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: C4021065
Disease: Fullness of paranasal tissue
Fullness of paranasal tissue 		2 2 2 0.67 2 1.00
CUI: C1845878
Disease: Irregularly spaced teeth
Irregularly spaced teeth 		3 2 2 0.50 2 1.00
CUI: C4025316
Disease: Temporal hypotrichosis
Temporal hypotrichosis 		3 2 2 0.50 2 1.00
CUI: C0031557
Disease: Phlegmon
Phlegmon 		1 0 1 0.33 0 0
CUI: C0155526
Disease: Cochlear otosclerosis
Cochlear otosclerosis 		1 0 1 0.33 0 0
CUI: C0266004
Disease: Knuckle pads, leuconychia and sensorineural deafness
Knuckle pads, leuconychia and sensorineural deafness 		1 21 1 0.33 1 4.5E-02
CUI: C0280301
Disease: Hard Palate Squamous Cell Carcinoma
Hard Palate Squamous Cell Carcinoma 		1 0 1 0.33 0 0
CUI: C0395976
Disease: Hearing loss associated with syndrome
Hearing loss associated with syndrome 		1 0 1 0.33 0 0
CUI: C0473577
Disease: Eccrine nevus
Eccrine nevus 		1 0 1 0.33 0 0
CUI: C0473579
Disease: Porokeratotic eccrine ostial and dermal duct nevus
Porokeratotic eccrine ostial and dermal duct nevus 		1 0 1 0.33 0 0
CUI: C0473582
Disease: Hair follicle nevus
Hair follicle nevus 		1 0 1 0.33 0 0
CUI: C0478084
Disease: Other congenital ichthyosis
Other congenital ichthyosis 		1 0 1 0.33 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 0.33 0 0
CUI: C1275100
Disease: Keratoderma with deafness
Keratoderma with deafness 		1 0 1 0.33 0 0
CUI: C1865234
Disease: ICHTHYOSIS, HYSTRIX-LIKE, WITH DEAFNESS
ICHTHYOSIS, HYSTRIX-LIKE, WITH DEAFNESS 		1 20 1 0.33 1 4.8E-02
CUI: C2315694
Disease: Bilateral sensory hearing loss
Bilateral sensory hearing loss 		1 0 1 0.33 0 0
CUI: C2675750
Disease: DEAFNESS, AUTOSOMAL DOMINANT 3A (disorder)
DEAFNESS, AUTOSOMAL DOMINANT 3A (disorder) 		1 49 1 0.33 1 2.0E-02
CUI: C3553247
Disease: MENTAL RETARDATION, AUTOSOMAL DOMINANT 14
MENTAL RETARDATION, AUTOSOMAL DOMINANT 14 		1 0 1 0.33 0 0
CUI: C4014528
Disease: MENTAL RETARDATION, AUTOSOMAL DOMINANT 27
MENTAL RETARDATION, AUTOSOMAL DOMINANT 27 		1 5 1 0.33 1 0.17
CUI: C4023328
Disease: Abnormality of corneal stroma
Abnormality of corneal stroma 		1 0 1 0.33 0 0
CUI: C1836674
Disease: Short distal phalanx of the 5th finger
Short distal phalanx of the 5th finger 		6 2 2 0.29 2 1.00
CUI: C0265837
Disease: Congenital hypoplasia of tricuspid valve
Congenital hypoplasia of tricuspid valve 		2 0 1 0.25 0 0
CUI: C1302454
Disease: Complex atypical endometrial hyperplasia
Complex atypical endometrial hyperplasia 		2 0 1 0.25 0 0
CUI: C2675235
Disease: Deafness, Autosomal Recessive 1b
Deafness, Autosomal Recessive 1b 		2 16 1 0.25 1 5.9E-02
CUI: C4020917
Disease: Absent fifth fingernail
Absent fifth fingernail 		2 0 1 0.25 0 0