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: C4707897
Disease: Severe early-onset axonal neuropathy due to mitofusin 2 deficiency
Severe early-onset axonal neuropathy due to mitofusin 2 deficiency 		1 0 1 7.7E-02 0 0
CUI: C4721887
Disease: CHARCOT-MARIE-TOOTH DISEASE, AXONAL, AUTOSOMAL DOMINANT, TYPE 2A2A
CHARCOT-MARIE-TOOTH DISEASE, AXONAL, AUTOSOMAL DOMINANT, TYPE 2A2A 		1 0 1 7.7E-02 0 0
CUI: C0023801
Disease: Lipomatosis
Lipomatosis 		16 0 2 7.4E-02 0 0
CUI: C0038828
Disease: Superior Mesenteric Artery Syndrome
Superior Mesenteric Artery Syndrome 		2 0 1 7.1E-02 0 0
CUI: C0155096
Disease: Corneal ghost vessels
Corneal ghost vessels 		2 0 1 7.1E-02 0 0
CUI: C0268354
Disease: De Barsy syndrome
De Barsy syndrome 		2 0 1 7.1E-02 0 0
CUI: C0311262
Disease: Chronic mesenteric ischemia
Chronic mesenteric ischemia 		2 0 1 7.1E-02 0 0
CUI: C0392477
Disease: Congenital flat foot
Congenital flat foot 		2 0 1 7.1E-02 0 0
CUI: C0549159
Disease: Infant Death
Infant Death 		2 0 1 7.1E-02 0 0
CUI: C0751865
Disease: Alcohol-Induced Disorders, Nervous System
Alcohol-Induced Disorders, Nervous System 		2 0 1 7.1E-02 0 0
CUI: C0751914
Disease: Adult Pelizaeus-Merzbacher Disease
Adult Pelizaeus-Merzbacher Disease 		2 0 1 7.1E-02 0 0
CUI: C0751915
Disease: Pelizaeus-Merzbacher Disease, Atypical
Pelizaeus-Merzbacher Disease, Atypical 		2 0 1 7.1E-02 0 0
CUI: C0751916
Disease: Classic Pelizaeus-Merzbacher Disease
Classic Pelizaeus-Merzbacher Disease 		2 0 1 7.1E-02 0 0
CUI: C0751917
Disease: Pelizaeus-Merzbacher Disease, Transitional
Pelizaeus-Merzbacher Disease, Transitional 		2 0 1 7.1E-02 0 0
CUI: C0751918
Disease: Cockayne-Pelizaeus-Merzbacher Disease
Cockayne-Pelizaeus-Merzbacher Disease 		2 0 1 7.1E-02 0 0
CUI: C1112321
Disease: Congenital cutis laxa
Congenital cutis laxa 		2 0 1 7.1E-02 0 0
CUI: C1263886
Disease: Neoplasm of frontal lobe
Neoplasm of frontal lobe 		2 0 1 7.1E-02 0 0
CUI: C1370500
Disease: Tanycytic ependymoma
Tanycytic ependymoma 		2 0 1 7.1E-02 0 0
CUI: C1403880
Disease: Viral meningoencephalitis
Viral meningoencephalitis 		2 0 1 7.1E-02 0 0
CUI: C1838230
Disease: SPINAL MUSCULAR ATROPHY, TYPE IV
SPINAL MUSCULAR ATROPHY, TYPE IV 		2 0 1 7.1E-02 0 0
CUI: C1863704
Disease: Spastic paraplegia 8, autosomal dominant
Spastic paraplegia 8, autosomal dominant 		2 0 1 7.1E-02 0 0
CUI: C1868524
Disease: Autonomic erectile dysfunction
Autonomic erectile dysfunction 		2 0 1 7.1E-02 0 0
CUI: C2721580
Disease: Breakthrough cancer pain
Breakthrough cancer pain 		2 0 1 7.1E-02 0 0
CUI: C2751987
Disease: Cutis Laxa, Autosomal Recessive, Type IIB
Cutis Laxa, Autosomal Recessive, Type IIB 		2 0 1 7.1E-02 0 0
CUI: C3151147
Disease: Bile Acid Synthesis Defect, Congenital, 3
Bile Acid Synthesis Defect, Congenital, 3 		2 0 1 7.1E-02 0 0