCBI]
|
9.37134e-05
|
|
|
OA1
|
[NCBI]
|
9.31749e-05
|
|
|
AIS
|
[NCBI]
|
9.18796e-05
|
|
|
FLNA
|
[NCBI]
|
8.94819e-05
|
|
|
NYS1
|
[NCBI]
|
8.92366e-05
|
|
|
congenital hemidysplasia with ichthyosiform erythroderma and limb defects
|
[NCBI]
|
8.65735e-05
|
|
|
ZFP37
|
[NCBI]
|
8.65695e-05
|
|
|
MRX49
|
[NCBI]
|
8.65695e-05
|
|
|
pseudotrisomy 13 syndrome
|
[NCBI]
|
8.59112e-05
|
|
|
ASMTL
|
[NCBI]
|
8.34611e-05
|
|
|
PPEF1
|
[NCBI]
|
8.34611e-05
|
|
|
sertoli cell-only syndrome, y-linked
|
[NCBI]
|
8.22384e-05
|
|
|
GUCY2F
|
[NCBI]
|
8.14442e-05
|
|
|
MRXS13
|
[NCBI]
|
8.08143e-05
|
|
|
G6PD
|
[NCBI]
|
8.00863e-05
|
|
|
feingold syndrome
|
[NCBI]
|
7.89546e-05
|
|
|
ichthyosis vulgaris
|
[NCBI]
|
7.89546e-05
|
|
|
MIC2Y
|
[NCBI]
|
7.87522e-05
|
|
|
HHS
|
[NCBI]
|
7.83169e-05
|
|
|
IDH3G
|
[NCBI]
|
7.82726e-05
|
|
|
cyclic hematopoiesis
|
[NCBI]
|
7.79209e-05
|
|
|
RENBP
|
[NCBI]
|
7.77607e-05
|
|
|
OPD1
|
[NCBI]
|
7.56171e-05
|
|
|
multiple pterygium syndrome, escobar variant
|
[NCBI]
|
7.56171e-05
|
|
|
amelogenesis imperfecta, hypoplastic/hypomaturation, x-linked 1
|
[NCBI]
|
7.56171e-05
|
|
|
denys-drash syndrome
|
[NCBI]
|
7.45872e-05
|
|
|
NCIE1
|
[NCBI]
|
7.45872e-05
|
|
|
RP
|
[NCBI]
|
7.43362e-05
|
|
|
CXORF6
|
[NCBI]
|
7.28908e-05
|
|
|
properdin deficiency, x-linked
|
[NCBI]
|
7.15717e-05
|
|
|
VCX3A
|
[NCBI]
|
7.13922e-05
|
|
|
SUV39H1
|
[NCBI]
|
7.0983e-05
|
|
|
TSPY
|
[NCBI]
|
7.03252e-05
|
|
|
CCT
|
[NCBI]
|
6.88934e-05
|
|
|
EEC3
|
[NCBI]
|
6.83761e-05
|
|
|
ichthyosis congenita, harlequin fetus type
|
[NCBI]
|
6.74949e-05
|
|
|
DIAPH2
|
[NCBI]
|
6.67085e-05
|
|
|
IPEX
|
[NCBI]
|
6.62372e-05
|
|
|
SPG2
|
[NCBI]
|
6.50631e-05
|
|
|
AFD1
|
[NCBI]
|
6.48311e-05
|
|
|
NSDHL
|
[NCBI]
|
6.47199e-05
|
|
|
GJB1
|
[NCBI]
|
6.3776e-05
|
|
|
CD99
|
[NCBI]
|
6.37065e-05
|
|
|
BFLS
|
[NCBI]
|
6.36873e-05
|
|
|
mucopolysaccharidosis type ii
|
[NCBI]
|
6.30999e-05
|
|
|
FANCB
|
[NCBI]
|
6.30683e-05
|
|
|
NHS
|
[NCBI]
|
6.30683e-05
|
|
|
CBAVD
|
[NCBI]
|
6.29281e-05
|
|
|
MNS
|
[NCBI]
|
6.25567e-05
|
|
|
masa syndrome
|
[NCBI]
|
6.19521e-05
|
|
|
NHS
|
[NCBI]
|
6.17881e-05
|
|
|
MTRR
|
[NCBI]
|
6.00671e-05
|
|
|
FACL4
|
[NCBI]
|
5.8818e-05
|
|
|
MCF2
|
[NCBI]
|
5.87479e-05
|
|
|
deafness, conductive, with stapes fixation
|
[NCBI]
|
5.87473e-05
|
|
|
ZIC3
|
[NCBI]
|
5.59543e-05
|
|
|
POU3F4
|
[NCBI]
|
5.59543e-05
|
|
|
TIMM8A
|
[NCBI]
|
5.49715e-05
|
|
|
MRXHF1
|
[NCBI]
|
5.44924e-05
|
|
|
