Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
Muscular Dystrophy, Facioscapulohumeral
143 0 14 7.9E-02 0 0
CUI: C0677936
Disease: Refractory cancer
Refractory cancer
184 0 17 7.9E-02 0 0
Refractory anemia with ringed sideroblasts
36 0 6 7.7E-02 0 0
CUI: C0410438
Disease: Primary osteoporosis
Primary osteoporosis
23 0 5 7.6E-02 0 0
CUI: C0949541
Disease: Hurthle Cell Tumor
Hurthle Cell Tumor
170 0 15 7.4E-02 0 0
CUI: C0234378
Disease: Static Tremor
Static Tremor
62 0 7 6.8E-02 0 0
CUI: C4721411
Disease: Osteolysis
Osteolysis
62 0 7 6.8E-02 0 0
CUI: C0272170
Disease: Shwachman syndrome
Shwachman syndrome
49 0 6 6.6E-02 0 0
CUI: C0730328
Disease: Central Serous Chorioretinopathy
Central Serous Chorioretinopathy
211 0 16 6.6E-02 0 0
CUI: C0020651
Disease: Hypotension, Orthostatic
Hypotension, Orthostatic
82 0 8 6.6E-02 0 0
Disruptive, Impulse Control, and Conduct Disorders
67 0 7 6.5E-02 0 0
CUI: C0574002
Disease: Edema of foot (finding)
Edema of foot (finding)
19 0 4 6.3E-02 0 0
CUI: C0270736
Disease: Essential Tremor
Essential Tremor
122 79 10 6.2E-02 1 5.0E-03
CUI: C0809983
Disease: Schizophrenia and related disorders
Schizophrenia and related disorders
20 0 4 6.2E-02 0 0
Myelodysplastic-Myeloproliferative Diseases
38 0 5 6.2E-02 0 0
CUI: C0858321
Disease: Plasmodium vivax infection
Plasmodium vivax infection
21 0 4 6.2E-02 0 0
CUI: C3160718
Disease: PARKINSON DISEASE, LATE-ONSET
PARKINSON DISEASE, LATE-ONSET
247 76 17 6.1E-02 11 5.8E-02
CUI: C0035372
Disease: Rett Syndrome
Rett Syndrome
234 0 16 6.0E-02 0 0
CUI: C0037061
Disease: Siderosis
Siderosis
23 0 4 6.0E-02 0 0
CUI: C2931245
Disease: Bone Marrow failure syndromes
Bone Marrow failure syndromes
41 0 5 6.0E-02 0 0
CUI: C0153633
Disease: Malignant neoplasm of brain
Malignant neoplasm of brain
294 0 19 5.9E-02 0 0
CUI: C0748052
Disease: Erythrodermic psoriasis
Erythrodermic psoriasis
6 0 3 5.9E-02 0 0
Therapy-related myelodysplastic syndrome
42 0 5 5.9E-02 0 0
CUI: C0038868
Disease: Progressive supranuclear palsy
Progressive supranuclear palsy
176 0 12 5.7E-02 0 0
CUI: C0878682
Disease: Ceruloplasmin deficiency
Ceruloplasmin deficiency
8 0 3 5.7E-02 0 0