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: C2675236
Disease: Deafness, Autosomal Dominant 2B
Deafness, Autosomal Dominant 2B 		2 0 2 0.67 0 0
CUI: C2673759
Disease: DEAFNESS, AUTOSOMAL RECESSIVE 1A (disorder)
DEAFNESS, AUTOSOMAL RECESSIVE 1A (disorder) 		4 0 2 0.40 0 0
CUI: C2673761
Disease: DEAFNESS, DIGENIC, GJB2/GJB3 (disorder)
DEAFNESS, DIGENIC, GJB2/GJB3 (disorder) 		4 0 2 0.40 0 0
CUI: C0010334
Disease: Crisscross Heart
Crisscross Heart 		1 0 1 0.33 0 0
CUI: C0232259
Disease: Mid-systolic murmur
Mid-systolic murmur 		1 0 1 0.33 0 0
CUI: C0349477
Disease: Transient neonatal hypothyroidism
Transient neonatal hypothyroidism 		1 0 1 0.33 0 0
CUI: C0409939
Disease: Osteoarthritis of glenohumeral joint
Osteoarthritis of glenohumeral joint 		1 0 1 0.33 0 0
CUI: C0553668
Disease: Labored breathing
Labored breathing 		1 0 1 0.33 0 0
CUI: C1834056
Disease: Thin anteverted nares
Thin anteverted nares 		1 0 1 0.33 0 0
CUI: C1834057
Disease: Vertebral hyperostosis
Vertebral hyperostosis 		1 0 1 0.33 0 0
CUI: C1851480
Disease: Greither Disease
Greither Disease 		1 0 1 0.33 0 0
CUI: C1857508
Disease: Patchy sclerosis of finger phalanx
Patchy sclerosis of finger phalanx 		1 0 1 0.33 0 0
CUI: C1861366
Disease: SYNDACTYLY, TYPE III
SYNDACTYLY, TYPE III 		1 0 1 0.33 0 0
CUI: C1863093
Disease: Alopecia congenita keratosis palmoplantaris
Alopecia congenita keratosis palmoplantaris 		1 0 1 0.33 0 0
CUI: C2749477
Disease: Oculodentodigital Dysplasia, Autosomal Recessive
Oculodentodigital Dysplasia, Autosomal Recessive 		1 0 1 0.33 0 0
CUI: C2931577
Disease: Basaran Yilmaz syndrome
Basaran Yilmaz syndrome 		1 0 1 0.33 0 0
CUI: C3148751
Disease: DEAFNESS, AUTOSOMAL DOMINANT, WITH PERIPHERAL NEUROPATHY
DEAFNESS, AUTOSOMAL DOMINANT, WITH PERIPHERAL NEUROPATHY 		1 0 1 0.33 0 0
CUI: C3151468
Disease: PALMOPLANTAR KERATODERMA AND CONGENITAL ALOPECIA 1
PALMOPLANTAR KERATODERMA AND CONGENITAL ALOPECIA 1 		1 0 1 0.33 0 0
CUI: C3275750
Disease: ATRIOVENTRICULAR SEPTAL DEFECT 3
ATRIOVENTRICULAR SEPTAL DEFECT 3 		1 0 1 0.33 0 0
CUI: C3277750
Disease: Absent middle phalanx of 5th finger
Absent middle phalanx of 5th finger 		1 0 1 0.33 0 0
CUI: C4021622
Disease: 2-4 toe cutaneous syndactyly
2-4 toe cutaneous syndactyly 		1 0 1 0.33 0 0
CUI: C4021633
Disease: Patchy palmoplantar keratoderma
Patchy palmoplantar keratoderma 		5 0 2 0.33 0 0
CUI: C4479619
Disease: ERYTHROKERATODERMIA VARIABILIS ET PROGRESSIVA 3
ERYTHROKERATODERMIA VARIABILIS ET PROGRESSIVA 3 		1 0 1 0.33 0 0
CUI: C4509933
Disease: Peripheral neuropathy with sensorineural hearing impairment syndrome
Peripheral neuropathy with sensorineural hearing impairment syndrome 		1 0 1 0.33 0 0
CUI: C1744601
Disease: Abnormal heart beat
Abnormal heart beat 		2 0 1 0.25 0 0