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: C0037188
Disease: Sinoatrial Block
Sinoatrial Block 		1 0 1 3.3E-02 0 0
CUI: C0267494
Disease: Chilaiditi Syndrome
Chilaiditi Syndrome 		1 0 1 3.3E-02 0 0
CUI: C0270958
Disease: Kocher-Debre-Semelaigne syndrome
Kocher-Debre-Semelaigne syndrome 		1 0 1 3.3E-02 0 0
CUI: C0333062
Disease: Hernia sac
Hernia sac 		1 0 1 3.3E-02 0 0
CUI: C0410165
Disease: X-linked muscular dystrophy with abnormal dystrophin
X-linked muscular dystrophy with abnormal dystrophin 		1 0 1 3.3E-02 0 0
CUI: C0429803
Disease: Bladder trabeculation
Bladder trabeculation 		1 0 1 3.3E-02 0 0
CUI: C0495694
Disease: Dysarthria and anarthria
Dysarthria and anarthria 		1 0 1 3.3E-02 0 0
CUI: C0555197
Disease: Florid cemento-osseous dysplasia
Florid cemento-osseous dysplasia 		1 0 1 3.3E-02 0 0
CUI: C0699741
Disease: Benign congenital myopathy
Benign congenital myopathy 		1 0 1 3.3E-02 0 0
CUI: C0796031
Disease: Malouf syndrome
Malouf syndrome 		1 0 1 3.3E-02 0 0
CUI: C0796083
Disease: Najjar syndrome
Najjar syndrome 		1 0 1 3.3E-02 0 0
CUI: C1835380
Disease: Labial pseudohypertrophy
Labial pseudohypertrophy 		1 0 1 3.3E-02 0 0
CUI: C1835389
Disease: Increased intramuscular fat
Increased intramuscular fat 		1 0 1 3.3E-02 0 0
CUI: C1836050
Disease: Filaminopathy, autosomal dominant
Filaminopathy, autosomal dominant 		1 0 1 3.3E-02 0 0
CUI: C1836437
Disease: B-Cell Immunodeficiency, Distal Limb Anomalies, And Urogenital Malformations
B-Cell Immunodeficiency, Distal Limb Anomalies, And Urogenital Malformations 		1 0 1 3.3E-02 0 0
CUI: C1840365
Disease: King Denborough syndrome
King Denborough syndrome 		1 0 1 3.3E-02 0 0
CUI: C1843791
Disease: CARDIOMYOPATHY, DILATED, 1N
CARDIOMYOPATHY, DILATED, 1N 		1 0 1 3.3E-02 0 0
CUI: C1846010
Disease: URUGUAY FACIOCARDIOMUSCULOSKELETAL SYNDROME
URUGUAY FACIOCARDIOMUSCULOSKELETAL SYNDROME 		1 0 1 3.3E-02 0 0
CUI: C1847532
Disease: MYOPATHY, DISTAL, WITH ANTERIOR TIBIAL ONSET
MYOPATHY, DISTAL, WITH ANTERIOR TIBIAL ONSET 		1 0 1 3.3E-02 0 0
CUI: C1847902
Disease: CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE B (disorder)
CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE B (disorder) 		1 0 1 3.3E-02 0 0
CUI: C1848456
Disease: Atypical or prolonged hepatitis
Atypical or prolonged hepatitis 		1 0 1 3.3E-02 0 0
CUI: C1850709
Disease: Myopathy, Hyaline Body, Autosomal Recessive
Myopathy, Hyaline Body, Autosomal Recessive 		1 0 1 3.3E-02 0 0
CUI: C1857829
Disease: Heart-hand syndrome, Slovenian type
Heart-hand syndrome, Slovenian type 		1 0 1 3.3E-02 0 0
CUI: C1861753
Disease: Multiminicore Disease, Moderate, with Hand Involvement
Multiminicore Disease, Moderate, with Hand Involvement 		1 0 1 3.3E-02 0 0
CUI: C1862133
Disease: Decreased finger mobility
Decreased finger mobility 		1 0 1 3.3E-02 0 0