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: C0852975
Disease: Congenital cerebellar ataxia
Congenital cerebellar ataxia
8 0 3 0.21 0 0
CUI: C0271902
Disease: Microcytic normochromic anemia
Microcytic normochromic anemia
1 0 1 0.11 0 0
CUI: C0394004
Disease: Congenital non-progressive ataxia
Congenital non-progressive ataxia
1 0 1 0.11 0 0
CUI: C0796205
Disease: SPINOCEREBELLAR ATAXIA, X-LINKED 1
SPINOCEREBELLAR ATAXIA, X-LINKED 1
1 0 1 0.11 0 0
CUI: C0810006
Disease: Acute cerebrovascular disease
Acute cerebrovascular disease
1 0 1 0.11 0 0
Pleural Epithelioid Hemangioendothelioma
1 0 1 0.11 0 0
CUI: C1832585
Disease: CEREBELLAR ATAXIA, CAYMAN TYPE
CEREBELLAR ATAXIA, CAYMAN TYPE
1 0 1 0.11 0 0
ANEMIA, SIDEROBLASTIC, AND SPINOCEREBELLAR ATAXIA
1 0 1 0.11 0 0
CUI: C1847725
Disease: SPINOCEREBELLAR ATAXIA 15
SPINOCEREBELLAR ATAXIA 15
1 0 1 0.11 0 0
CEREBELLAR ATAXIA, NONPROGRESSIVE, WITH MENTAL RETARDATION
1 0 1 0.11 0 0
SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 17
1 0 1 0.11 0 0
Abnormality of the distal phalanx of the thumb
1 0 1 0.11 0 0
CUI: C4039473
Disease: 3-methylglutaconic aciduria type 5
3-methylglutaconic aciduria type 5
1 0 1 0.11 0 0
CORPUS CALLOSUM, AGENESIS OF, WITH FACIAL ANOMALIES AND CEREBELLAR ATAXIA
1 0 1 0.11 0 0
CUI: C4274322
Disease: Spinocerebellar ataxia type 15/16
Spinocerebellar ataxia type 15/16
1 0 1 0.11 0 0
X-linked non progressive cerebellar ataxia
1 0 1 0.11 0 0
CUI: C0003132
Disease: Anoxic Encephalopathy
Anoxic Encephalopathy
2 0 1 1.0E-01 0 0
CUI: C0561843
Disease: Memory, Episodic
Memory, Episodic
2 0 1 1.0E-01 0 0
CUI: C0995195
Disease: Anoxia of brain
Anoxia of brain
2 0 1 1.0E-01 0 0
CUI: C1140716
Disease: Hypoxic Brain Damage
Hypoxic Brain Damage
2 0 1 1.0E-01 0 0
Aldosterone-Producing Adrenal Cortex Adenoma
2 0 1 1.0E-01 0 0
2,4-Dienoyl-CoA Reductase Deficiency
2 0 1 1.0E-01 0 0
CUI: C3551041
Disease: Short ear
Short ear
2 0 1 1.0E-01 0 0
CUI: C4015009
Disease: Decreased plasma free carnitine
Decreased plasma free carnitine
2 0 1 1.0E-01 0 0
CUI: C4024932
Disease: Bilateral basal ganglia lesions
Bilateral basal ganglia lesions
2 0 1 1.0E-01 0 0