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: C1838263
Disease: Deafness, Autosomal Recessive 3
Deafness, Autosomal Recessive 3
1 69 1 6.1E-03 6 4.7E-02
DEAFNESS, AUTOSOMAL DOMINANT 3A (disorder)
1 49 1 6.1E-03 5 4.5E-02
Palmoplantar Keratoderma with Deafness
3 27 3 1.8E-02 4 4.5E-02
CUI: C0339789
Disease: Congenital deafness
Congenital deafness
72 11 31 0.15 3 4.1E-02
CUI: C2675235
Disease: Deafness, Autosomal Recessive 1b
Deafness, Autosomal Recessive 1b
2 16 2 1.2E-02 3 3.8E-02
ICHTHYOSIS, HYSTRIX-LIKE, WITH DEAFNESS
1 20 1 6.1E-03 3 3.6E-02
Knuckle pads, leuconychia and sensorineural deafness
1 21 1 6.1E-03 3 3.6E-02
Nodular Sclerosis Classical Hodgkin Lymphoma
66 22 19 9.0E-02 3 3.5E-02
CUI: C0265964
Disease: Mutilating keratoderma
Mutilating keratoderma
9 24 1 5.8E-03 3 3.4E-02
CUI: C1384666
Disease: hearing impairment
hearing impairment
740 337 110 0.14 13 3.3E-02
CUI: C0265336
Disease: Senter syndrome
Senter syndrome
4 30 2 1.2E-02 3 3.2E-02
DEAFNESS, AUTOSOMAL RECESSIVE 1A (disorder)
4 98 4 2.5E-02 5 3.1E-02
Progressive hearing loss stapes fixation
4 35 4 2.5E-02 3 3.1E-02
Sensorineural Hearing Loss (disorder)
783 111 102 0.12 5 2.9E-02
CUI: C1568249
Disease: Usher Syndrome, Type II
Usher Syndrome, Type II
12 7 7 4.2E-02 2 2.8E-02
JERVELL AND LANGE-NIELSEN SYNDROME 2 (disorder)
1 7 1 6.1E-03 2 2.8E-02
CUI: C3887873
Disease: Hearing Loss
Hearing Loss
18 61 7 4.0E-02 3 2.4E-02
CUI: C0023264
Disease: Leigh Disease
Leigh Disease
144 114 5 1.7E-02 3 1.7E-02
CUI: C1824925
Disease: DEAFNESS, AUTOSOMAL RECESSIVE 70
DEAFNESS, AUTOSOMAL RECESSIVE 70
1 1 1 6.1E-03 1 1.5E-02
CUI: C2829267
Disease: DEAFNESS, AUTOSOMAL RECESSIVE 88
DEAFNESS, AUTOSOMAL RECESSIVE 88
1 1 1 6.1E-03 1 1.5E-02
CUI: C2931210
Disease: Usher syndrome, type 1F
Usher syndrome, type 1F
2 1 2 1.2E-02 1 1.5E-02
CUI: C3279948
Disease: DEAFNESS, AUTOSOMAL DOMINANT 64
DEAFNESS, AUTOSOMAL DOMINANT 64
1 1 1 6.1E-03 1 1.5E-02
CUI: C0011052
Disease: Prelingual Deafness
Prelingual Deafness
22 2 14 8.2E-02 1 1.5E-02
CUI: C1148477
Disease: Deafness, Sudden
Deafness, Sudden
6 2 1 6.0E-03 1 1.5E-02
DEAFNESS, AUTOSOMAL DOMINANT 41 (disorder)
1 2 1 6.1E-03 1 1.5E-02