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: C1266186
Disease: Retinoblastoma, spontaneously regressed
Retinoblastoma, spontaneously regressed 		12 0 12 1.00 0 0
CUI: C0341747
Disease: Detrusor and sphincter dyssynergia
Detrusor and sphincter dyssynergia 		12 0 8 0.50 0 0
CUI: C1568363
Disease: Tendinosis
Tendinosis 		28 0 8 0.25 0 0
CUI: C0017150
Disease: Gastrinoma
Gastrinoma 		49 0 8 0.15 0 0
CUI: C0206718
Disease: Ganglioneuroblastoma
Ganglioneuroblastoma 		57 0 9 0.15 0 0
CUI: C0282513
Disease: Primary Progressive Aphasia (disorder)
Primary Progressive Aphasia (disorder) 		51 0 8 0.15 0 0
CUI: C0036349
Disease: Paranoid Schizophrenia
Paranoid Schizophrenia 		53 0 8 0.14 0 0
CUI: C0549493
Disease: Alveolitis
Alveolitis 		63 0 8 0.12 0 0
CUI: C1334953
Disease: Neuroblastic tumors
Neuroblastic tumors 		73 0 9 0.12 0 0
CUI: C0280220
Disease: stage, ovarian epithelial cancer
stage, ovarian epithelial cancer 		65 0 8 0.12 0 0
CUI: C0017075
Disease: Ganglioneuroma
Ganglioneuroma 		88 0 9 9.9E-02 0 0
CUI: C1522378
Disease: Leukemia, Large Granular Lymphocytic
Leukemia, Large Granular Lymphocytic 		78 0 8 9.8E-02 0 0
CUI: C0751483
Disease: Familial Retinoblastoma
Familial Retinoblastoma 		12 0 2 9.1E-02 0 0
CUI: C1275126
Disease: TNF receptor-associated periodic fever syndrome (TRAPS)
TNF receptor-associated periodic fever syndrome (TRAPS) 		90 0 8 8.5E-02 0 0
CUI: C0020474
Disease: Hyperlipidemia, Familial Combined
Hyperlipidemia, Familial Combined 		91 0 8 8.4E-02 0 0
CUI: C0264878
Disease: Heart valve stenosis
Heart valve stenosis 		1 0 1 8.3E-02 0 0
CUI: C0809936
Disease: Branchio-skeleto-genital syndrome
Branchio-skeleto-genital syndrome 		1 0 1 8.3E-02 0 0
CUI: C1517445
Disease: Ganglioneuroblastoma, Nodular
Ganglioneuroblastoma, Nodular 		1 0 1 8.3E-02 0 0
CUI: C1863870
Disease: Hypospadias, Hypertelorism, Upper Lid Coloboma, and Mixed-Type Hearing Loss
Hypospadias, Hypertelorism, Upper Lid Coloboma, and Mixed-Type Hearing Loss 		1 0 1 8.3E-02 0 0
CUI: C4021299
Disease: Abnormality of dentin
Abnormality of dentin 		1 0 1 8.3E-02 0 0
CUI: C4021828
Disease: Advanced pneumatization of the mastoid process
Advanced pneumatization of the mastoid process 		1 0 1 8.3E-02 0 0
CUI: C4024197
Disease: Amelia involving the lower limbs
Amelia involving the lower limbs 		1 0 1 8.3E-02 0 0
CUI: C4024199
Disease: Upper limb peromelia
Upper limb peromelia 		1 0 1 8.3E-02 0 0
CUI: C4073208
Disease: Abnormality of the shape of the midface
Abnormality of the shape of the midface 		1 0 1 8.3E-02 0 0
CUI: C4310786
Disease: AGAMMAGLOBULINEMIA 8, AUTOSOMAL DOMINANT
AGAMMAGLOBULINEMIA 8, AUTOSOMAL DOMINANT 		1 0 1 8.3E-02 0 0