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: C0003756
Disease: Arenaviridae Infections
Arenaviridae Infections 		1 0 1 4.8E-02 0 0
CUI: C0152072
Disease: Ovale malaria
Ovale malaria 		1 0 1 4.8E-02 0 0
CUI: C0155833
Disease: Hyperplasia of adenoids
Hyperplasia of adenoids 		1 0 1 4.8E-02 0 0
CUI: C0233643
Disease: Incoherent thinking
Incoherent thinking 		1 0 1 4.8E-02 0 0
CUI: C0271905
Disease: Acquired methemoglobinemia
Acquired methemoglobinemia 		1 0 1 4.8E-02 0 0
CUI: C0272132
Disease: Drug-induced hemolytic anemia
Drug-induced hemolytic anemia 		1 0 1 4.8E-02 0 0
CUI: C0339697
Disease: Congenital color blindness
Congenital color blindness 		1 0 1 4.8E-02 0 0
CUI: C0598121
Disease: Hypoglycorrhachia
Hypoglycorrhachia 		1 0 1 4.8E-02 0 0
CUI: C0746365
Disease: malaria relapse
malaria relapse 		1 0 1 4.8E-02 0 0
CUI: C0748726
Disease: Allergic sinusitis
Allergic sinusitis 		1 0 1 4.8E-02 0 0
CUI: C0865236
Disease: Acute intravascular hemolysis
Acute intravascular hemolysis 		1 0 1 4.8E-02 0 0
CUI: C1266156
Disease: Multicystic mesothelioma, benign
Multicystic mesothelioma, benign 		1 0 1 4.8E-02 0 0
CUI: C1275128
Disease: Autosomal recessive hyperimmunoglobulin M syndrome
Autosomal recessive hyperimmunoglobulin M syndrome 		1 0 1 4.8E-02 0 0
CUI: C1292231
Disease: In(Lu) phenotype (finding)
In(Lu) phenotype (finding) 		1 0 1 4.8E-02 0 0
CUI: C1832168
Disease: BLOOD GROUP--FROESE
BLOOD GROUP--FROESE 		1 0 1 4.8E-02 0 0
CUI: C1832855
Disease: CHOREOATHETOSIS/SPASTICITY, EPISODIC
CHOREOATHETOSIS/SPASTICITY, EPISODIC 		1 0 1 4.8E-02 0 0
CUI: C1837206
Disease: Cryohydrocytosis, Stomatin-Deficient, with Mental Retardation, Seizures, Cataracts, and Massive Hepatosplenomegaly
Cryohydrocytosis, Stomatin-Deficient, with Mental Retardation, Seizures, Cataracts, and Massive Hepatosplenomegaly 		1 0 1 4.8E-02 0 0
CUI: C1843042
Disease: Craniolenticulosutural Dysplasia
Craniolenticulosutural Dysplasia 		1 0 1 4.8E-02 0 0
CUI: C1844671
Disease: Dermoids of cornea
Dermoids of cornea 		1 0 1 4.8E-02 0 0
CUI: C1847507
Disease: Paroxysmal lethargy
Paroxysmal lethargy 		1 0 1 4.8E-02 0 0
CUI: C1862190
Disease: BLOOD GROUP--WRIGHT ANTIGEN
BLOOD GROUP--WRIGHT ANTIGEN 		1 0 1 4.8E-02 0 0
CUI: C1862191
Disease: BLOOD GROUP--WALDNER TYPE
BLOOD GROUP--WALDNER TYPE 		1 0 1 4.8E-02 0 0
CUI: C1868355
Disease: 6-Phosphogluconolactonase Deficiency
6-Phosphogluconolactonase Deficiency 		1 0 1 4.8E-02 0 0
CUI: C1969039
Disease: Renal Tubular Acidosis, Distal, With Normal Red Cell Morphology
Renal Tubular Acidosis, Distal, With Normal Red Cell Morphology 		1 0 1 4.8E-02 0 0
CUI: C1969673
Disease: Forehead hyperpigmentation
Forehead hyperpigmentation 		1 0 1 4.8E-02 0 0