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: C0558353
Disease: Tongue Carcinoma
Tongue Carcinoma 		0 2 0 0 1 3.2E-02
CUI: C0812437
Disease: Oculo-dento-digital syndrome
Oculo-dento-digital syndrome 		0 22 0 0 1 2.0E-02
CUI: C1834055
Disease: Underdeveloped nasal alae
Underdeveloped nasal alae 		0 8 0 0 1 2.7E-02
CUI: C0031557
Disease: Phlegmon
Phlegmon 		1 0 1 0.25 0 0
CUI: C0155526
Disease: Cochlear otosclerosis
Cochlear otosclerosis 		1 0 1 0.25 0 0
CUI: C0266004
Disease: Knuckle pads, leuconychia and sensorineural deafness
Knuckle pads, leuconychia and sensorineural deafness 		1 21 1 0.25 20 0.65
CUI: C0280301
Disease: Hard Palate Squamous Cell Carcinoma
Hard Palate Squamous Cell Carcinoma 		1 0 1 0.25 0 0
CUI: C0395976
Disease: Hearing loss associated with syndrome
Hearing loss associated with syndrome 		1 0 1 0.25 0 0
CUI: C0473577
Disease: Eccrine nevus
Eccrine nevus 		1 0 1 0.25 0 0
CUI: C0473579
Disease: Porokeratotic eccrine ostial and dermal duct nevus
Porokeratotic eccrine ostial and dermal duct nevus 		1 2 1 0.25 2 6.7E-02
CUI: C0473582
Disease: Hair follicle nevus
Hair follicle nevus 		1 0 1 0.25 0 0
CUI: C0478084
Disease: Other congenital ichthyosis
Other congenital ichthyosis 		1 0 1 0.25 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 0.25 0 0
CUI: C1266060
Disease: Syringofibroadenoma
Syringofibroadenoma 		1 0 1 0.25 0 0
CUI: C1275100
Disease: Keratoderma with deafness
Keratoderma with deafness 		1 0 1 0.25 0 0
CUI: C1863734
Disease: Caudal interpedicular narrowing
Caudal interpedicular narrowing 		1 0 1 0.25 0 0
CUI: C1865234
Disease: ICHTHYOSIS, HYSTRIX-LIKE, WITH DEAFNESS
ICHTHYOSIS, HYSTRIX-LIKE, WITH DEAFNESS 		1 20 1 0.25 20 0.67
CUI: C2315694
Disease: Bilateral sensory hearing loss
Bilateral sensory hearing loss 		1 0 1 0.25 0 0
CUI: C2675237
Disease: Deafness, Autosomal Dominant 3B
Deafness, Autosomal Dominant 3B 		1 4 1 0.25 1 3.0E-02
CUI: C2675750
Disease: DEAFNESS, AUTOSOMAL DOMINANT 3A (disorder)
DEAFNESS, AUTOSOMAL DOMINANT 3A (disorder) 		1 49 1 0.25 20 0.34
CUI: C4021597
Disease: Delayed patellar ossification
Delayed patellar ossification 		1 0 1 0.25 0 0
CUI: C4021609
Disease: Delayed phalangeal epiphyseal ossification
Delayed phalangeal epiphyseal ossification 		1 0 1 0.25 0 0
CUI: C4021865
Disease: Long distal phalanx of finger
Long distal phalanx of finger 		1 0 1 0.25 0 0
CUI: C4022961
Disease: Slender proximal phalanx of finger
Slender proximal phalanx of finger 		1 0 1 0.25 0 0
CUI: C4022962
Disease: Slender distal phalanx of finger
Slender distal phalanx of finger 		1 0 1 0.25 0 0