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: C0033735
Disease: Protothecosis
Protothecosis 		1 0 1 3.1E-02 0 0
CUI: C0039614
Disease: Tetanus
Tetanus 		1 0 1 3.1E-02 0 0
CUI: C0264955
Disease: Idiopathic arterial calcification of infancy
Idiopathic arterial calcification of infancy 		1 0 1 3.1E-02 0 0
CUI: C0268457
Disease: Aminoacidemia
Aminoacidemia 		1 0 1 3.1E-02 0 0
CUI: C0270217
Disease: Perinatal jaundice due to inspissated bile syndrome
Perinatal jaundice due to inspissated bile syndrome 		1 0 1 3.1E-02 0 0
CUI: C0270686
Disease: Fungal infection of brain
Fungal infection of brain 		1 0 1 3.1E-02 0 0
CUI: C0343881
Disease: Central nervous system candidiasis
Central nervous system candidiasis 		1 0 1 3.1E-02 0 0
CUI: C0343951
Disease: Disseminated phaeohyphomycosis
Disseminated phaeohyphomycosis 		1 0 1 3.1E-02 0 0
CUI: C0343957
Disease: Cutaneous mucormycosis
Cutaneous mucormycosis 		1 0 1 3.1E-02 0 0
CUI: C0349711
Disease: Sialic storage disease
Sialic storage disease 		1 0 1 3.1E-02 0 0
CUI: C0473117
Disease: Ischemic hepatitis
Ischemic hepatitis 		1 0 1 3.1E-02 0 0
CUI: C0554876
Disease: poorly controlled diabetes mellitus
poorly controlled diabetes mellitus 		1 0 1 3.1E-02 0 0
CUI: C0598121
Disease: Hypoglycorrhachia
Hypoglycorrhachia 		1 0 1 3.1E-02 0 0
CUI: C0683324
Disease: organic disease
organic disease 		1 0 1 3.1E-02 0 0
CUI: C0849963
Disease: Feeling nervous
Feeling nervous 		1 0 1 3.1E-02 0 0
CUI: C0854525
Disease: Post surgical diarrhea
Post surgical diarrhea 		1 0 1 3.1E-02 0 0
CUI: C0856217
Disease: Functional diarrhoea (due to spastic colon)
Functional diarrhoea (due to spastic colon) 		1 0 1 3.1E-02 0 0
CUI: C1167769
Disease: Candida endophthalmitis
Candida endophthalmitis 		1 0 1 3.1E-02 0 0
CUI: C1279621
Disease: Tinea profunda (disorder)
Tinea profunda (disorder) 		1 0 1 3.1E-02 0 0
CUI: C1395264
Disease: Deep seated dermatophytosis
Deep seated dermatophytosis 		1 0 1 3.1E-02 0 0
CUI: C1832855
Disease: CHOREOATHETOSIS/SPASTICITY, EPISODIC
CHOREOATHETOSIS/SPASTICITY, EPISODIC 		1 0 1 3.1E-02 0 0
CUI: C1835178
Disease: MACULAR DYSTROPHY, ATYPICAL VITELLIFORM
MACULAR DYSTROPHY, ATYPICAL VITELLIFORM 		1 0 1 3.1E-02 0 0
CUI: C1837206
Disease: Cryohydrocytosis, Stomatin-Deficient, with Mental Retardation, Seizures, Cataracts, and Massive Hepatosplenomegaly
Cryohydrocytosis, Stomatin-Deficient, with Mental Retardation, Seizures, Cataracts, and Massive Hepatosplenomegaly 		1 0 1 3.1E-02 0 0
CUI: C1842062
Disease: MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 1F
MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 1F 		1 0 1 3.1E-02 0 0
CUI: C1847507
Disease: Paroxysmal lethargy
Paroxysmal lethargy 		1 0 1 3.1E-02 0 0