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: C0742115
Disease: Cerebritis
Cerebritis 		1 0 1 6.2E-02 0 0
CUI: C0742608
Disease: colon (non-specific) polyp hyperplastic
colon (non-specific) polyp hyperplastic 		1 0 1 6.2E-02 0 0
CUI: C0751071
Disease: Familial Dementia
Familial Dementia 		18 0 2 6.2E-02 0 0
CUI: C0856322
Disease: Alcoholic brain damage
Alcoholic brain damage 		1 0 1 6.2E-02 0 0
CUI: C1328061
Disease: Myelodysplastic/myeloproliferative neoplasm, unclassifiable
Myelodysplastic/myeloproliferative neoplasm, unclassifiable 		1 0 1 6.2E-02 0 0
CUI: C1516553
Disease: Prefibrotic/Early Primary Myelofibrosis
Prefibrotic/Early Primary Myelofibrosis 		1 0 1 6.2E-02 0 0
CUI: C1833021
Disease: DEAFNESS, AUTOSOMAL DOMINANT 6
DEAFNESS, AUTOSOMAL DOMINANT 6 		1 0 1 6.2E-02 0 0
CUI: C1837429
Disease: Pyruvate dehydrogenase phosphatase deficiency
Pyruvate dehydrogenase phosphatase deficiency 		1 0 1 6.2E-02 0 0
CUI: C1839888
Disease: Decreased activity of the pyruvate dehydrogenase complex
Decreased activity of the pyruvate dehydrogenase complex 		35 0 3 6.2E-02 0 0
CUI: C1840646
Disease: Hepatic Adenomas, Familial
Hepatic Adenomas, Familial 		1 0 1 6.2E-02 0 0
CUI: C1843014
Disease: Alzheimer Disease, Familial, 3, with Spastic Paraparesis and Unusual Plaques
Alzheimer Disease, Familial, 3, with Spastic Paraparesis and Unusual Plaques 		1 0 1 6.2E-02 0 0
CUI: C1843015
Disease: Alzheimer Disease, Familial, 3, with Spastic Paraparesis and Apraxia
Alzheimer Disease, Familial, 3, with Spastic Paraparesis and Apraxia 		1 0 1 6.2E-02 0 0
CUI: C1857288
Disease: Limited mobility of proximal interphalangeal joint
Limited mobility of proximal interphalangeal joint 		1 0 1 6.2E-02 0 0
CUI: C1960396
Disease: Epidermal growth factor receptor negative non-small cell lung cancer
Epidermal growth factor receptor negative non-small cell lung cancer 		1 0 1 6.2E-02 0 0
CUI: C2675105
Disease: BUDD-CHIARI SYNDROME, SUSCEPTIBILITY TO, SOMATIC
BUDD-CHIARI SYNDROME, SUSCEPTIBILITY TO, SOMATIC 		1 0 1 6.2E-02 0 0
CUI: C2751494
Disease: CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED, ARCTIC VARIANT
CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED, ARCTIC VARIANT 		1 0 1 6.2E-02 0 0
CUI: C2751536
Disease: CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED
CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED 		1 0 1 6.2E-02 0 0
CUI: C3151038
Disease: ACNE INVERSA, FAMILIAL, 3
ACNE INVERSA, FAMILIAL, 3 		1 0 1 6.2E-02 0 0
CUI: C3160720
Disease: Cardiomyopathy, Dilated, 1u
Cardiomyopathy, Dilated, 1u 		1 0 1 6.2E-02 0 0
CUI: C3280358
Disease: Wolfram-Like Syndrome, Autosomal Dominant
Wolfram-Like Syndrome, Autosomal Dominant 		1 0 1 6.2E-02 0 0
CUI: C3281125
Disease: THROMBOCYTHEMIA 3
THROMBOCYTHEMIA 3 		1 0 1 6.2E-02 0 0
CUI: C3282903
Disease: Metastatic Carcinoma in the Liver
Metastatic Carcinoma in the Liver 		1 0 1 6.2E-02 0 0
CUI: C3544080
Disease: Congenital central diabetes insipidus
Congenital central diabetes insipidus 		1 0 1 6.2E-02 0 0
CUI: C3805412
Disease: CATARACT 41
CATARACT 41 		1 0 1 6.2E-02 0 0
CUI: C3810445
Disease: Low-frequency sensorineural hearing impairment
Low-frequency sensorineural hearing impairment 		1 0 1 6.2E-02 0 0