|
OMIM |
Link |
Information gain |
01 |
|
hemophagocytic lymphohistiocytosis, familial, 1
|
[NCBI]
|
0.00567286
|
|
|
behcet syndrome
|
[NCBI]
|
0.00152527
|
|
|
sea-blue histiocyte disease
|
[NCBI]
|
0.00141944
|
|
|
histiocytosis with joint contractures and sensorineural deafness
|
[NCBI]
|
0.00112909
|
|
|
panbronchiolitis, diffuse
|
[NCBI]
|
0.000936179
|
|
|
NPC1
|
[NCBI]
|
0.000610628
|
|
|
CDAN2
|
[NCBI]
|
0.000567166
|
|
|
cardiomyopathy, infantile histiocytoid
|
[NCBI]
|
0.000463633
|
|
|
niemann-pick disease, type b
|
[NCBI]
|
0.000347054
|
|
|
neutrophilia, hereditary
|
[NCBI]
|
0.000193274
|
|
|
histiocytic dermatoarthritis
|
[NCBI]
|
0.000193274
|
|
|
cardiac lipidosis, familial
|
[NCBI]
|
0.000193274
|
|
|
histiocytosis, progressive mucinous
|
[NCBI]
|
0.000193274
|
|
|
gm1-gangliosidosis, type i
|
[NCBI]
|
0.000190299
|
|
|
ceroid storage disease
|
[NCBI]
|
0.000154028
|
|
|
hyaluronidase deficiency
|
[NCBI]
|
0.000154028
|
|
|
hyaluronan metabolism, defect in
|
[NCBI]
|
0.000154028
|
|
|
gaucher disease, type i
|
[NCBI]
|
0.000148386
|
|
|
CGD
|
[NCBI]
|
0.000131012
|
|
|
thrombocytopenic purpura, autoimmune
|
[NCBI]
|
0.000125576
|
|
|
TGD
|
[NCBI]
|
8.13673e-05
|
|
|
HFTC
|
[NCBI]
|
8.13673e-05
|
|
|
mucopolysaccharidosis type vi
|
[NCBI]
|
7.86617e-05
|
|
|
granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type i
|
[NCBI]
|
7.28899e-05
|
|
|
sandhoff disease
|
[NCBI]
|
6.48808e-05
|
|
|
CLN3
|
[NCBI]
|
6.41243e-05
|
|
|
RA
|
[NCBI]
|
6.13814e-05
|
|
|
neuraminidase deficiency
|
[NCBI]
|
5.53544e-05
|
|
|
mucolipidosis ii
|
[NCBI]
|
5.28327e-05
|
|
|
HYAL1
|
[NCBI]
|
4.81194e-05
|
|
|
DBA
|
[NCBI]
|
4.57832e-05
|
|
|
GALNT3
|
[NCBI]
|
4.36465e-05
|
|
|
BMP5
|
[NCBI]
|
4.36465e-05
|
|
|
AACT
|
[NCBI]
|
4.01921e-05
|
|
|
ZS
|
[NCBI]
|
3.73893e-05
|
|
|
FUS
|
[NCBI]
|
3.61187e-05
|
|
|
DFSP
|
[NCBI]
|
3.59305e-05
|
|
|
CYBB
|
[NCBI]
|
3.32718e-05
|
|
|
fucosidosis
|
[NCBI]
|
3.2768e-05
|
|
|
TNFRSF6
|
[NCBI]
|
3.22974e-05
|
|
|
MTCYB
|
[NCBI]
|
3.20733e-05
|
|
|
wolman disease
|
[NCBI]
|
3.01506e-05
|
|
|
neuraminidase deficiency with beta-galactosidase deficiency
|
[NCBI]
|
3.01506e-05
|
|
|
TYR
|
[NCBI]
|
2.77432e-05
|
|
|
TNF
|
[NCBI]
|
2.69607e-05
|
|
|
CCL22
|
[NCBI]
|
2.4911e-05
|
|
|
CHS
|
[NCBI]
|
2.41603e-05
|
|
|
temporal arteritis
|
[NCBI]
|
1.90098e-05
|
|
|
AT
|
[NCBI]
|
1.76808e-05
|
|
|
PCNA
|
[NCBI]
|
1.34579e-05
|
|
|
ALD
|
[NCBI]
|
1.18252e-05
|
|
|
ACP5
|
[NCBI]
|
1.16676e-05
|
|
|
SPP1
|
[NCBI]
|
9.24655e-06
|
|
|
ADA
|
[NCBI]
|
8.4073e-06
|
|
|
TNFSF6
|
[NCBI]
|
6.62932e-06
|
|
|
KLK3
|
[NCBI]
|
5.74078e-06
|
|
|
HGF
|
[NCBI]
|
3.6556e-06
|
|
|
SLE
|
[NCBI]
|
3.69775e-08
|
|
|
VEGF
|
[NCBI]
|
1.70262e-08
|
|