|
OMIM |
Link |
Information gain |
01 |
|
SLE
|
[NCBI]
|
0.00394407
|
|
|
neutrophilic dermatosis, acute febrile
|
[NCBI]
|
0.00260033
|
|
|
carnitine deficiency, myopathic
|
[NCBI]
|
0.00241196
|
|
|
enteropathy, protein-losing
|
[NCBI]
|
0.00213118
|
|
|
temporal arteritis
|
[NCBI]
|
0.00187288
|
|
|
thrombocytopenic purpura, autoimmune
|
[NCBI]
|
0.00176334
|
|
|
GPS
|
[NCBI]
|
0.00175138
|
|
|
transient erythroblastopenia of childhood
|
[NCBI]
|
0.00160918
|
|
|
thrombasthenia-thrombocytopenia, hereditary
|
[NCBI]
|
0.00160918
|
|
|
lymphoma, non-hodgkin, familial
|
[NCBI]
|
0.00130075
|
|
|
neutropenia, chronic familial
|
[NCBI]
|
0.00128598
|
|
|
MG
|
[NCBI]
|
0.000735073
|
|
|
hemophagocytic lymphohistiocytosis, familial, 1
|
[NCBI]
|
0.000695279
|
|
|
CF
|
[NCBI]
|
0.000607866
|
|
|
SPS
|
[NCBI]
|
0.000392717
|
|
|
apnea, obstructive sleep
|
[NCBI]
|
0.000240833
|
|
|
anemia, autoimmune hemolytic
|
[NCBI]
|
0.000142954
|
|
|
LGMD2M
|
[NCBI]
|
0.000102801
|
|
|
asthma, short stature, and elevated iga
|
[NCBI]
|
0.000102801
|
|
|
granulocytopenia with immunoglobulin abnormality
|
[NCBI]
|
0.000102801
|
|
|
histiocytic dermatoarthritis
|
[NCBI]
|
0.000102801
|
|
|
DBA
|
[NCBI]
|
0.000101009
|
|
|
GRTH
|
[NCBI]
|
9.87529e-05
|
|
|
RNASE3
|
[NCBI]
|
9.2465e-05
|
|
|
HNA
|
[NCBI]
|
8.49363e-05
|
|
|
PTH
|
[NCBI]
|
8.0975e-05
|
|
|
BGLAP
|
[NCBI]
|
7.83012e-05
|
|
|
KLK3
|
[NCBI]
|
7.62536e-05
|
|
|
camurati-engelmann disease
|
[NCBI]
|
7.46747e-05
|
|
|
mitochondrial myopathy with lactic acidosis
|
[NCBI]
|
7.14611e-05
|
|
|
satoyoshi syndrome
|
[NCBI]
|
7.14611e-05
|
|
|
SRN1
|
[NCBI]
|
5.97888e-05
|
|
|
HIDS
|
[NCBI]
|
5.42858e-05
|
|
|
BFH
|
[NCBI]
|
5.2297e-05
|
|
|
hla-d histocompatibility type
|
[NCBI]
|
4.99925e-05
|
|
|
rheumatoid arthritis, systemic juvenile
|
[NCBI]
|
4.67906e-05
|
|
|
CINCA
|
[NCBI]
|
4.67906e-05
|
|
|
IFNA1
|
[NCBI]
|
4.2646e-05
|
|
|
mevalonic aciduria
|
[NCBI]
|
4.24537e-05
|
|
|
hypercalcemia, idiopathic, of infancy
|
[NCBI]
|
3.88895e-05
|
|
|
ALK
|
[NCBI]
|
3.60136e-05
|
|
|
