|
OMIM |
Link |
Information gain |
01 |
|
thrombocytopenia-absent radius syndrome
|
[NCBI]
|
0.021677
|
|
|
thrombocytopenic purpura, autoimmune
|
[NCBI]
|
0.00398061
|
|
|
PF4
|
[NCBI]
|
0.00300268
|
|
|
thrombasthenia-thrombocytopenia, hereditary
|
[NCBI]
|
0.00256974
|
|
|
WAS
|
[NCBI]
|
0.00192542
|
|
|
GPS
|
[NCBI]
|
0.00159882
|
|
|
THC2
|
[NCBI]
|
0.00134605
|
|
|
MHA
|
[NCBI]
|
0.00129069
|
|
|
SLE
|
[NCBI]
|
0.000990009
|
|
|
FTNS
|
[NCBI]
|
0.000951474
|
|
|
MYH9
|
[NCBI]
|
0.000912361
|
|
|
SBS
|
[NCBI]
|
0.000910426
|
|
|
hemangioma-thrombocytopenia syndrome
|
[NCBI]
|
0.000882438
|
|
|
giant platelet syndrome
|
[NCBI]
|
0.000775172
|
|
|
THC1
|
[NCBI]
|
0.000713962
|
|
|
CF
|
[NCBI]
|
0.000580277
|
|
|
epstein syndrome
|
[NCBI]
|
0.000557578
|
|
|
dianzani autoimmune lymphoproliferative disease
|
[NCBI]
|
0.000553779
|
|
|
RA
|
[NCBI]
|
0.000530114
|
|
|
GHDD
|
[NCBI]
|
0.000501042
|
|
|
WAS
|
[NCBI]
|
0.000493094
|
|
|
TTP
|
[NCBI]
|
0.000474424
|
|
|
eosinophilia, familial
|
[NCBI]
|
0.000462003
|
|
|
thrombocytopenia, autosomal recessive
|
[NCBI]
|
0.000462003
|
|
|
THPO
|
[NCBI]
|
0.000387602
|
|
|
MPL
|
[NCBI]
|
0.000376272
|
|
|
visceral neuropathy, familial, autosomal recessive
|
[NCBI]
|
0.000364525
|
|
|
dyserythropoietic anemia with thrombocytopenia
|
[NCBI]
|
0.000330646
|
|
|
CAMT
|
[NCBI]
|
0.000330646
|
|
|
klippel-trenaunay-weber syndrome
|
[NCBI]
|
0.000308379
|
|
|
GATA1
|
[NCBI]
|
0.000252811
|
|
|
bernard-soulier syndrome, benign autosomal dominant
|
[NCBI]
|
0.00024794
|
|
|
thrombocytopenia, platelet dysfunction, hemolysis, and imbalanced globin synthesis
|
[NCBI]
|
0.00024794
|
|
|
ALPS
|
[NCBI]
|
0.000211622
|
|
|
ITGA2
|
[NCBI]
|
0.000200618
|
|
|
platelet disorder, familial, with associated myeloid malignancy
|
[NCBI]
|
0.000193589
|
|
|
TCPT
|
[NCBI]
|
0.000193589
|
|
|
aHUS
|
[NCBI]
|
0.000190248
|
|
|
platelet glycoprotein iv deficiency
|
[NCBI]
|
0.000170844
|
|
|
radioulnar synostosis with amegakaryocytic thrombocytopenia
|
[NCBI]
|
0.000165264
|
|
|
hemophagocytic lymphohistiocytosis, familial, 1
|
[NCBI]
|
0.000131848
|
|
|
ITGB3
|
[NCBI]
|
0.000128033
|
|
|
MASTL
|
[NCBI]
|
0.000127754
|
|
|
ivic syndrome
|
[NCBI]
|
0.000120517
|
|
|
TPMT
|
[NCBI]
|
0.000119512
|
|
|
ZFPM1
|
[NCBI]
|
0.000108788
|
|
|
ADAMTS13
|
[NCBI]
|
0.000106368
|
|
|
MG
|
[NCBI]
|
0.00010283
|
|
|
EPO
|
[NCBI]
|
0.000100221
