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: C0008521
Disease: Choroid Diseases
Choroid Diseases 		1 0 1 0.17 0 0
CUI: C0026244
Disease: Mitochondrial Swelling
Mitochondrial Swelling 		1 0 1 0.17 0 0
CUI: C0345218
Disease: Low anorectal malformation
Low anorectal malformation 		1 0 1 0.17 0 0
CUI: C1333502
Disease: extragonadal seminoma
extragonadal seminoma 		1 0 1 0.17 0 0
CUI: C3280556
Disease: PERIPHERAL NEUROPATHY, MYOPATHY, HOARSENESS, AND HEARING LOSS
PERIPHERAL NEUROPATHY, MYOPATHY, HOARSENESS, AND HEARING LOSS 		1 0 1 0.17 0 0
CUI: C3554592
Disease: MICROPHTHALMIA, ISOLATED, WITH COLOBOMA 9
MICROPHTHALMIA, ISOLATED, WITH COLOBOMA 9 		1 0 1 0.17 0 0
CUI: C4225296
Disease: MENTAL RETARDATION, AUTOSOMAL DOMINANT 39
MENTAL RETARDATION, AUTOSOMAL DOMINANT 39 		1 0 1 0.17 0 0
CUI: C0262963
Disease: extragonadal germ cell tumor
extragonadal germ cell tumor 		2 0 1 0.14 0 0
CUI: C1833503
Disease: Deafness, Autosomal Dominant 4
Deafness, Autosomal Dominant 4 		2 0 1 0.14 0 0
CUI: C4024765
Disease: Peripapillary chorioretinal atrophy
Peripapillary chorioretinal atrophy 		2 0 1 0.14 0 0
CUI: C2936864
Disease: Bardet-Biedl syndrome 4 (disorder)
Bardet-Biedl syndrome 4 (disorder) 		4 0 1 0.11 0 0
CUI: C4023965
Disease: Structural foot deformity
Structural foot deformity 		5 0 1 1.0E-01 0 0
CUI: C0848765
Disease: Hearing disability
Hearing disability 		6 0 1 9.1E-02 0 0
CUI: C0175713
Disease: Aicardi's syndrome
Aicardi's syndrome 		7 0 1 8.3E-02 0 0
CUI: C0854078
Disease: Diabetic end stage renal disease
Diabetic end stage renal disease 		7 0 1 8.3E-02 0 0
CUI: C1842160
Disease: MYOPATHY, MYOSIN STORAGE (disorder)
MYOPATHY, MYOSIN STORAGE (disorder) 		7 0 1 8.3E-02 0 0
CUI: C2931501
Disease: Microphthalmia associated with colobomatous cyst
Microphthalmia associated with colobomatous cyst 		8 0 1 7.7E-02 0 0
CUI: C2931500
Disease: Microphthalmia and mental deficiency
Microphthalmia and mental deficiency 		9 0 1 7.1E-02 0 0
CUI: C4255043
Disease: Microphthalmos co-occurrent with congenital ocular coloboma
Microphthalmos co-occurrent with congenital ocular coloboma 		9 0 1 7.1E-02 0 0
CUI: C0027401
Disease: Narcissism
Narcissism 		10 0 1 6.7E-02 0 0
CUI: C4505353
Disease: Diverticular Bleeding
Diverticular Bleeding 		13 0 1 5.6E-02 0 0
CUI: C1836609
Disease: Progressive distal muscle weakness
Progressive distal muscle weakness 		14 0 1 5.3E-02 0 0
CUI: C4021082
Disease: Fatty replacement of skeletal muscle
Fatty replacement of skeletal muscle 		17 0 1 4.5E-02 0 0
CUI: C0016508
Disease: Congenital Foot Deformity
Congenital Foot Deformity 		18 0 1 4.3E-02 0 0
CUI: C0265594
Disease: Congenital absence of hand
Congenital absence of hand 		18 0 1 4.3E-02 0 0