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: C0018784
Disease: Sensorineural Hearing Loss (disorder)
Sensorineural Hearing Loss (disorder) 		783 111 7 8.8E-03 1 7.8E-03
CUI: C1861453
Disease: Pseudohyperkalemia Cardiff
Pseudohyperkalemia Cardiff 		218 60 1 4.2E-03 1 1.3E-02
CUI: C0002878
Disease: Anemia, Hemolytic
Anemia, Hemolytic 		154 31 1 5.7E-03 2 4.3E-02
CUI: C1970028
Disease: MALARIA, SUSCEPTIBILITY TO (finding)
MALARIA, SUSCEPTIBILITY TO (finding) 		5 23 1 3.7E-02 1 2.5E-02
CUI: C2675212
Disease: Spherocytosis, Type 4
Spherocytosis, Type 4 		1 23 1 4.3E-02 1 2.5E-02
CUI: C0019214
Disease: Hepatosplenomegaly
Hepatosplenomegaly 		127 21 3 2.0E-02 1 2.6E-02
CUI: C0039730
Disease: Thalassemia
Thalassemia 		136 18 1 6.3E-03 1 2.9E-02
CUI: C0037889
Disease: Hereditary spherocytosis
Hereditary spherocytosis 		53 13 5 7.0E-02 1 3.3E-02
CUI: C1864498
Disease: RENAL TUBULAR ACIDOSIS, DISTAL, AUTOSOMAL RECESSIVE
RENAL TUBULAR ACIDOSIS, DISTAL, AUTOSOMAL RECESSIVE 		5 13 5 0.22 2 6.9E-02
CUI: C1969038
Disease: RENAL TUBULAR ACIDOSIS, DISTAL, WITH HEMOLYTIC ANEMIA (disorder)
RENAL TUBULAR ACIDOSIS, DISTAL, WITH HEMOLYTIC ANEMIA (disorder) 		2 9 2 8.7E-02 7 0.35
CUI: C1862322
Disease: Ovalocytosis, Malaysian-Melanesian-Filipino Type
Ovalocytosis, Malaysian-Melanesian-Filipino Type 		9 5 2 6.7E-02 4 0.21
CUI: C2750771
Disease: Amelogenesis Imperfecta, Hypomaturation Type, Iia3
Amelogenesis Imperfecta, Hypomaturation Type, Iia3 		1 5 1 4.3E-02 1 4.5E-02
CUI: C1832168
Disease: BLOOD GROUP--FROESE
BLOOD GROUP--FROESE 		1 2 1 4.3E-02 1 5.3E-02
CUI: C1862190
Disease: BLOOD GROUP--WRIGHT ANTIGEN
BLOOD GROUP--WRIGHT ANTIGEN 		1 2 1 4.3E-02 1 5.3E-02
CUI: C1862191
Disease: BLOOD GROUP--WALDNER TYPE
BLOOD GROUP--WALDNER TYPE 		1 2 1 4.3E-02 1 5.3E-02
CUI: C3841459
Disease: Hb H disease
Hb H disease 		10 2 1 3.1E-02 2 0.11
CUI: C1969039
Disease: Renal Tubular Acidosis, Distal, With Normal Red Cell Morphology
Renal Tubular Acidosis, Distal, With Normal Red Cell Morphology 		1 1 1 4.3E-02 1 5.6E-02
CUI: C4015898
Disease: RENAL TUBULAR ACIDOSIS, AUTOSOMAL DOMINANT
RENAL TUBULAR ACIDOSIS, AUTOSOMAL DOMINANT 		1 1 1 4.3E-02 1 5.6E-02
CUI: C0000731
Disease: Abdomen distended
Abdomen distended 		103 0 2 1.6E-02 0 0
CUI: C0000737
Disease: Abdominal Pain
Abdominal Pain 		302 0 1 3.1E-03 0 0
CUI: C0000768
Disease: Congenital Abnormality
Congenital Abnormality 		1098 0 5 4.5E-03 0 0
CUI: C0000772
Disease: Multiple congenital anomalies
Multiple congenital anomalies 		251 0 3 1.1E-02 0 0
CUI: C0000786
Disease: Spontaneous abortion
Spontaneous abortion 		188 0 1 4.8E-03 0 0
CUI: C0000833
Disease: Abscess
Abscess 		96 0 1 8.5E-03 0 0
CUI: C0000846
Disease: Agenesis
Agenesis 		161 0 1 5.5E-03 0 0