|
|
|
intestinal pseudoobstruction, neuronal, chronic idiopathic, x-linked
|
[NCBI]
|
9.29327e-05
|
|
|
CD36
|
[NCBI]
|
9.13231e-05
|
|
|
RUNX1
|
[NCBI]
|
8.63635e-05
|
|
|
myeloproliferative disease, autosomal recessive
|
[NCBI]
|
8.26171e-05
|
|
|
spastic paraplegia and evans syndrome
|
[NCBI]
|
8.26171e-05
|
|
|
macrothrombocytopenia and progressive sensorineural deafness
|
[NCBI]
|
8.26171e-05
|
|
|
CDG2F
|
[NCBI]
|
8.26171e-05
|
|
|
osteochondrodysplasia, rhizomelic, with callosal agenesis, thrombocytopenia, hydrocephalus, and hypertension
|
[NCBI]
|
8.26171e-05
|
|
|
stormorken syndrome
|
[NCBI]
|
8.26171e-05
|
|
|
giant platelet syndrome with thrombocytopenia
|
[NCBI]
|
8.26171e-05
|
|
|
IN
|
[NCBI]
|
8.26171e-05
|
|
|
thrombocytopenia with elevated serum iga and renal disease
|
[NCBI]
|
8.26171e-05
|
|
|
platelet disorder, undefined
|
[NCBI]
|
8.26171e-05
|
|
|
von willebrand disease
|
[NCBI]
|
8.19272e-05
|
|
|
antiphospholipid syndrome
|
[NCBI]
|
7.86095e-05
|
|
|
FLI1
|
[NCBI]
|
7.60522e-05
|
|
|
HHS
|
[NCBI]
|
7.33791e-05
|
|
|
GP1BA
|
[NCBI]
|
6.55931e-05
|
|
|
CXCL12
|
[NCBI]
|
6.44715e-05
|
|
|
MYH10
|
[NCBI]
|
6.38558e-05
|
|
|
JBS
|
[NCBI]
|
6.33094e-05
|
|
|
revesz syndrome
|
[NCBI]
|
6.02438e-05
|
|
|
glanzmann thrombasthenia, autosomal dominant
|
[NCBI]
|
6.02438e-05
|
|
|
thrombocytopenia, cyclic
|
[NCBI]
|
6.02438e-05
|
|
|
IFRD1
|
[NCBI]
|
5.00912e-05
|
|
|
HOXA11
|
[NCBI]
|
5.00912e-05
|
|
|
HPA-2
|
[NCBI]
|
5.00912e-05
|
|
|
C1GALT1
|
[NCBI]
|
5.00912e-05
|
|
|
HTR2B
|
[NCBI]
|
4.49059e-05
|
|
|
RPS14
|
[NCBI]
|
4.49059e-05
|
|
|
PECAM1
|
[NCBI]
|
4.49059e-05
|
|
|
thrombasthenia of glanzmann and naegeli
|
[NCBI]
|
4.33414e-05
|
|
|
SDS
|
[NCBI]
|
4.28941e-05
|
|
|
PD
|
[NCBI]
|
4.17007e-05
|
|
|
RABGGTA
|
[NCBI]
|
4.15441e-05
|
|
|
ATOX1
|
[NCBI]
|
4.15441e-05
|
|
|
NFE2
|
[NCBI]
|
4.15441e-05
|
|
|
DKC
|
[NCBI]
|
4.03126e-05
|
|
|
mevalonic aciduria
|
[NCBI]
|
3.92909e-05
|
|
|
CCNC
|
[NCBI]
|
3.90485e-05
|
|
|
CEACAM5
|
[NCBI]
|
3.76125e-05
|
|
|
IFNA2
|
[NCBI]
|
3.7063e-05
|
|
|
TPH1
|
[NCBI]
|
3.7063e-05
|
|
|
congenital disorder of glycosylation, type i/iix
|
[NCBI]
|
3.66758e-05
|
|
|
FHL2
|
[NCBI]
|
3.66758e-05
|
|
|
PTH
|
[NCBI]
|
3.47329e-05
|
|
|
radioulnar synostosis
|
[NCBI]
|
3.44515e-05
|
|
|
F3
|
[NCBI]
|
3.41554e-05
|
|
|
HTR2A
|
[NCBI]
|
3.2776e-05
|
|
|
JAK2
|
[NCBI]
|
3.26244e-05
|
|
|
