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: C0745109
Disease: Macular hyperpigmentation
Macular hyperpigmentation 		2 0 1 0.12 0 0
CUI: C0935560
Disease: Multiple disability
Multiple disability 		2 0 1 0.12 0 0
CUI: C1835916
Disease: AICARDI-GOUTIERES SYNDROME 3
AICARDI-GOUTIERES SYNDROME 3 		2 0 1 0.12 0 0
CUI: C2931662
Disease: Baraitser Brett Piesowicz syndrome
Baraitser Brett Piesowicz syndrome 		2 0 1 0.12 0 0
CUI: C4024759
Disease: Macular hypopigmentation
Macular hypopigmentation 		2 0 1 0.12 0 0
CUI: C4225427
Disease: SINGLETON-MERTEN SYNDROME 1
SINGLETON-MERTEN SYNDROME 1 		2 0 1 0.12 0 0
CUI: C1704356
Disease: Enchondroma
Enchondroma 		41 0 5 0.12 0 0
CUI: C0152084
Disease: Jaccoud's syndrome
Jaccoud's syndrome 		3 0 1 0.11 0 0
CUI: C0206744
Disease: T-Lymphocytopenia, Idiopathic CD4-Positive
T-Lymphocytopenia, Idiopathic CD4-Positive 		3 0 1 0.11 0 0
CUI: C0432185
Disease: Aplasia of muscle
Aplasia of muscle 		13 0 2 0.11 0 0
CUI: C1835912
Disease: AICARDI-GOUTIERES SYNDROME 4
AICARDI-GOUTIERES SYNDROME 4 		3 0 1 0.11 0 0
CUI: C1865361
Disease: SHORT STATURE, AUDITORY CANAL ATRESIA, MANDIBULAR HYPOPLASIA, SKELETAL ABNORMALITIES
SHORT STATURE, AUDITORY CANAL ATRESIA, MANDIBULAR HYPOPLASIA, SKELETAL ABNORMALITIES 		3 0 1 0.11 0 0
CUI: C3277688
Disease: Progressive forgetfulness
Progressive forgetfulness 		3 0 1 0.11 0 0
CUI: C4024895
Disease: Atrophy/Degeneration involving the caudate nucleus
Atrophy/Degeneration involving the caudate nucleus 		3 0 1 0.11 0 0
CUI: C4024917
Disease: Congenital encephalopathy
Congenital encephalopathy 		3 0 1 0.11 0 0
CUI: C4552243
Disease: Dyschromatosis
Dyschromatosis 		3 0 1 0.11 0 0
CUI: C0031887
Disease: Picornaviridae Infections
Picornaviridae Infections 		4 0 1 1.0E-01 0 0
CUI: C0202083
Disease: Immunoglobulin A measurement
Immunoglobulin A measurement 		4 0 1 1.0E-01 0 0
CUI: C3277687
Disease: Central nervous system degeneration
Central nervous system degeneration 		4 0 1 1.0E-01 0 0
CUI: C3711385
Disease: Deoxyguanosine Kinase Deficiency
Deoxyguanosine Kinase Deficiency 		4 0 1 1.0E-01 0 0
CUI: C3860213
Disease: Autoinflammatory disorder
Autoinflammatory disorder 		60 0 6 9.8E-02 0 0
CUI: C0040458
Disease: Unerupted tooth
Unerupted tooth 		5 0 1 9.1E-02 0 0
CUI: C0149614
Disease: Adnexal mass
Adnexal mass 		5 0 1 9.1E-02 0 0
CUI: C0233417
Disease: Poor concentration
Poor concentration 		5 0 1 9.1E-02 0 0
CUI: C0240897
Disease: Retinal exudates
Retinal exudates 		5 0 1 9.1E-02 0 0