Source: CURATED ×
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: C3151226
Disease: FICOLIN 3 DEFICIENCY
FICOLIN 3 DEFICIENCY 		1 0 1 4.3E-02 0 0
CUI: C3280642
Disease: Complement Component 4a Deficiency
Complement Component 4a Deficiency 		1 0 1 4.3E-02 0 0
CUI: C3541319
Disease: SHORT STATURE, OPTIC NERVE ATROPHY, AND PELGER-HUET ANOMALY
SHORT STATURE, OPTIC NERVE ATROPHY, AND PELGER-HUET ANOMALY 		1 0 1 4.3E-02 0 0
CUI: C3552553
Disease: HYPOGONADOTROPIC HYPOGONADISM 5 WITH OR WITHOUT ANOSMIA
HYPOGONADOTROPIC HYPOGONADISM 5 WITH OR WITHOUT ANOSMIA 		1 0 1 4.3E-02 0 0
CUI: C3554225
Disease: LEPTIN RECEPTOR DEFICIENCY
LEPTIN RECEPTOR DEFICIENCY 		1 0 1 4.3E-02 0 0
CUI: C3809651
Disease: INFANTILE LIVER FAILURE SYNDROME 2
INFANTILE LIVER FAILURE SYNDROME 2 		1 0 1 4.3E-02 0 0
CUI: C3810042
Disease: MACULAR DEGENERATION, AGE-RELATED, 15
MACULAR DEGENERATION, AGE-RELATED, 15 		1 0 1 4.3E-02 0 0
CUI: C3810127
Disease: IMMUNODEFICIENCY 18
IMMUNODEFICIENCY 18 		1 0 1 4.3E-02 0 0
CUI: C3810129
Disease: IMMUNODEFICIENCY 18, SCID VARIANT
IMMUNODEFICIENCY 18, SCID VARIANT 		1 0 1 4.3E-02 0 0
CUI: C4310768
Disease: AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 2
AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 2 		1 0 1 4.3E-02 0 0
CUI: C4551557
Disease: IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME 1
IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME 1 		1 0 1 4.3E-02 0 0
CUI: C4748257
Disease: BONE MARROW FAILURE SYNDROME 4
BONE MARROW FAILURE SYNDROME 4 		1 0 1 4.3E-02 0 0
CUI: C0005859
Disease: Bloom Syndrome
Bloom Syndrome 		2 0 1 4.2E-02 0 0
CUI: C0034152
Disease: Henoch-Schoenlein Purpura
Henoch-Schoenlein Purpura 		2 0 1 4.2E-02 0 0
CUI: C0042386
Disease: Vasculitis, Hemorrhagic
Vasculitis, Hemorrhagic 		2 0 1 4.2E-02 0 0
CUI: C0086922
Disease: Rheumatoid Purpura
Rheumatoid Purpura 		2 0 1 4.2E-02 0 0
CUI: C0162770
Disease: Right Ventricular Hypertrophy
Right Ventricular Hypertrophy 		2 0 1 4.2E-02 0 0
CUI: C0242461
Disease: Purpura, Nonthrombocytopenic
Purpura, Nonthrombocytopenic 		2 0 1 4.2E-02 0 0
CUI: C0265354
Disease: CHARGE Syndrome
CHARGE Syndrome 		2 0 1 4.2E-02 0 0
CUI: C0342788
Disease: Renal carnitine transport defect
Renal carnitine transport defect 		2 0 1 4.2E-02 0 0
CUI: C0376362
Disease: Purpura Hemorrhagica
Purpura Hemorrhagica 		2 0 1 4.2E-02 0 0
CUI: C0796113
Disease: Nephroblastomatosis, fetal ascites, macrosomia and Wilms tumor
Nephroblastomatosis, fetal ascites, macrosomia and Wilms tumor 		2 0 1 4.2E-02 0 0
CUI: C1834671
Disease: FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY 1B
FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY 1B 		2 0 1 4.2E-02 0 0
CUI: C2363142
Disease: T-Cell Prolymphocytic Leukemia
T-Cell Prolymphocytic Leukemia 		2 0 1 4.2E-02 0 0
CUI: C2936502
Disease: Familial CHARGE Syndrome
Familial CHARGE Syndrome 		2 0 1 4.2E-02 0 0