HPS2
|
[NCBI]
|
3.25193e-05
|
|
|
TNF
|
[NCBI]
|
3.12663e-05
|
|
|
VEGF
|
[NCBI]
|
3.01449e-05
|
|
|
sea-blue histiocyte disease
|
[NCBI]
|
2.92894e-05
|
|
|
thiopurine s-methyltransferase deficiency
|
[NCBI]
|
2.92894e-05
|
|
|
PTTG1
|
[NCBI]
|
2.90036e-05
|
|
|
AP3B1
|
[NCBI]
|
2.90036e-05
|
|
|
RP
|
[NCBI]
|
2.85155e-05
|
|
|
von willebrand disease, recessive form
|
[NCBI]
|
2.79131e-05
|
|
|
CD
|
[NCBI]
|
2.78299e-05
|
|
|
IFNA1
|
[NCBI]
|
2.72263e-05
|
|
|
CXCR4
|
[NCBI]
|
2.6307e-05
|
|
|
TNFRSF1B
|
[NCBI]
|
2.33198e-05
|
|
|
ACADS
|
[NCBI]
|
2.29036e-05
|
|
|
KLK3
|
[NCBI]
|
2.28827e-05
|
|
|
pearson marrow-pancreas syndrome
|
[NCBI]
|
2.25552e-05
|
|
|
PMM2
|
[NCBI]
|
2.25054e-05
|
|
|
TFPI
|
[NCBI]
|
2.23602e-05
|
|
|
cirrhosis, familial
|
[NCBI]
|
2.17005e-05
|
|
|
factor xii deficiency
|
[NCBI]
|
2.17005e-05
|
|
|
immunoosseous dysplasia, schimke type
|
[NCBI]
|
2.08989e-05
|
|
|
TRMA
|
[NCBI]
|
2.08989e-05
|
|
|
DPYD
|
[NCBI]
|
1.98251e-05
|
|
|
IPEX
|
[NCBI]
|
1.94333e-05
|
|
|
TNFRSF6
|
[NCBI]
|
1.92636e-05
|
|
|
neuraminidase deficiency with beta-galactosidase deficiency
|
[NCBI]
|
1.73193e-05
|
|
|
NS1
|
[NCBI]
|
1.65276e-05
|
|
|
CSF3
|
[NCBI]
|
1.62942e-05
|
|
|
FOXP3
|
[NCBI]
|
1.61032e-05
|
|
|
OPTB1
|
[NCBI]
|
1.53665e-05
|
|
|
LIPC
|
[NCBI]
|
1.52084e-05
|
|
|
IL2
|
[NCBI]
|
1.3464e-05
|
|
|
tyrosinemia, type i
|
[NCBI]
|
1.32555e-05
|
|
|
CDLS1
|
[NCBI]
|
1.26152e-05
|
|
|
CLL
|
[NCBI]
|
1.20222e-05
|
|
|
RBS
|
[NCBI]
|
1.13325e-05
|
|
|
APOE
|
[NCBI]
|
1.02439e-05
|
|
|
KDR
|
[NCBI]
|
9.2964e-06
|
|
|
BCHE
|
[NCBI]
|
8.77063e-06
|
|
|
CDG1A
|
[NCBI]
|
8.25646e-06
|
|
|
PCNA
|
[NCBI]
|
7.70385e-06
|
|
|
TYMS
|
[NCBI]
|
7.69061e-06
|
|
|
lymphoma, non-hodgkin, familial
|
[NCBI]
|
6.99145e-06
|
|
|
OSM
|
[NCBI]
|
5.83206e-06
|
|
|
HEMB
|
[NCBI]
|
5.32568e-06
|
|
|
AFP
|
[NCBI]
|
5.17861e-06
|
|
|
MPO
|
[NCBI]
|
4.6286e-06
|
|
|
ACHE
|
[NCBI]
|
1.74162e-06
|
|
|
CNTF
|
[NCBI]
|
1.54752e-06
|
|
|
G6PD
|
[NCBI]
|
1.40124e-06
|
|
|
SLOS
|
[NCBI]
|
8.29485e-07
|
|
|
XDH
|
[NCBI]
|
7.28663e-07
|
|
|
ACH
|
[NCBI]
|
6.66301e-07
|
|
|
BBS
|
[NCBI]
|
4.47663e-07
|
|
|
VHL
|
[NCBI]
|
4.20553e-07
|
|
|
CHS
|
[NCBI]
|
3.7826e-07
|
|
|
DHFR
|
[NCBI]
|
2.03752e-07
|
|
|
CAT
|
[NCBI]
|
4.54543e-08
|
|
|
HPS
|
[NCBI]
|
2.75358e-08
|
|
|
PCD
|
[NCBI]
|
1.33994e-08
|
|
|
LPL
|
[NCBI]
|
7.32218e-09
|
|
|
HBB
|
[NCBI]
|
3.26685e-10
|
|