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: C0009761
Disease: Conjunctival Neoplasms
Conjunctival Neoplasms 		1 0 1 1.3E-02 0 0
CUI: C0019250
Disease: Hereditary factor I deficiency disease
Hereditary factor I deficiency disease 		1 0 1 1.3E-02 0 0
CUI: C0023138
Disease: Laurence-Moon Syndrome
Laurence-Moon Syndrome 		1 0 1 1.3E-02 0 0
CUI: C0031557
Disease: Phlegmon
Phlegmon 		1 0 1 1.3E-02 0 0
CUI: C0035290
Disease: Reticulohistiocytic granuloma
Reticulohistiocytic granuloma 		1 0 1 1.3E-02 0 0
CUI: C0037050
Disease: Sick Building Syndrome
Sick Building Syndrome 		1 0 1 1.3E-02 0 0
CUI: C0155526
Disease: Cochlear otosclerosis
Cochlear otosclerosis 		1 0 1 1.3E-02 0 0
CUI: C0155563
Disease: Rheumatic mitral regurgitation
Rheumatic mitral regurgitation 		1 0 1 1.3E-02 0 0
CUI: C0162504
Disease: Neutrophilic Eccrine Hidradenitis
Neutrophilic Eccrine Hidradenitis 		1 0 1 1.3E-02 0 0
CUI: C0231691
Disease: Cerebellar Gait Ataxia
Cerebellar Gait Ataxia 		1 0 1 1.3E-02 0 0
CUI: C0235328
Disease: Obstruction of colon
Obstruction of colon 		1 0 1 1.3E-02 0 0
CUI: C0236656
Disease: Dementia associated with alcoholism
Dementia associated with alcoholism 		1 0 1 1.3E-02 0 0
CUI: C0263583
Disease: Idiopathic guttate hypomelanosis
Idiopathic guttate hypomelanosis 		1 0 1 1.3E-02 0 0
CUI: C0266004
Disease: Knuckle pads, leuconychia and sensorineural deafness
Knuckle pads, leuconychia and sensorineural deafness 		1 0 1 1.3E-02 0 0
CUI: C0266564
Disease: Congenital anomaly of retina
Congenital anomaly of retina 		1 0 1 1.3E-02 0 0
CUI: C0266571
Disease: Congenital retinal aneurysm
Congenital retinal aneurysm 		1 0 1 1.3E-02 0 0
CUI: C0268371
Disease: Epidermolysis Bullosa With Congenital Localized Absence Of Skin And Deformity Of Nails
Epidermolysis Bullosa With Congenital Localized Absence Of Skin And Deformity Of Nails 		1 0 1 1.3E-02 0 0
CUI: C0271285
Disease: Epithelial basement membrane dystrophy
Epithelial basement membrane dystrophy 		1 0 1 1.3E-02 0 0
CUI: C0272241
Disease: Complement abnormality
Complement abnormality 		1 0 1 1.3E-02 0 0
CUI: C0272263
Disease: Cryofibrinogenemia
Cryofibrinogenemia 		1 0 1 1.3E-02 0 0
CUI: C0278600
Disease: Childhood Brain Stem Glioma
Childhood Brain Stem Glioma 		1 0 1 1.3E-02 0 0
CUI: C0280301
Disease: Hard Palate Squamous Cell Carcinoma
Hard Palate Squamous Cell Carcinoma 		1 0 1 1.3E-02 0 0
CUI: C0302323
Disease: Reticulohistiocytosis
Reticulohistiocytosis 		1 0 1 1.3E-02 0 0
CUI: C0332778
Disease: Diastasis, Bone
Diastasis, Bone 		1 0 1 1.3E-02 0 0
CUI: C0339271
Disease: Salzmann nodular dystrophy
Salzmann nodular dystrophy 		1 0 1 1.3E-02 0 0