GDI1
|
[NCBI]
|
5.4251e-05
|
|
|
faciogenital dysplasia
|
[NCBI]
|
5.42284e-05
|
|
|
LAMR1
|
[NCBI]
|
5.40263e-05
|
|
|
ACTA1
|
[NCBI]
|
5.31571e-05
|
|
|
PFC
|
[NCBI]
|
5.23214e-05
|
|
|
OCRL
|
[NCBI]
|
5.04818e-05
|
|
|
PPSH
|
[NCBI]
|
4.92987e-05
|
|
|
H2AFX
|
[NCBI]
|
4.90158e-05
|
|
|
CBP
|
[NCBI]
|
4.83655e-05
|
|
|
hemophilia a
|
[NCBI]
|
4.77864e-05
|
|
|
EBP
|
[NCBI]
|
4.72193e-05
|
|
|
FPLD2
|
[NCBI]
|
4.65662e-05
|
|
|
FDH
|
[NCBI]
|
4.64468e-05
|
|
|
DKC1
|
[NCBI]
|
4.49884e-05
|
|
|
EDA
|
[NCBI]
|
4.44909e-05
|
|
|
GK
|
[NCBI]
|
4.40975e-05
|
|
|
CDPX2
|
[NCBI]
|
4.31773e-05
|
|
|
SMA3
|
[NCBI]
|
4.30824e-05
|
|
|
CMTX1
|
[NCBI]
|
4.30824e-05
|
|
|
CHM
|
[NCBI]
|
4.20142e-05
|
|
|
homocystinuria due to deficiency of n(5,10)-methylenetetrahydrofolate reductase activity
|
[NCBI]
|
4.17434e-05
|
|
|
CBX5
|
[NCBI]
|
4.147563e-05
|
|
|
MTM1
|
[NCBI]
|
4.10744e-05
|
|
|
TP73L
|
[NCBI]
|
4.10107e-05
|
|
|
RPS6KA3
|
[NCBI]
|
4.02152e-05
|
|
|
CYBB
|
[NCBI]
|
3.88443e-05
|
|
|
BTHS
|
[NCBI]
|
3.88124e-05
|
|
|
GPC3
|
[NCBI]
|
3.87234e-05
|
|
|
OTC
|
[NCBI]
|
3.8723e-05
|
|
|
IKBKG
|
[NCBI]
|
3.86789e-05
|
|
|
RB1
|
[NCBI]
|
3.83672e-05
|
|
|
SOX9
|
[NCBI]
|
3.75909e-05
|
|
|
BMD
|
[NCBI]
|
3.70294e-05
|
|
|
PIGA
|
[NCBI]
|
3.66967e-05
|
|
|
AR
|
[NCBI]
|
3.54342e-05
|
|
|
thyroid carcinoma, papillary
|
[NCBI]
|
3.39606e-05
|
|
|
F13A1
|
[NCBI]
|
3.32199e-05
|
|
|
FOXP3
|
[NCBI]
|
3.00622e-05
|
|
|
BPES
|
[NCBI]
|
2.94974e-05
|
|
|
bullous erythroderma ichthyosiformis congenita of brocq
|
[NCBI]
|
2.89107e-05
|
|
|
MAOA
|
[NCBI]
|
2.705214e-05
|
|
|
ABCD1
|
[NCBI]
|
2.70272e-05
|
|
|
ornithine transcarbamylase deficiency, hyperammonemia due to
|
[NCBI]
|
2.67488e-05
|
|
|
BTK
|
[NCBI]
|
2.2153e-05
|
|
|
PRL
|
[NCBI]
|
2.196826e-05
|
|
|
hypogonadotropic hypogonadism
|
[NCBI]
|
2.156854e-05
|
|
|
alopecia, androgenetic
|
[NCBI]
|
1.964442e-05
|
|
|
RHO
|
[NCBI]
|
1.957396e-05
|
|
|
NS1
|
[NCBI]
|
1.776233e-05
|
|
|
DNMT1
|
[NCBI]
|
1.761138e-05
|
|
|
MECP2
|
[NCBI]
|
1.687436e-05
|
|
|
GHR
|
[NCBI]
|
1.439288e-05
|
|
|
fabry disease
|
[NCBI]
|
1.356817e-05
|
|
|
WAS
|
[NCBI]
|
1.336524e-05
|
|
|
MB
|
[NCBI]
|
1.228871e-05
|
|
|
DMD
|
[NCBI]
|
1.217261e-05
|
|
|
AFP
|
[NCBI]
|
7.56572e-06
|
|
|
TYMS
|
[NCBI]
|
6.94386e-06
|
|
|
PWS
|
[NCBI]
|
3.099065e-06
|
|
|
PJS
|
[NCBI]
|
2.66418e-06
|
|
|
CFTR
|
[NCBI]
|
1.40489e-06
|
|
|
AS
|
[NCBI]
|
6.475248e-07
|
|
|
VDR
|
[NCBI]
|
1.773148e-08
|
|