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: C0031557
Disease: Phlegmon
Phlegmon 		1 0 1 0.17 0 0
CUI: C0155526
Disease: Cochlear otosclerosis
Cochlear otosclerosis 		1 0 1 0.17 0 0
CUI: C0266004
Disease: Knuckle pads, leuconychia and sensorineural deafness
Knuckle pads, leuconychia and sensorineural deafness 		1 0 1 0.17 0 0
CUI: C0280301
Disease: Hard Palate Squamous Cell Carcinoma
Hard Palate Squamous Cell Carcinoma 		1 0 1 0.17 0 0
CUI: C0393602
Disease: Isolated cervical dystonia
Isolated cervical dystonia 		1 0 1 0.17 0 0
CUI: C0395976
Disease: Hearing loss associated with syndrome
Hearing loss associated with syndrome 		1 0 1 0.17 0 0
CUI: C0473577
Disease: Eccrine nevus
Eccrine nevus 		1 0 1 0.17 0 0
CUI: C0473579
Disease: Porokeratotic eccrine ostial and dermal duct nevus
Porokeratotic eccrine ostial and dermal duct nevus 		1 0 1 0.17 0 0
CUI: C0473582
Disease: Hair follicle nevus
Hair follicle nevus 		1 0 1 0.17 0 0
CUI: C0478084
Disease: Other congenital ichthyosis
Other congenital ichthyosis 		1 0 1 0.17 0 0
CUI: C0544795
Disease: Follicular occlusion triad - hidradenitis, acne conglobata, dissecting cellulitis of scalp
Follicular occlusion triad - hidradenitis, acne conglobata, dissecting cellulitis of scalp 		1 0 1 0.17 0 0
CUI: C0730364
Disease: Idiopathic polypoidal choroidal vasculopathy
Idiopathic polypoidal choroidal vasculopathy 		1 0 1 0.17 0 0
CUI: C1275100
Disease: Keratoderma with deafness
Keratoderma with deafness 		1 0 1 0.17 0 0
CUI: C1843542
Disease: T-CELL PROLYMPHOCYTIC LEUKEMIA, SOMATIC
T-CELL PROLYMPHOCYTIC LEUKEMIA, SOMATIC 		1 0 1 0.17 0 0
CUI: C1859624
Disease: Defective B cell differentiation
Defective B cell differentiation 		1 0 1 0.17 0 0
CUI: C1865234
Disease: ICHTHYOSIS, HYSTRIX-LIKE, WITH DEAFNESS
ICHTHYOSIS, HYSTRIX-LIKE, WITH DEAFNESS 		1 0 1 0.17 0 0
CUI: C2315694
Disease: Bilateral sensory hearing loss
Bilateral sensory hearing loss 		1 0 1 0.17 0 0
CUI: C2675750
Disease: DEAFNESS, AUTOSOMAL DOMINANT 3A (disorder)
DEAFNESS, AUTOSOMAL DOMINANT 3A (disorder) 		1 0 1 0.17 0 0
CUI: C3825373
Disease: Hodgkin's disease in children
Hodgkin's disease in children 		1 0 1 0.17 0 0
CUI: C4023328
Disease: Abnormality of corneal stroma
Abnormality of corneal stroma 		1 0 1 0.17 0 0
CUI: C4748032
Disease: NEURODEVELOPMENTAL DISORDER WITH CEREBELLAR ATROPHY AND WITH OR WITHOUT SEIZURES
NEURODEVELOPMENTAL DISORDER WITH CEREBELLAR ATROPHY AND WITH OR WITHOUT SEIZURES 		1 4 1 0.17 2 0.12
CUI: C1876175
Disease: Ataxia-Telangiectasia Variant
Ataxia-Telangiectasia Variant 		2 0 1 0.14 0 0
CUI: C2675235
Disease: Deafness, Autosomal Recessive 1b
Deafness, Autosomal Recessive 1b 		2 0 1 0.14 0 0
CUI: C4017102
Disease: ATAXIA-TELANGIECTASIA WITHOUT IMMUNODEFICIENCY
ATAXIA-TELANGIECTASIA WITHOUT IMMUNODEFICIENCY 		2 0 1 0.14 0 0
CUI: C4021065
Disease: Fullness of paranasal tissue
Fullness of paranasal tissue 		2 0 1 0.14 0 0