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: C2673759
Disease: DEAFNESS, AUTOSOMAL RECESSIVE 1A (disorder)
DEAFNESS, AUTOSOMAL RECESSIVE 1A (disorder) 		4 98 4 5.4E-03 41 0.10
CUI: C3538946
Disease: DEAFNESS, AUTOSOMAL RECESSIVE 4, WITH ENLARGED VESTIBULAR AQUEDUCT
DEAFNESS, AUTOSOMAL RECESSIVE 4, WITH ENLARGED VESTIBULAR AQUEDUCT 		10 81 7 9.4E-03 38 1.0E-01
CUI: C3887873
Disease: Hearing Loss
Hearing Loss 		18 61 11 1.5E-02 26 7.0E-02
CUI: C2675750
Disease: DEAFNESS, AUTOSOMAL DOMINANT 3A (disorder)
DEAFNESS, AUTOSOMAL DOMINANT 3A (disorder) 		1 49 1 1.4E-03 25 6.9E-02
CUI: C0271829
Disease: Pendred's syndrome
Pendred's syndrome 		35 142 16 2.1E-02 24 5.3E-02
CUI: C0018784
Disease: Sensorineural Hearing Loss (disorder)
Sensorineural Hearing Loss (disorder) 		783 111 270 0.22 21 4.9E-02
CUI: C1835672
Disease: Palmoplantar Keratoderma with Deafness
Palmoplantar Keratoderma with Deafness 		3 27 3 4.1E-03 17 4.9E-02
CUI: C1865234
Disease: ICHTHYOSIS, HYSTRIX-LIKE, WITH DEAFNESS
ICHTHYOSIS, HYSTRIX-LIKE, WITH DEAFNESS 		1 20 1 1.4E-03 16 4.7E-02
CUI: C0265336
Disease: Senter syndrome
Senter syndrome 		4 30 2 2.7E-03 16 4.6E-02
CUI: C0266004
Disease: Knuckle pads, leuconychia and sensorineural deafness
Knuckle pads, leuconychia and sensorineural deafness 		1 21 1 1.4E-03 15 4.4E-02
CUI: C0265964
Disease: Mutilating keratoderma
Mutilating keratoderma 		9 24 2 2.7E-03 15 4.3E-02
CUI: C1844678
Disease: Progressive hearing loss stapes fixation
Progressive hearing loss stapes fixation 		4 35 4 5.4E-03 15 4.2E-02
CUI: C1832394
Disease: Deafness, Autosomal Recessive 12
Deafness, Autosomal Recessive 12 		4 57 4 5.4E-03 15 4.0E-02
CUI: C1838263
Disease: Deafness, Autosomal Recessive 3
Deafness, Autosomal Recessive 3 		1 69 1 1.4E-03 15 3.8E-02
CUI: C1832828
Disease: Deafness, Autosomal Recessive 9
Deafness, Autosomal Recessive 9 		5 88 4 5.4E-03 15 3.7E-02
CUI: C2675235
Disease: Deafness, Autosomal Recessive 1b
Deafness, Autosomal Recessive 1b 		2 16 2 2.7E-03 12 3.5E-02
CUI: C3711374
Disease: Nonsyndromic Deafness
Nonsyndromic Deafness 		163 66 110 0.14 13 3.3E-02
CUI: C4551563
Disease: Microcephaly (physical finding)
Microcephaly (physical finding) 		160 246 36 4.2E-02 10 1.7E-02
CUI: C1853276
Disease: Deafness, Autosomal Recessive 28
Deafness, Autosomal Recessive 28 		2 15 1 1.3E-03 6 1.7E-02
CUI: C1838701
Disease: DEAFNESS, AUTOSOMAL RECESSIVE 2
DEAFNESS, AUTOSOMAL RECESSIVE 2 		7 135 7 9.5E-03 8 1.7E-02
CUI: C2931213
Disease: Usher syndrome, type 2C
Usher syndrome, type 2C 		4 28 2 2.7E-03 6 1.7E-02
CUI: C0454644
Disease: Delayed speech and language development
Delayed speech and language development 		560 192 103 8.6E-02 8 1.5E-02
CUI: C0423318
Disease: Heterochromia iridis
Heterochromia iridis 		17 10 12 1.6E-02 5 1.5E-02
CUI: C1836830
Disease: Developmental regression
Developmental regression 		333 80 76 7.6E-02 6 1.5E-02
CUI: C0423110
Disease: Downward slant of palpebral fissure
Downward slant of palpebral fissure 		391 49 127 0.13 5 1.3E-02