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: C0036659
Disease: Sensation Disorders
Sensation Disorders 		1 0 1 0.33 0 0
CUI: C0270712
Disease: Late cortical cerebellar atrophy
Late cortical cerebellar atrophy 		1 0 1 0.33 0 0
CUI: C0751497
Disease: Special Senses Disorders
Special Senses Disorders 		1 0 1 0.33 0 0
CUI: C1708341
Disease: Heavier Menses
Heavier Menses 		1 0 1 0.33 0 0
CUI: C1858804
Disease: Cerebellar Ataxia, Deafness, and Narcolepsy
Cerebellar Ataxia, Deafness, and Narcolepsy 		1 0 1 0.33 0 0
CUI: C3279885
Disease: Hereditary Sensory and Autonomic Neuropathy Type Ie
Hereditary Sensory and Autonomic Neuropathy Type Ie 		1 0 1 0.33 0 0
CUI: C3275447
Disease: Ogden syndrome
Ogden syndrome 		6 0 2 0.29 0 0
CUI: C0393520
Disease: Harding ataxia
Harding ataxia 		2 0 1 0.25 0 0
CUI: C1835854
Disease: DEAFNESS, AUTOSOMAL RECESSIVE 68
DEAFNESS, AUTOSOMAL RECESSIVE 68 		2 0 1 0.25 0 0
CUI: C1853250
Disease: SPINOCEREBELLAR ATAXIA 23
SPINOCEREBELLAR ATAXIA 23 		2 0 1 0.25 0 0
CUI: C4237239
Disease: Opioid use disorder, severe
Opioid use disorder, severe 		2 0 1 0.25 0 0
CUI: C4310780
Disease: SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 23
SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 23 		2 0 1 0.25 0 0
CUI: C0151583
Disease: Abnormality of the cerebrospinal fluid
Abnormality of the cerebrospinal fluid 		3 0 1 0.20 0 0
CUI: C1696082
Disease: Peritoneal Necrotic Lesion
Peritoneal Necrotic Lesion 		3 0 1 0.20 0 0
CUI: C4518339
Disease: Sporadic adult-onset ataxia of unknown etiology
Sporadic adult-onset ataxia of unknown etiology 		3 0 1 0.20 0 0
CUI: C4024941
Disease: Dilated third ventricle
Dilated third ventricle 		4 0 1 0.17 0 0
CUI: C0086405
Disease: Hereditary Sensory Radicular Neuropathy
Hereditary Sensory Radicular Neuropathy 		5 0 1 0.14 0 0
CUI: C0030200
Disease: Pain, Intractable
Pain, Intractable 		6 0 1 0.12 0 0
CUI: C0152027
Disease: Sensory Disorders
Sensory Disorders 		6 0 1 0.12 0 0
CUI: C1274795
Disease: Urban Schosser Spohn syndrome
Urban Schosser Spohn syndrome 		6 0 1 0.12 0 0
CUI: C1835228
Disease: Predominantly lower limb lymphedema
Predominantly lower limb lymphedema 		6 0 1 0.12 0 0
CUI: C0020075
Disease: Hereditary Sensory Autonomic Neuropathy, Type 5
Hereditary Sensory Autonomic Neuropathy, Type 5 		7 0 1 0.11 0 0
CUI: C0232766
Disease: Asterixis
Asterixis 		7 0 1 0.11 0 0
CUI: C0454606
Disease: Oral Dyskinesia
Oral Dyskinesia 		7 0 1 0.11 0 0
CUI: C0752196
Disease: Ballismus
Ballismus 		7 0 1 0.11 0 0