Source: ALL
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: C0151311
Disease: Cranial nerve palsies
Cranial nerve palsies 		0 1 0 0 1 0.50
CUI: C0242073
Disease: Pulmonary congestion
Pulmonary congestion 		0 1 0 0 1 0.50
CUI: C0272275
Disease: Heparin-induced thrombocytopenia with thrombosis
Heparin-induced thrombocytopenia with thrombosis 		0 1 0 0 1 0.50
CUI: C0272285
Disease: Heparin-induced thrombocytopenia
Heparin-induced thrombocytopenia 		0 5 0 0 1 0.17
CUI: C0002890
Disease: Leukoerythroblastic Anemia
Leukoerythroblastic Anemia 		1 1 1 7.1E-02 1 0.50
CUI: C0041315
Disease: Tuberculosis, Laryngeal
Tuberculosis, Laryngeal 		1 0 1 7.1E-02 0 0
CUI: C0262477
Disease: Eye problem
Eye problem 		1 0 1 7.1E-02 0 0
CUI: C0276658
Disease: Infection by Aspergillus flavus
Infection by Aspergillus flavus 		1 0 1 7.1E-02 0 0
CUI: C0278714
Disease: stage IV Wilms tumor
stage IV Wilms tumor 		1 0 1 7.1E-02 0 0
CUI: C0334113
Disease: Eosinophilic granulomatous polyp
Eosinophilic granulomatous polyp 		1 0 1 7.1E-02 0 0
CUI: C0343101
Disease: Wells syndrome
Wells syndrome 		1 0 1 7.1E-02 0 0
CUI: C0432149
Disease: Lumbar hemivertebra
Lumbar hemivertebra 		1 0 1 7.1E-02 0 0
CUI: C0518964
Disease: BRONCHIAL ADENOCARCINOMA
BRONCHIAL ADENOCARCINOMA 		1 0 1 7.1E-02 0 0
CUI: C0948384
Disease: Cerebral hygroma
Cerebral hygroma 		1 0 1 7.1E-02 0 0
CUI: C1096446
Disease: Slight temperature
Slight temperature 		1 0 1 7.1E-02 0 0
CUI: C1328061
Disease: Myelodysplastic/myeloproliferative neoplasm, unclassifiable
Myelodysplastic/myeloproliferative neoplasm, unclassifiable 		1 1 1 7.1E-02 1 0.50
CUI: C1333286
Disease: Diencephalic Neoplasm
Diencephalic Neoplasm 		1 0 1 7.1E-02 0 0
CUI: C1335727
Disease: Refractory Mature T-Cell and NK-Cell Non-Hodgkin Lymphoma
Refractory Mature T-Cell and NK-Cell Non-Hodgkin Lymphoma 		1 0 1 7.1E-02 0 0
CUI: C1516553
Disease: Prefibrotic/Early Primary Myelofibrosis
Prefibrotic/Early Primary Myelofibrosis 		1 1 1 7.1E-02 1 0.50
CUI: C1838656
Disease: Macrocytosis, Familial
Macrocytosis, Familial 		1 0 1 7.1E-02 0 0
CUI: C1845146
Disease: Holoprosencephaly, Ectrodactyly, and Bilateral Cleft Lip-Palate
Holoprosencephaly, Ectrodactyly, and Bilateral Cleft Lip-Palate 		1 0 1 7.1E-02 0 0
CUI: C1855548
Disease: Laron syndrome type 2
Laron syndrome type 2 		1 0 1 7.1E-02 0 0
CUI: C1856231
Disease: Thin calvarium
Thin calvarium 		1 0 1 7.1E-02 0 0
CUI: C1866182
Disease: Penttinen-Aula syndrome
Penttinen-Aula syndrome 		1 0 1 7.1E-02 0 0
CUI: C1868000
Disease: Polyps, Multiple And Recurrent Inflammatory Fibroid, Gastrointestinal
Polyps, Multiple And Recurrent Inflammatory Fibroid, Gastrointestinal 		1 0 1 7.1E-02 0 0