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 5.0E-02 0 0
CUI: C0151463
Disease: Abscess of breast
Abscess of breast
1 0 1 5.0E-02 0 0
CUI: C0155526
Disease: Cochlear otosclerosis
Cochlear otosclerosis
1 0 1 5.0E-02 0 0
CUI: C0235863
Disease: Delayed delivery
Delayed delivery
1 0 1 5.0E-02 0 0
Knuckle pads, leuconychia and sensorineural deafness
1 0 1 5.0E-02 0 0
CUI: C0280301
Disease: Hard Palate Squamous Cell Carcinoma
Hard Palate Squamous Cell Carcinoma
1 0 1 5.0E-02 0 0
CUI: C0391816
Disease: Tietz syndrome
Tietz syndrome
1 0 1 5.0E-02 0 0
Hearing loss associated with syndrome
1 0 1 5.0E-02 0 0
CUI: C0456086
Disease: Intrapartum fetal hypoxia
Intrapartum fetal hypoxia
1 0 1 5.0E-02 0 0
CUI: C0473577
Disease: Eccrine nevus
Eccrine nevus
1 0 1 5.0E-02 0 0
Porokeratotic eccrine ostial and dermal duct nevus
1 0 1 5.0E-02 0 0
CUI: C0473582
Disease: Hair follicle nevus
Hair follicle nevus
1 0 1 5.0E-02 0 0
CUI: C0478084
Disease: Other congenital ichthyosis
Other congenital ichthyosis
1 0 1 5.0E-02 0 0
Follicular occlusion triad - hidradenitis, acne conglobata, dissecting cellulitis of scalp
1 0 1 5.0E-02 0 0
CUI: C0571550
Disease: Allergy to vaccine
Allergy to vaccine
1 0 1 5.0E-02 0 0
CUI: C0751696
Disease: Post-Traumatic Vegetative State
Post-Traumatic Vegetative State
1 0 1 5.0E-02 0 0
CUI: C0858353
Disease: Addicted to heroin
Addicted to heroin
1 0 1 5.0E-02 0 0
CUI: C0865304
Disease: Schizophreniform psychosis NOS
Schizophreniform psychosis NOS
1 0 1 5.0E-02 0 0
CUI: C0865573
Disease: Mitral disease
Mitral disease
1 0 1 5.0E-02 0 0
CUI: C1275100
Disease: Keratoderma with deafness
Keratoderma with deafness
1 0 1 5.0E-02 0 0
CUI: C1282908
Disease: De Vaal's syndrome
De Vaal's syndrome
1 0 1 5.0E-02 0 0
CUI: C1389273
Disease: Lesions in the basal ganglia
Lesions in the basal ganglia
1 0 1 5.0E-02 0 0
Auditory Neuropathy, Nonsyndromic Recessive
1 0 1 5.0E-02 0 0
JUVENILE POLYPOSIS/HEREDITARY HEMORRHAGIC TELANGIECTASIA SYNDROME (disorder)
1 0 1 5.0E-02 0 0
CUI: C1836027
Disease: Deafness, Autosomal Recessive 23
Deafness, Autosomal Recessive 23
1 0 1 5.0E-02 0 0