Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
Keratosis Palmaris et Plantaris Familiaris
2 0 2 0.40 0 0
PALMOPLANTAR KERATODERMA, NONEPIDERMOLYTIC, FOCAL 1
2 0 2 0.40 0 0
CUI: C0031557
Disease: Phlegmon
Phlegmon
1 0 1 0.20 0 0
CUI: C0155526
Disease: Cochlear otosclerosis
Cochlear otosclerosis
1 0 1 0.20 0 0
Knuckle pads, leuconychia and sensorineural deafness
1 0 1 0.20 0 0
CUI: C0280301
Disease: Hard Palate Squamous Cell Carcinoma
Hard Palate Squamous Cell Carcinoma
1 0 1 0.20 0 0
Hearing loss associated with syndrome
1 0 1 0.20 0 0
CUI: C0473577
Disease: Eccrine nevus
Eccrine nevus
1 0 1 0.20 0 0
Porokeratotic eccrine ostial and dermal duct nevus
1 0 1 0.20 0 0
CUI: C0473582
Disease: Hair follicle nevus
Hair follicle nevus
1 0 1 0.20 0 0
CUI: C0478084
Disease: Other congenital ichthyosis
Other congenital ichthyosis
1 0 1 0.20 0 0
Follicular occlusion triad - hidradenitis, acne conglobata, dissecting cellulitis of scalp
1 0 1 0.20 0 0
CUI: C0549151
Disease: Follicular keratosis
Follicular keratosis
1 0 1 0.20 0 0
CUI: C1275100
Disease: Keratoderma with deafness
Keratoderma with deafness
1 0 1 0.20 0 0
Keratoderma, Palmoplantar, Epidermolytic
7 0 2 0.20 0 0
Hyperkeratosis, diffuse palmoplantar (tylosis)
1 0 1 0.20 0 0
Mottled pigmentation of the trunk and proximal extremities
1 0 1 0.20 0 0
Discrete 2 to 5-mm hyper- and hypopigmented macules
1 0 1 0.20 0 0
ICHTHYOSIS, HYSTRIX-LIKE, WITH DEAFNESS
1 0 1 0.20 0 0
CUI: C2315694
Disease: Bilateral sensory hearing loss
Bilateral sensory hearing loss
1 0 1 0.20 0 0
DEAFNESS, AUTOSOMAL DOMINANT 3A (disorder)
1 0 1 0.20 0 0
PALMOPLANTAR KERATODERMA, NONEPIDERMOLYTIC, FOCAL OR DIFFUSE
1 0 1 0.20 0 0
EPIDERMOLYSIS BULLOSA SIMPLEX, DOWLING-MEARA TYPE, WITH SEVERE PALMOPLANTAR KERATODERMA
1 0 1 0.20 0 0
EPIDERMOLYSIS BULLOSA SIMPLEX, GENERALIZED, WITH SEVERE PALMOPLANTAR KERATOSIS
1 0 1 0.20 0 0
CUI: C4023328
Disease: Abnormality of corneal stroma
Abnormality of corneal stroma
1 0 1 0.20 0 0