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: C0003708
Disease: Arachnoiditis
Arachnoiditis
1 0 1 1.0E-02 0 0
CUI: C0006897
Disease: Capillariasis
Capillariasis
1 0 1 1.0E-02 0 0
CUI: C0007871
Disease: Uterine Cervical Incompetence
Uterine Cervical Incompetence
1 0 1 1.0E-02 0 0
CUI: C0020413
Disease: Hymenolepiasis
Hymenolepiasis
1 0 1 1.0E-02 0 0
CUI: C0024950
Disease: Maxillary Diseases
Maxillary Diseases
1 0 1 1.0E-02 0 0
CUI: C0029437
Disease: Idiopathic Multicentric Osteolyses
Idiopathic Multicentric Osteolyses
1 0 1 1.0E-02 0 0
CUI: C0150841
Disease: muscle pain or weakness
muscle pain or weakness
1 0 1 1.0E-02 0 0
CUI: C0152073
Disease: Taenia saginata infection
Taenia saginata infection
1 0 1 1.0E-02 0 0
Chronic myeloid leukemia in remission
1 0 1 1.0E-02 0 0
CUI: C0155100
Disease: Peripheral opacity of cornea
Peripheral opacity of cornea
1 0 1 1.0E-02 0 0
CUI: C0231450
Disease: Abnormal extension
Abnormal extension
1 0 1 1.0E-02 0 0
CUI: C0233283
Disease: Complete breech presentation
Complete breech presentation
1 0 1 1.0E-02 0 0
CUI: C0238590
Disease: Acrogeria
Acrogeria
1 0 1 1.0E-02 0 0
CUI: C0265856
Disease: Hypoplasia of right heart
Hypoplasia of right heart
1 0 1 1.0E-02 0 0
CUI: C0265974
Disease: Birthmark
Birthmark
1 0 1 1.0E-02 0 0
CUI: C0266062
Disease: Posterior open bite
Posterior open bite
1 0 1 1.0E-02 0 0
CUI: C0266094
Disease: Congenital macrocheilia
Congenital macrocheilia
1 0 1 1.0E-02 0 0
CUI: C0267024
Disease: Hypertrophy of lip
Hypertrophy of lip
1 0 1 1.0E-02 0 0
CUI: C0271616
Disease: Precocious female puberty
Precocious female puberty
1 0 1 1.0E-02 0 0
CUI: C0282643
Disease: Smith-Lemli-Opitz Syndrome, Type I
Smith-Lemli-Opitz Syndrome, Type I
1 0 1 1.0E-02 0 0
CUI: C0282644
Disease: Smith-Lemli-Opitz Syndrome, Type II
Smith-Lemli-Opitz Syndrome, Type II
1 0 1 1.0E-02 0 0
CUI: C0311343
Disease: Membranous conjunctivitis
Membranous conjunctivitis
1 0 1 1.0E-02 0 0
CUI: C0332885
Disease: Congenital stenosis
Congenital stenosis
1 0 1 1.0E-02 0 0
CUI: C0332972
Disease: Congenital vascular proliferation
Congenital vascular proliferation
1 0 1 1.0E-02 0 0
CUI: C0338562
Disease: Sciatic nerve compression
Sciatic nerve compression
1 0 1 1.0E-02 0 0