mitochondrial myopathy with diabetes
|
[NCBI]
|
3.58744e-05
|
|
|
TINU
|
[NCBI]
|
3.58744e-05
|
|
|
pemphigus vulgaris, familial
|
[NCBI]
|
3.327e-05
|
|
|
FA
|
[NCBI]
|
3.28037e-05
|
|
|
sarcoidosis
|
[NCBI]
|
3.09844e-05
|
|
|
THC2
|
[NCBI]
|
2.89533e-05
|
|
|
CVID
|
[NCBI]
|
2.82121e-05
|
|
|
infantile spasm syndrome, x-linked
|
[NCBI]
|
2.71304e-05
|
|
|
chromosome 5q deletion syndrome
|
[NCBI]
|
2.71304e-05
|
|
|
autoimmune disease
|
[NCBI]
|
2.71304e-05
|
|
|
EFE
|
[NCBI]
|
2.71304e-05
|
|
|
ICP
|
[NCBI]
|
2.71304e-05
|
|
|
CD226
|
[NCBI]
|
2.68301e-05
|
|
|
NPM1
|
[NCBI]
|
2.60841e-05
|
|
|
IFNA2
|
[NCBI]
|
2.57548e-05
|
|
|
synovitis, granulomatous, with uveitis and cranial neuropathies
|
[NCBI]
|
2.54808e-05
|
|
|
hemangioma-thrombocytopenia syndrome
|
[NCBI]
|
2.54808e-05
|
|
|
NPHS1
|
[NCBI]
|
2.54808e-05
|
|
|
von willebrand disease
|
[NCBI]
|
2.49612e-05
|
|
|
MTTF
|
[NCBI]
|
2.4861e-05
|
|
|
LAG5
|
[NCBI]
|
2.34281e-05
|
|
|
IGFALS
|
[NCBI]
|
2.34193e-05
|
|
|
ZNF198
|
[NCBI]
|
2.28348e-05
|
|
|
FKTN
|
[NCBI]
|
2.23014e-05
|
|
|
SEPT9
|
[NCBI]
|
2.18168e-05
|
|
|
myasthenic syndrome, congenital, associated with episodic apnea
|
[NCBI]
|
2.13315e-05
|
|
|
adrenal hyperplasia, congenital, due to 21-hydroxylase deficiency
|
[NCBI]
|
2.10675e-05
|
|
|
GRA
|
[NCBI]
|
2.03875e-05
|
|
|
OPTB1
|
[NCBI]
|
1.90683e-05
|
|
|
SCCMS
|
[NCBI]
|
1.90683e-05
|
|
|
EGF
|
[NCBI]
|
1.8439e-05
|
|
|
DKC
|
[NCBI]
|
1.80533e-05
|
|
|
SEDC
|
[NCBI]
|
1.80533e-05
|
|
|
BIRC5
|
[NCBI]
|
1.78034e-05
|
|
|
CYP11B1
|
[NCBI]
|
1.71935e-05
|
|
|
adrenal hyperplasia, congenital, due to 17-alpha-hydroxylase deficiency
|
[NCBI]
|
1.7105e-05
|
|
|
BL
|
[NCBI]
|
1.6908e-05
|
|
|
MVK
|
[NCBI]
|
1.66478e-05
|
|
|
RMD
|
[NCBI]
|
1.62167e-05
|
|
|
adrenal hyperplasia, congenital, due to steroid 11-beta-hydroxylase deficiency
|
[NCBI]
|
1.62167e-05
|
|
|
CGL2
|
[NCBI]
|
1.62167e-05
|
|
|
CRMO
|
[NCBI]
|
1.53828e-05
|
|
|
MBP
|
[NCBI]
|
1.50542e-05
|
|
|
complement component 2 deficiency
|
[NCBI]
|
1.49061e-05
|
|
|
TNFRSF1B
|
[NCBI]
|
1.49061e-05
|
|
|
DSG1
|
[NCBI]
