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: C0233558
Disease: Temper tantrum
Temper tantrum 		1 0 1 0.25 0 0
CUI: C0262525
Disease: Incomplete right bundle branch block
Incomplete right bundle branch block 		1 0 1 0.25 0 0
CUI: C0345203
Disease: Congenital atresia of large intestine
Congenital atresia of large intestine 		1 0 1 0.25 0 0
CUI: C0454649
Disease: Developmental syntactic impairment
Developmental syntactic impairment 		1 0 1 0.25 0 0
CUI: C0546965
Disease: Parachute malformation of mitral valve
Parachute malformation of mitral valve 		1 0 1 0.25 0 0
CUI: C0270710
Disease: Bing-Neel syndrome
Bing-Neel syndrome 		3 0 1 0.17 0 0
CUI: C0338986
Disease: Atypical autism
Atypical autism 		3 0 1 0.17 0 0
CUI: C1707400
Disease: Classic medulloblastoma
Classic medulloblastoma 		3 0 1 0.17 0 0
CUI: C1409792
Disease: Coronary sinus defect
Coronary sinus defect 		5 0 1 0.12 0 0
CUI: C1840283
Disease: ICHTHYOSIS--CHEEK--EYEBROW SYNDROME
ICHTHYOSIS--CHEEK--EYEBROW SYNDROME 		5 0 1 0.12 0 0
CUI: C4721769
Disease: Citrullinemia Type 1
Citrullinemia Type 1 		5 0 1 0.12 0 0
CUI: C0037789
Disease: Specific reading disorder
Specific reading disorder 		6 0 1 0.11 0 0
CUI: C0302826
Disease: Expressed Emotion
Expressed Emotion 		6 0 1 0.11 0 0
CUI: C3898765
Disease: Keratitis caused by infection
Keratitis caused by infection 		6 0 1 0.11 0 0
CUI: C4552213
Disease: Broad autism phenotype
Broad autism phenotype 		6 0 1 0.11 0 0
CUI: C0175683
Disease: Citrullinemia
Citrullinemia 		7 0 1 1.0E-01 0 0
CUI: C0795858
Disease: Chromosome 15q, trisomy
Chromosome 15q, trisomy 		7 0 1 1.0E-01 0 0
CUI: C1838579
Disease: Pseudobulbar signs
Pseudobulbar signs 		7 0 1 1.0E-01 0 0
CUI: C0231617
Disease: Catch - Finding of sensory dimension of pain
Catch - Finding of sensory dimension of pain 		8 0 1 9.1E-02 0 0
CUI: C0265326
Disease: Bannayan-Riley-Ruvalcaba Syndrome
Bannayan-Riley-Ruvalcaba Syndrome 		9 0 1 8.3E-02 0 0
CUI: C0268547
Disease: Argininosuccinic Aciduria
Argininosuccinic Aciduria 		9 0 1 8.3E-02 0 0
CUI: C3266843
Disease: 47, XYY syndrome
47, XYY syndrome 		9 0 1 8.3E-02 0 0
CUI: C1856113
Disease: Mowat-Wilson syndrome
Mowat-Wilson syndrome 		10 0 1 7.7E-02 0 0
CUI: C0024214
Disease: Lymphangiectasis
Lymphangiectasis 		11 0 1 7.1E-02 0 0
CUI: C0268548
Disease: Hyperargininemia
Hyperargininemia 		11 0 1 7.1E-02 0 0