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: C4551486
Disease: ERYTHROKERATODERMIA VARIABILIS ET PROGRESSIVA 1
ERYTHROKERATODERMIA VARIABILIS ET PROGRESSIVA 1 		3 0 2 0.67 0 0
CUI: C1851480
Disease: Greither Disease
Greither Disease 		1 0 1 0.50 0 0
CUI: C2673759
Disease: DEAFNESS, AUTOSOMAL RECESSIVE 1A (disorder)
DEAFNESS, AUTOSOMAL RECESSIVE 1A (disorder) 		4 0 2 0.50 0 0
CUI: C2673761
Disease: DEAFNESS, DIGENIC, GJB2/GJB3 (disorder)
DEAFNESS, DIGENIC, GJB2/GJB3 (disorder) 		4 0 2 0.50 0 0
CUI: C3148751
Disease: DEAFNESS, AUTOSOMAL DOMINANT, WITH PERIPHERAL NEUROPATHY
DEAFNESS, AUTOSOMAL DOMINANT, WITH PERIPHERAL NEUROPATHY 		1 0 1 0.50 0 0
CUI: C4509933
Disease: Peripheral neuropathy with sensorineural hearing impairment syndrome
Peripheral neuropathy with sensorineural hearing impairment syndrome 		1 0 1 0.50 0 0
CUI: C4479618
Disease: ERYTHROKERATODERMIA VARIABILIS ET PROGRESSIVA 2
ERYTHROKERATODERMIA VARIABILIS ET PROGRESSIVA 2 		2 0 1 0.33 0 0
CUI: C2673760
Disease: DEAFNESS, DIGENIC, GJB2/GJB6 (disorder)
DEAFNESS, DIGENIC, GJB2/GJB6 (disorder) 		3 0 1 0.25 0 0
CUI: C2750327
Disease: Hearing loss, sensorineural (high frequency)
Hearing loss, sensorineural (high frequency) 		3 0 1 0.25 0 0
CUI: C4021633
Disease: Patchy palmoplantar keratoderma
Patchy palmoplantar keratoderma 		5 0 1 0.17 0 0
CUI: C0265961
Disease: Erythrokeratodermia variabilis
Erythrokeratodermia variabilis 		13 8 2 0.15 1 0.11
CUI: C0395971
Disease: Dominant sensorineural hearing loss
Dominant sensorineural hearing loss 		6 0 1 0.14 0 0
CUI: C4022756
Disease: Profound hearing impairment
Profound hearing impairment 		7 0 1 0.12 0 0
CUI: C0392553
Disease: Hereditary peripheral neuropathy
Hereditary peripheral neuropathy 		9 0 1 1.0E-01 0 0
CUI: C1852581
Disease: EPILEPSY, BENIGN NEONATAL, 2
EPILEPSY, BENIGN NEONATAL, 2 		9 0 1 1.0E-01 0 0
CUI: C3889476
Disease: Benign Familial Convulsion
Benign Familial Convulsion 		9 0 1 1.0E-01 0 0
CUI: C0432330
Disease: Erythrokeratoderma
Erythrokeratoderma 		10 0 1 9.1E-02 0 0
CUI: C0859886
Disease: Inherited hearing loss
Inherited hearing loss 		13 0 1 7.1E-02 0 0
CUI: C1691779
Disease: Sensory hearing loss
Sensory hearing loss 		14 0 1 6.7E-02 0 0
CUI: C1969913
Disease: Generalized hyperkeratosis
Generalized hyperkeratosis 		16 0 1 5.9E-02 0 0
CUI: C3279547
Disease: Hypergranulosis
Hypergranulosis 		16 0 1 5.9E-02 0 0
CUI: C1846647
Disease: DEAFNESS, AUTOSOMAL RECESSIVE (disorder)
DEAFNESS, AUTOSOMAL RECESSIVE (disorder) 		38 4 2 5.3E-02 1 0.20
CUI: C0079153
Disease: Hyperkeratosis, Epidermolytic
Hyperkeratosis, Epidermolytic 		20 0 1 4.8E-02 0 0
CUI: C0086395
Disease: Hearing Loss, Extreme
Hearing Loss, Extreme 		20 0 1 4.8E-02 0 0
CUI: C0581883
Disease: Complete Hearing Loss
Complete Hearing Loss 		20 0 1 4.8E-02 0 0