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: C0345958
Disease: Large cell carcinoma of lung
Large cell carcinoma of lung 		67 0 6 7.3E-02 0 0
CUI: C0263662
Disease: Disseminated eosinophilic collagen disease
Disseminated eosinophilic collagen disease 		14 0 2 6.1E-02 0 0
CUI: C3150773
Disease: CHROMOSOME 8p11 MYELOPROLIFERATIVE SYNDROME
CHROMOSOME 8p11 MYELOPROLIFERATIVE SYNDROME 		17 0 2 5.6E-02 0 0
CUI: C1540912
Disease: Hypereosinophilic syndrome
Hypereosinophilic syndrome 		19 0 2 5.3E-02 0 0
CUI: C0749379
Disease: Thoracolumbar scoliosis
Thoracolumbar scoliosis 		20 0 2 5.1E-02 0 0
CUI: C1332213
Disease: Adult T Lymphoblastic Lymphoma
Adult T Lymphoblastic Lymphoma 		21 0 2 5.0E-02 0 0
CUI: C1332998
Disease: Childhood T Lymphoblastic Lymphoma
Childhood T Lymphoblastic Lymphoma 		21 0 2 5.0E-02 0 0
CUI: C0262477
Disease: Eye problem
Eye problem 		1 0 1 4.8E-02 0 0
CUI: C0278714
Disease: stage IV Wilms tumor
stage IV Wilms tumor 		1 0 1 4.8E-02 0 0
CUI: C0432149
Disease: Lumbar hemivertebra
Lumbar hemivertebra 		1 0 1 4.8E-02 0 0
CUI: C0558384
Disease: Arthritis/arthrosis
Arthritis/arthrosis 		1 0 1 4.8E-02 0 0
CUI: C0796046
Disease: Gurrieri Sammito Bellussi syndrome
Gurrieri Sammito Bellussi syndrome 		1 0 1 4.8E-02 0 0
CUI: C1333286
Disease: Diencephalic Neoplasm
Diencephalic Neoplasm 		1 0 1 4.8E-02 0 0
CUI: C1845146
Disease: Holoprosencephaly, Ectrodactyly, and Bilateral Cleft Lip-Palate
Holoprosencephaly, Ectrodactyly, and Bilateral Cleft Lip-Palate 		1 0 1 4.8E-02 0 0
CUI: C1856231
Disease: Thin calvarium
Thin calvarium 		1 0 1 4.8E-02 0 0
CUI: C1856911
Disease: Ivory epiphyses
Ivory epiphyses 		1 0 1 4.8E-02 0 0
CUI: C1859478
Disease: Hypoplasia of proximal fibula
Hypoplasia of proximal fibula 		1 0 1 4.8E-02 0 0
CUI: C1866182
Disease: Penttinen-Aula syndrome
Penttinen-Aula syndrome 		1 0 1 4.8E-02 0 0
CUI: C3281203
Disease: CUTANEOUS TELANGIECTASIA AND CANCER SYNDROME, FAMILIAL
CUTANEOUS TELANGIECTASIA AND CANCER SYNDROME, FAMILIAL 		1 0 1 4.8E-02 0 0
CUI: C3472621
Disease: Myeloid neoplasm with beta-type platelet-derived growth factor receptor gene rearrangement
Myeloid neoplasm with beta-type platelet-derived growth factor receptor gene rearrangement 		1 0 1 4.8E-02 0 0
CUI: C3554321
Disease: BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 4
BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 4 		1 0 1 4.8E-02 0 0
CUI: C3711560
Disease: Pdgfrb-Associated Chronic Eosinophilic Leukemia
Pdgfrb-Associated Chronic Eosinophilic Leukemia 		1 0 1 4.8E-02 0 0
CUI: C3843745
Disease: Squamous cell (epidermoid) carcinoma
Squamous cell (epidermoid) carcinoma 		1 0 1 4.8E-02 0 0
CUI: C4016104
Disease: HYPOGONADOTROPIC HYPOGONADISM 2 WITH ANOSMIA
HYPOGONADOTROPIC HYPOGONADISM 2 WITH ANOSMIA 		1 0 1 4.8E-02 0 0
CUI: C4016940
Disease: AMYOTROPHIC LATERAL SCLEROSIS-PARKINSONISM/DEMENTIA COMPLEX 1, SUSCEPTIBILITY TO
AMYOTROPHIC LATERAL SCLEROSIS-PARKINSONISM/DEMENTIA COMPLEX 1, SUSCEPTIBILITY TO 		1 0 1 4.8E-02 0 0