|
1.45496e-05
|
|
|
ERBB2
|
[NCBI]
|
1.41101e-05
|
|
|
TFRC
|
[NCBI]
|
1.33312e-05
|
|
|
ABCC1
|
[NCBI]
|
1.27507e-05
|
|
|
tyrosinemia, type i
|
[NCBI]
|
1.25788e-05
|
|
|
TNF
|
[NCBI]
|
1.25277e-05
|
|
|
DSG3
|
[NCBI]
|
1.25018e-05
|
|
|
megaloblastic anemia 1
|
[NCBI]
|
1.25005e-05
|
|
|
THPO
|
[NCBI]
|
1.19254e-05
|
|
|
ANG
|
[NCBI]
|
1.17912e-05
|
|
|
VCP
|
[NCBI]
|
1.16606e-05
|
|
|
B2M
|
[NCBI]
|
1.16606e-05
|
|
|
COL2A1
|
[NCBI]
|
1.11126e-05
|
|
|
LKS
|
[NCBI]
|
1.07206e-05
|
|
|
IL2
|
[NCBI]
|
1.00775e-05
|
|
|
WFS1
|
[NCBI]
|
9.67823e-06
|
|
|
TPMT
|
[NCBI]
|
9.35032e-06
|
|
|
hypophosphatasia, infantile
|
[NCBI]
|
9.19467e-06
|
|
|
EPO
|
[NCBI]
|
9.07491e-06
|
|
|
FGFR1
|
[NCBI]
|
9.0428e-06
|
|
|
RNASE2
|
[NCBI]
|
9.0428e-06
|
|
|
hemophilia a
|
[NCBI]
|
7.84099e-06
|
|
|
TNFRSF11B
|
[NCBI]
|
7.15451e-06
|
|
|
periodic fever, familial, autosomal dominant
|
[NCBI]
|
7.09561e-06
|
|
|
HHC1
|
[NCBI]
|
6.73134e-06
|
|
|
DCK
|
[NCBI]
|
6.48392e-06
|
|
|
BCPM
|
[NCBI]
|
6.38328e-06
|
|
|
PLG
|
[NCBI]
|
5.8877e-06
|
|
|
SHBG
|
[NCBI]
|
5.68675e-06
|
|
|
GHR
|
[NCBI]
|
5.41686e-06
|
|
|
RA
|
[NCBI]
|
4.9447e-06
|
|
|
NPY
|
[NCBI]
|
4.02342e-06
|
|
|
MAG
|
[NCBI]
|
3.1672e-06
|
|
|
ACHE
|
[NCBI]
|
2.97788e-06
|
|
|
HP
|
[NCBI]
|
2.70392e-06
|
|
|
DMD
|
[NCBI]
|
2.57708e-06
|
|
|
AVP
|
[NCBI]
|
2.54372e-06
|
|
|
CHS
|
[NCBI]
|
2.48774e-06
|
|
|
MPO
|
[NCBI]
|
2.39694e-06
|
|
|
PRL
|
[NCBI]
|
2.24607e-06
|
|
|
PCNA
|
[NCBI]
|
1.83686e-06
|
|
|
FRAP1
|
[NCBI]
|
1.59457e-06
|
|
|
OCP
|
[NCBI]
|
1.49968e-06
|
|
|
PTHLH
|
[NCBI]
|
1.44984e-06
|
|
|
TTR
|
[NCBI]
|
1.31987e-06
|
|
|
KSS
|
[NCBI]
|
7.96109e-07
|
|
|
SPP1
|
[NCBI]
|
7.74815e-07
|
|
|
VEGF
|
[NCBI]
|
7.25312e-07
|
|
|
HGF
|
[NCBI]
|
5.34043e-07
|
|
|
AR
|
[NCBI]
|
5.26441e-07
|
|
|
CEACAM5
|
[NCBI]
|
1.89949e-07
|
|
|
fabry disease
|
[NCBI]
|
1.85807e-07
|
|
|
VDR
|
[NCBI]
|
1.40275e-07
|
|
|
ALPS
|
[NCBI]
|
1.06871e-07
|
|
|
wilson disease
|
[NCBI]
|
2.20913e-08
|
|
|
VIP
|
[NCBI]
|
1.43092e-08
|
|
|
FMF
|
[NCBI]
|
1.31241e-08
|
|
|
CRH
|
[NCBI]
|
6.15563e-11
|
|