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: C0019295
Disease: Inguinal Hernia, Direct
Inguinal Hernia, Direct 		1 0 1 7.7E-02 0 0
CUI: C1860896
Disease: COLORECTAL CANCER, HEREDITARY NONPOLYPOSIS, TYPE 6
COLORECTAL CANCER, HEREDITARY NONPOLYPOSIS, TYPE 6 		1 0 1 7.7E-02 0 0
CUI: C1862683
Disease: Townes-Brocks-Branchiootorenal-Like Syndrome
Townes-Brocks-Branchiootorenal-Like Syndrome 		1 0 1 7.7E-02 0 0
CUI: C1862693
Disease: Pseudoepiphyses of second metacarpal
Pseudoepiphyses of second metacarpal 		1 0 1 7.7E-02 0 0
CUI: C1969404
Disease: Prominent frontal sinuses
Prominent frontal sinuses 		1 0 1 7.7E-02 0 0
CUI: C1969410
Disease: Bidirectional ventricular ectopy
Bidirectional ventricular ectopy 		1 0 1 7.7E-02 0 0
CUI: C2674574
Disease: Aortic aneurysm, familial thoracic 3
Aortic aneurysm, familial thoracic 3 		1 0 1 7.7E-02 0 0
CUI: C2697933
Disease: Loeys-Dietz Syndrome Type 1
Loeys-Dietz Syndrome Type 1 		1 0 1 7.7E-02 0 0
CUI: C3151431
Disease: ATRIAL FIBRILLATION, FAMILIAL, 9
ATRIAL FIBRILLATION, FAMILIAL, 9 		1 0 1 7.7E-02 0 0
CUI: C3280452
Disease: SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 12
SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 12 		1 0 1 7.7E-02 0 0
CUI: C3550903
Disease: CORNELIA DE LANGE SYNDROME 5
CORNELIA DE LANGE SYNDROME 5 		1 0 1 7.7E-02 0 0
CUI: C4015519
Disease: EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 28
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 28 		1 0 1 7.7E-02 0 0
CUI: C4021236
Disease: 2-4 finger syndactyly
2-4 finger syndactyly 		1 0 1 7.7E-02 0 0
CUI: C4023465
Disease: EEG with occipital slowing
EEG with occipital slowing 		1 1 1 7.7E-02 1 0.25
CUI: C4048833
Disease: Satyr ear
Satyr ear 		1 0 1 7.7E-02 0 0
CUI: C4073265
Disease: Abnormality of inferior oblique extraocular muscle
Abnormality of inferior oblique extraocular muscle 		1 1 1 7.7E-02 1 0.25
CUI: C4540324
Disease: MENTAL RETARDATION, AUTOSOMAL DOMINANT 49
MENTAL RETARDATION, AUTOSOMAL DOMINANT 49 		1 0 1 7.7E-02 0 0
CUI: C4551481
Disease: TOWNES-BROCKS SYNDROME 1
TOWNES-BROCKS SYNDROME 1 		1 0 1 7.7E-02 0 0
CUI: C4703491
Disease: Abnormal ear morphology
Abnormal ear morphology 		1 0 1 7.7E-02 0 0
CUI: C4706556
Disease: Hypotonia, speech impairment, severe cognitive delay syndrome
Hypotonia, speech impairment, severe cognitive delay syndrome 		1 0 1 7.7E-02 0 0
CUI: C4706702
Disease: Aneurysm of left subclavian artery
Aneurysm of left subclavian artery 		1 0 1 7.7E-02 0 0
CUI: C4747891
Disease: GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 17
GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 17 		1 0 1 7.7E-02 0 0
CUI: C4749578
Disease: Autosomal recessive cerebellar ataxia, epilepsy, intellectual disability syndrome due to WWOX deficiency
Autosomal recessive cerebellar ataxia, epilepsy, intellectual disability syndrome due to WWOX deficiency 		1 0 1 7.7E-02 0 0
CUI: C0026069
Disease: Middle Lobe Syndrome
Middle Lobe Syndrome 		2 0 1 7.1E-02 0 0
CUI: C0240880
Disease: Rectoperineal fistula
Rectoperineal fistula 		2 0 1 7.1E-02 0 0