Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
CUI: C0206643
Disease: Neoplasms, Fibrous Tissue
Neoplasms, Fibrous Tissue
9 0 4 8.3E-02 0 0
Uterine tumor resembling ovarian sex cord tumor
6 0 3 6.5E-02 0 0
CUI: C1266134
Disease: Spindle cell rhabdomyosarcoma
Spindle cell rhabdomyosarcoma
9 0 3 6.1E-02 0 0
CUI: C0344460
Disease: Carcinoma ex pleomorphic adenoma
Carcinoma ex pleomorphic adenoma
30 0 4 5.8E-02 0 0
CUI: C0272170
Disease: Shwachman syndrome
Shwachman syndrome
49 0 5 5.7E-02 0 0
CUI: C1963099
Disease: Myelodysplasia, CTCAE
Myelodysplasia, CTCAE
68 0 6 5.7E-02 0 0
CUI: C0018922
Disease: hemangiopericytoma
hemangiopericytoma
32 0 4 5.6E-02 0 0
CUI: C4523989
Disease: Occult hepatitis B
Occult hepatitis B
14 0 3 5.6E-02 0 0
CUI: C1846546
Disease: Recurrent sinopulmonary infections
Recurrent sinopulmonary infections
16 0 3 5.4E-02 0 0
CUI: C0024899
Disease: Mastocytosis
Mastocytosis
98 0 7 5.2E-02 0 0
CUI: C0265965
Disease: Dyskeratosis Congenita
Dyskeratosis Congenita
58 0 5 5.2E-02 0 0
CUI: C4289709
Disease: DOCK8 Deficiency
DOCK8 Deficiency
18 0 3 5.2E-02 0 0
CUI: C0277527
Disease: Epidemic diarrhea
Epidemic diarrhea
19 0 3 5.1E-02 0 0
CUI: C1336052
Disease: Spindle Cell Neoplasm
Spindle Cell Neoplasm
19 0 3 5.1E-02 0 0
CUI: C1853118
Disease: Severe congenital neutropenia
Severe congenital neutropenia
66 0 5 4.8E-02 0 0
Generalized Thyroid Hormone Resistance
45 0 4 4.8E-02 0 0
CUI: C0340970
Disease: Congenital neutropenia
Congenital neutropenia
68 0 5 4.7E-02 0 0
CUI: C0349658
Disease: Trichoepithelioma
Trichoepithelioma
24 0 3 4.7E-02 0 0
Decreased number of small peripheral myelinated nerve fibers
2 0 2 4.7E-02 0 0
CUI: C0156344
Disease: Endometriosis of ovary
Endometriosis of ovary
70 0 5 4.6E-02 0 0
CUI: C1961835
Disease: Gaucher Disease, Type 1
Gaucher Disease, Type 1
48 0 4 4.6E-02 0 0
CUI: C1291129
Disease: Decreased reticulin
Decreased reticulin
3 0 2 4.5E-02 0 0
CUI: C1881236
Disease: Interstitial Disease
Interstitial Disease
3 0 2 4.5E-02 0 0
CUI: C0085620
Disease: Flaccid paralysis
Flaccid paralysis
4 0 2 4.4E-02 0 0
Neutropenia, Severe Congenital, X-Linked
4 0 2 4.4E-02 0 0