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: C0079037
Disease: Branchial Clefts-Congenital disorder
Branchial Clefts-Congenital disorder 		1 0 1 7.1E-02 0 0
CUI: C0158651
Disease: Cleft lip, unilateral, complete
Cleft lip, unilateral, complete 		1 0 1 7.1E-02 0 0
CUI: C0241633
Disease: Vaginal dryness
Vaginal dryness 		1 0 1 7.1E-02 0 0
CUI: C0395905
Disease: Postauricular fistula
Postauricular fistula 		1 0 1 7.1E-02 0 0
CUI: C0406716
Disease: Hypodontia and nail dysgenesis
Hypodontia and nail dysgenesis 		1 0 1 7.1E-02 0 0
CUI: C0543612
Disease: Cervical syndrome
Cervical syndrome 		1 0 1 7.1E-02 0 0
CUI: C0810363
Disease: Cleft palate without cleft lip
Cleft palate without cleft lip 		1 0 1 7.1E-02 0 0
CUI: C1302999
Disease: Ankyloblepharon filiforme adnatum
Ankyloblepharon filiforme adnatum 		1 0 1 7.1E-02 0 0
CUI: C1332865
Disease: Cavernous Sinus Meningioma
Cavernous Sinus Meningioma 		1 0 1 7.1E-02 0 0
CUI: C1449718
Disease: Endocrine Breast Diseases
Endocrine Breast Diseases 		1 0 1 7.1E-02 0 0
CUI: C1833538
Disease: OROFACIAL CLEFT 7
OROFACIAL CLEFT 7 		1 0 1 7.1E-02 0 0
CUI: C1837213
Disease: OROFACIAL CLEFT 6, SUSCEPTIBILITY TO
OROFACIAL CLEFT 6, SUSCEPTIBILITY TO 		1 0 1 7.1E-02 0 0
CUI: C1851878
Disease: OROFACIAL CLEFT 8
OROFACIAL CLEFT 8 		1 0 1 7.1E-02 0 0
CUI: C1851885
Disease: Progressive alopecia
Progressive alopecia 		1 0 1 7.1E-02 0 0
CUI: C1854594
Disease: DEAFNESS, AUTOSOMAL DOMINANT 23
DEAFNESS, AUTOSOMAL DOMINANT 23 		1 0 1 7.1E-02 0 0
CUI: C1857048
Disease: Progressive hypotrichosis
Progressive hypotrichosis 		1 0 1 7.1E-02 0 0
CUI: C1858562
Disease: ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME 3
ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME 3 		1 0 1 7.1E-02 0 0
CUI: C1862059
Disease: Supraauricular pit
Supraauricular pit 		1 0 1 7.1E-02 0 0
CUI: C1862066
Disease: Branchial anomaly
Branchial anomaly 		1 0 1 7.1E-02 0 0
CUI: C1862068
Disease: Fusion of middle ear ossicles
Fusion of middle ear ossicles 		1 0 1 7.1E-02 0 0
CUI: C1862858
Disease: Red, cracking, peeling skin at birth
Red, cracking, peeling skin at birth 		1 0 1 7.1E-02 0 0
CUI: C1865092
Disease: TOOTH AGENESIS, SELECTIVE, 2 (disorder)
TOOTH AGENESIS, SELECTIVE, 2 (disorder) 		1 0 1 7.1E-02 0 0
CUI: C1963268
Disease: Vaginal Dryness, CTCAE 3.0
Vaginal Dryness, CTCAE 3.0 		1 0 1 7.1E-02 0 0
CUI: C2749019
Disease: JOUBERT SYNDROME 10 (disorder)
JOUBERT SYNDROME 10 (disorder) 		1 0 1 7.1E-02 0 0
CUI: C3275495
Disease: KABUKI SYNDROME 2
KABUKI SYNDROME 2 		1 0 1 7.1E-02 0 0