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: C0023138
Disease: Laurence-Moon Syndrome
Laurence-Moon Syndrome 		1 0 1 4.8E-02 0 0
CUI: C0037050
Disease: Sick Building Syndrome
Sick Building Syndrome 		1 0 1 4.8E-02 0 0
CUI: C0267548
Disease: Ileocolic intussusception
Ileocolic intussusception 		1 0 1 4.8E-02 0 0
CUI: C0333062
Disease: Hernia sac
Hernia sac 		1 0 1 4.8E-02 0 0
CUI: C0333814
Disease: Pappenheimer body (morphologic abnormality)
Pappenheimer body (morphologic abnormality) 		1 0 1 4.8E-02 0 0
CUI: C1833699
Disease: Osteopoikilosis, Isolated
Osteopoikilosis, Isolated 		1 0 1 4.8E-02 0 0
CUI: C1835093
Disease: Masticatory Muscles, Hypertrophy of
Masticatory Muscles, Hypertrophy of 		1 0 1 4.8E-02 0 0
CUI: C1836447
Disease: Nemaline myopathy 4
Nemaline myopathy 4 		1 0 1 4.8E-02 0 0
CUI: C1836448
Disease: Nemaline myopathy 1
Nemaline myopathy 1 		1 0 1 4.8E-02 0 0
CUI: C1836472
Disease: Nemaline myopathy 6
Nemaline myopathy 6 		1 0 1 4.8E-02 0 0
CUI: C1847667
Disease: CARDIOMYOPATHY, DILATED, 1L
CARDIOMYOPATHY, DILATED, 1L 		1 0 1 4.8E-02 0 0
CUI: C1850709
Disease: Myopathy, Hyaline Body, Autosomal Recessive
Myopathy, Hyaline Body, Autosomal Recessive 		1 0 1 4.8E-02 0 0
CUI: C1859093
Disease: Chorioretinal Dystrophy, Spinocerebellar Ataxia, and Hypogonadotropic Hypogonadism
Chorioretinal Dystrophy, Spinocerebellar Ataxia, and Hypogonadotropic Hypogonadism 		1 0 1 4.8E-02 0 0
CUI: C2219809
Disease: Generalized muscle wasting
Generalized muscle wasting 		1 0 1 4.8E-02 0 0
CUI: C2673482
Disease: Increased susceptibility to schizophrenia
Increased susceptibility to schizophrenia 		1 0 1 4.8E-02 0 0
CUI: C2677586
Disease: Spastic Paraplegia 39, Autosomal Recessive
Spastic Paraplegia 39, Autosomal Recessive 		1 0 1 4.8E-02 0 0
CUI: C2698740
Disease: Pappenheimer Body Count (lab procedure)
Pappenheimer Body Count (lab procedure) 		1 0 1 4.8E-02 0 0
CUI: C2750413
Disease: Cap Myopathy, Tpm2-Related
Cap Myopathy, Tpm2-Related 		1 0 1 4.8E-02 0 0
CUI: C2750414
Disease: CAP MYOPATHY, TPM3-RELATED (disorder)
CAP MYOPATHY, TPM3-RELATED (disorder) 		1 0 1 4.8E-02 0 0
CUI: C2750536
Disease: Nemaline Myopathy 3, With Intranuclear Rods
Nemaline Myopathy 3, With Intranuclear Rods 		1 0 1 4.8E-02 0 0
CUI: C2750537
Disease: Myopathy, Actin, Congenital, With Cores
Myopathy, Actin, Congenital, With Cores 		1 0 1 4.8E-02 0 0
CUI: C2931111
Disease: Myopia, susceptibility to
Myopia, susceptibility to 		1 0 1 4.8E-02 0 0
CUI: C2931505
Disease: Mixed sclerosing bone dystrophy
Mixed sclerosing bone dystrophy 		1 0 1 4.8E-02 0 0
CUI: C2936171
Disease: Familial Ebstein's Anomaly
Familial Ebstein's Anomaly 		1 0 1 4.8E-02 0 0
CUI: C3149399
Disease: DERMATOFIBROSIS LENTICULARIS DISSEMINATA, ISOLATED
DERMATOFIBROSIS LENTICULARIS DISSEMINATA, ISOLATED 		1 0 1 4.8E-02 0 0