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: C1334282
Disease: Inverted urothelial papilloma
Inverted urothelial papilloma 		0 3 0 0 1 5.3E-03
CUI: C3887608
Disease: HYDROCEPHALUS, NONSYNDROMIC, AUTOSOMAL RECESSIVE 1
HYDROCEPHALUS, NONSYNDROMIC, AUTOSOMAL RECESSIVE 1 		0 6 0 0 2 1.0E-02
CUI: C0009761
Disease: Conjunctival Neoplasms
Conjunctival Neoplasms 		1 0 1 1.2E-02 0 0
CUI: C0016697
Disease: Freemartinism
Freemartinism 		1 0 1 1.2E-02 0 0
CUI: C0023441
Disease: Leukemia, Experimental
Leukemia, Experimental 		1 0 1 1.2E-02 0 0
CUI: C0030215
Disease: Palatal Neoplasms
Palatal Neoplasms 		1 0 1 1.2E-02 0 0
CUI: C0034184
Disease: Pyelocystitis
Pyelocystitis 		1 0 1 1.2E-02 0 0
CUI: C0035290
Disease: Reticulohistiocytic granuloma
Reticulohistiocytic granuloma 		1 0 1 1.2E-02 0 0
CUI: C0151482
Disease: Megaloblastic anemia due to folate deficiency
Megaloblastic anemia due to folate deficiency 		1 0 1 1.2E-02 0 0
CUI: C0152190
Disease: Refractive amblyopia
Refractive amblyopia 		1 1 1 1.2E-02 1 5.3E-03
CUI: C0152499
Disease: Acute amebiasis
Acute amebiasis 		1 0 1 1.2E-02 0 0
CUI: C0153470
Disease: Malignant neoplasm of spleen
Malignant neoplasm of spleen 		1 0 1 1.2E-02 0 0
CUI: C0154064
Disease: Carcinoma in situ of anus
Carcinoma in situ of anus 		1 0 1 1.2E-02 0 0
CUI: C0162164
Disease: Congenital stenosis of pulmonary valve
Congenital stenosis of pulmonary valve 		1 3 1 1.2E-02 3 1.6E-02
CUI: C0162504
Disease: Neutrophilic Eccrine Hidradenitis
Neutrophilic Eccrine Hidradenitis 		1 0 1 1.2E-02 0 0
CUI: C0202220
Disease: Somatomedin-C measurement
Somatomedin-C measurement 		1 0 1 1.2E-02 0 0
CUI: C0232308
Disease: P pulmonale by EKG (finding)
P pulmonale by EKG (finding) 		1 0 1 1.2E-02 0 0
CUI: C0235410
Disease: Potassium retention
Potassium retention 		1 0 1 1.2E-02 0 0
CUI: C0239894
Disease: HEART DISPLACEMENT
HEART DISPLACEMENT 		1 0 1 1.2E-02 0 0
CUI: C0242012
Disease: NEPHROTIC SYNDROME, CHRONIC
NEPHROTIC SYNDROME, CHRONIC 		1 0 1 1.2E-02 0 0
CUI: C0262477
Disease: Eye problem
Eye problem 		1 0 1 1.2E-02 0 0
CUI: C0265248
Disease: Ruvalcaba Syndrome
Ruvalcaba Syndrome 		1 0 1 1.2E-02 0 0
CUI: C0265833
Disease: Congenital insufficiency of pulmonary valve
Congenital insufficiency of pulmonary valve 		1 1 1 1.2E-02 1 5.3E-03
CUI: C0271618
Disease: Delayed female puberty
Delayed female puberty 		1 0 1 1.2E-02 0 0
CUI: C0271629
Disease: Mullerian inhibiting factor deficiency
Mullerian inhibiting factor deficiency 		1 0 1 1.2E-02 0 0