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: C0000786
Disease: Spontaneous abortion
Spontaneous abortion
188 0 1 5.3E-03 0 0
CUI: C0152427
Disease: Polydactyly
Polydactyly
188 0 1 5.3E-03 0 0
CUI: C4722099
Disease: High grade glioma
High grade glioma
190 0 1 5.3E-03 0 0
CUI: C1387005
Disease: Penis agenesis
Penis agenesis
217 0 1 4.6E-03 0 0
CUI: C0262655
Disease: Recurrent urinary tract infection
Recurrent urinary tract infection
237 0 1 4.2E-03 0 0
CUI: C1861305
Disease: TARSAL-CARPAL COALITION SYNDROME
TARSAL-CARPAL COALITION SYNDROME
261 0 1 3.8E-03 0 0
CUI: C1850049
Disease: Clinodactyly of the 5th finger
Clinodactyly of the 5th finger
284 0 1 3.5E-03 0 0
CUI: C0221357
Disease: Brachydactyly
Brachydactyly
325 0 1 3.1E-03 0 0
CUI: C0302142
Disease: Deformity
Deformity
350 0 1 2.9E-03 0 0
CUI: C0848558
Disease: Hypospadias
Hypospadias
366 0 1 2.7E-03 0 0
CUI: C0019569
Disease: Hirschsprung Disease
Hirschsprung Disease
384 0 1 2.6E-03 0 0
CUI: C0023470
Disease: Myeloid Leukemia
Myeloid Leukemia
385 0 1 2.6E-03 0 0
CUI: C1739135
Disease: Progression of prostate cancer
Progression of prostate cancer
398 0 1 2.5E-03 0 0
CUI: C0018798
Disease: Congenital Heart Defects
Congenital Heart Defects
406 0 1 2.5E-03 0 0
CUI: C0018818
Disease: Ventricular Septal Defects
Ventricular Septal Defects
426 0 1 2.3E-03 0 0
CUI: C0024232
Disease: Lymphatic Metastasis
Lymphatic Metastasis
463 0 1 2.2E-03 0 0
CUI: C4721414
Disease: Mantle cell lymphoma
Mantle cell lymphoma
466 0 1 2.1E-03 0 0
CUI: C0042133
Disease: Uterine Fibroids
Uterine Fibroids
569 0 1 1.8E-03 0 0
CUI: C0424605
Disease: Developmental delay (disorder)
Developmental delay (disorder)
584 0 1 1.7E-03 0 0
CUI: C1565489
Disease: Renal Insufficiency
Renal Insufficiency
615 0 1 1.6E-03 0 0
Precursor T-Cell Lymphoblastic Leukemia-Lymphoma
644 0 1 1.6E-03 0 0
CUI: C0038379
Disease: Strabismus
Strabismus
716 0 1 1.4E-03 0 0
CUI: C0555198
Disease: Malignant Glioma
Malignant Glioma
724 0 1 1.4E-03 0 0
CUI: C0021051
Disease: Immunologic Deficiency Syndromes
Immunologic Deficiency Syndromes
973 0 1 1.0E-03 0 0
CUI: C0598766
Disease: Leukemogenesis
Leukemogenesis
996 0 1 1.0E-03 0 0