|
OMIM |
Link |
Information
gain |
01 |
|
|
hemophagocytic lymphohistiocytosis, familial, 1
|
[NCBI]
|
0.0159475
|
|
|
|
letterer-siwe disease
|
[NCBI]
|
0.00117822
|
|
|
|
histiocytosis, familial lipochrome
|
[NCBI]
|
0.000938218
|
|
|
|
reticuloendotheliosis, x-linked
|
[NCBI]
|
0.000938218
|
|
|
|
omenn syndrome
|
[NCBI]
|
0.000524429
|
|
|
|
sea-blue histiocyte disease
|
[NCBI]
|
0.000313496
|
|
|
|
histiocytosis, progressive mucinous
|
[NCBI]
|
0.000115876
|
|
|
|
histiocytic dermatoarthritis
|
[NCBI]
|
0.000115876
|
|
|
|
kindler syndrome
|
[NCBI]
|
8.25826e-05
|
|
|
|
CSF1R
|
[NCBI]
|
7.34161e-05
|
|
|
|
cerebrotendinous xanthomatosis
|
[NCBI]
|
6.68256e-05
|
|
|
|
TGD
|
[NCBI]
|
6.48401e-05
|
|
|
|
CGD
|
[NCBI]
|
5.08554e-05
|
|
|
|
hla-d histocompatibility type
|
[NCBI]
|
4.2561e-05
|
|
|
|
thrombocytopenic purpura, autoimmune
|
[NCBI]
|
4.10122e-05
|
|
|
|
WAS
|
[NCBI]
|
3.03253e-05
|
|
|
|
MUC1
|
[NCBI]
|
3.01679e-05
|
|
|
|
GFAP
|
[NCBI]
|
1.98624e-05
|
|
|
|
RA
|
[NCBI]
|
1.46004e-05
|
|
