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: C0018944
Disease: Hematoma
Hematoma 		1 0 1 0.12 0 0
CUI: C0027665
Disease: Neoplasms, Nerve Tissue
Neoplasms, Nerve Tissue 		1 0 1 0.12 0 0
CUI: C0598121
Disease: Hypoglycorrhachia
Hypoglycorrhachia 		1 0 1 0.12 0 0
CUI: C1333067
Disease: Clear Cell Hepatocellular Carcinoma
Clear Cell Hepatocellular Carcinoma 		1 0 1 0.12 0 0
CUI: C1832855
Disease: CHOREOATHETOSIS/SPASTICITY, EPISODIC
CHOREOATHETOSIS/SPASTICITY, EPISODIC 		1 0 1 0.12 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 0.12 0 0
CUI: C1847507
Disease: Paroxysmal lethargy
Paroxysmal lethargy 		1 0 1 0.12 0 0
CUI: C3149117
Disease: GLUT1 DEFICIENCY SYNDROME 1, AUTOSOMAL RECESSIVE
GLUT1 DEFICIENCY SYNDROME 1, AUTOSOMAL RECESSIVE 		1 0 1 0.12 0 0
CUI: C3544265
Disease: Intrahepatic cholangiocarcinoma recurrent
Intrahepatic cholangiocarcinoma recurrent 		1 0 1 0.12 0 0
CUI: C3553859
Disease: EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 12
EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 12 		1 0 1 0.12 0 0
CUI: C3553958
Disease: METAPHYSEAL ENCHONDROMATOSIS WITH D-2-HYDROXYGLUTARIC ACIDURIA
METAPHYSEAL ENCHONDROMATOSIS WITH D-2-HYDROXYGLUTARIC ACIDURIA 		1 0 1 0.12 0 0
CUI: C4016231
Disease: GLIOBLASTOMA MULTIFORME, SOMATIC
GLIOBLASTOMA MULTIFORME, SOMATIC 		1 0 1 0.12 0 0
CUI: C4551966
Disease: GLUT1 DEFICIENCY SYNDROME 1
GLUT1 DEFICIENCY SYNDROME 1 		1 0 1 0.12 0 0
CUI: C0022079
Disease: Iris Neoplasms
Iris Neoplasms 		2 0 1 0.11 0 0
CUI: C0086626
Disease: Minamata Disease
Minamata Disease 		2 0 1 0.11 0 0
CUI: C0236964
Disease: Attention Deficit and Disruptive Behavior Disorders
Attention Deficit and Disruptive Behavior Disorders 		2 0 1 0.11 0 0
CUI: C0268497
Disease: Brown oculocutaneous albinism
Brown oculocutaneous albinism 		2 0 1 0.11 0 0
CUI: C0268503
Disease: Autosomal recessive ocular albinism
Autosomal recessive ocular albinism 		2 0 1 0.11 0 0
CUI: C0274859
Disease: Inorganic Mercury Poisoning
Inorganic Mercury Poisoning 		2 0 1 0.11 0 0
CUI: C0274860
Disease: Mercury Poisoning, Organic
Mercury Poisoning, Organic 		2 0 1 0.11 0 0
CUI: C0391870
Disease: Abnormality of red blood cells
Abnormality of red blood cells 		2 0 1 0.11 0 0
CUI: C0546384
Disease: Focal oral mucinosis
Focal oral mucinosis 		2 0 1 0.11 0 0
CUI: C0596773
Disease: Infectious Encephalitis
Infectious Encephalitis 		2 0 1 0.11 0 0
CUI: C0750968
Disease: Central Nervous System Metabolic Disorders
Central Nervous System Metabolic Disorders 		2 0 1 0.11 0 0
CUI: C0751743
Disease: Metabolic Disorder, Central Nervous System, Acquired
Metabolic Disorder, Central Nervous System, Acquired 		2 0 1 0.11 0 0