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: C0024900
Disease: Mastocytosis, Bullous
Mastocytosis, Bullous 		1 0 1 0.11 0 0
CUI: C0031557
Disease: Phlegmon
Phlegmon 		1 0 1 0.11 0 0
CUI: C0155526
Disease: Cochlear otosclerosis
Cochlear otosclerosis 		1 0 1 0.11 0 0
CUI: C0266004
Disease: Knuckle pads, leuconychia and sensorineural deafness
Knuckle pads, leuconychia and sensorineural deafness 		1 0 1 0.11 0 0
CUI: C0280301
Disease: Hard Palate Squamous Cell Carcinoma
Hard Palate Squamous Cell Carcinoma 		1 0 1 0.11 0 0
CUI: C0391816
Disease: Tietz syndrome
Tietz syndrome 		1 0 1 0.11 0 0
CUI: C0395976
Disease: Hearing loss associated with syndrome
Hearing loss associated with syndrome 		1 0 1 0.11 0 0
CUI: C0473577
Disease: Eccrine nevus
Eccrine nevus 		1 0 1 0.11 0 0
CUI: C0473579
Disease: Porokeratotic eccrine ostial and dermal duct nevus
Porokeratotic eccrine ostial and dermal duct nevus 		1 0 1 0.11 0 0
CUI: C0473582
Disease: Hair follicle nevus
Hair follicle nevus 		1 0 1 0.11 0 0
CUI: C0478084
Disease: Other congenital ichthyosis
Other congenital ichthyosis 		1 0 1 0.11 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 0.11 0 0
CUI: C1275100
Disease: Keratoderma with deafness
Keratoderma with deafness 		1 0 1 0.11 0 0
CUI: C1335911
Disease: Salivary Gland Sialoblastoma
Salivary Gland Sialoblastoma 		1 0 1 0.11 0 0
CUI: C1835039
Disease: Melanosis, Universal
Melanosis, Universal 		1 0 1 0.11 0 0
CUI: C1837203
Disease: WAARDENBURG SYNDROME, TYPE IID
WAARDENBURG SYNDROME, TYPE IID 		1 0 1 0.11 0 0
CUI: C1838099
Disease: ABCD syndrome
ABCD syndrome 		1 0 1 0.11 0 0
CUI: C1838564
Disease: HIRSCHSPRUNG DISEASE, SUSCEPTIBILITY TO, 2
HIRSCHSPRUNG DISEASE, SUSCEPTIBILITY TO, 2 		1 0 1 0.11 0 0
CUI: C1852510
Disease: Craniofacial deafness hand syndrome
Craniofacial deafness hand syndrome 		1 0 1 0.11 0 0
CUI: C1861799
Disease: Catatrichy
Catatrichy 		1 0 1 0.11 0 0
CUI: C1865234
Disease: ICHTHYOSIS, HYSTRIX-LIKE, WITH DEAFNESS
ICHTHYOSIS, HYSTRIX-LIKE, WITH DEAFNESS 		1 0 1 0.11 0 0
CUI: C1866425
Disease: Yemenite deaf-blind hypopigmentation syndrome
Yemenite deaf-blind hypopigmentation syndrome 		1 0 1 0.11 0 0
CUI: C2315694
Disease: Bilateral sensory hearing loss
Bilateral sensory hearing loss 		1 0 1 0.11 0 0
CUI: C2675750
Disease: DEAFNESS, AUTOSOMAL DOMINANT 3A (disorder)
DEAFNESS, AUTOSOMAL DOMINANT 3A (disorder) 		1 0 1 0.11 0 0
CUI: C2750457
Disease: Waardenburg Syndrome, Type 4b
Waardenburg Syndrome, Type 4b 		1 0 1 0.11 0 0