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: C0242036
Disease: Paraplegia, Ataxic
Paraplegia, Ataxic 		1 0 1 0.33 0 0
CUI: C0278114
Disease: Paraplegia, Cerebral
Paraplegia, Cerebral 		1 0 1 0.33 0 0
CUI: C0278115
Disease: Paraplegia, Spinal
Paraplegia, Spinal 		1 0 1 0.33 0 0
CUI: C0452143
Disease: Paraplegia, Flaccid
Paraplegia, Flaccid 		1 0 1 0.33 0 0
CUI: C1968845
Disease: Primary Lateral Sclerosis, Adult, 1
Primary Lateral Sclerosis, Adult, 1 		1 0 1 0.33 0 0
CUI: C1969796
Disease: ATAXIA, SPASTIC, 2, AUTOSOMAL RECESSIVE (disorder)
ATAXIA, SPASTIC, 2, AUTOSOMAL RECESSIVE (disorder) 		1 0 1 0.33 0 0
CUI: C2750784
Disease: SPASTIC PARAPLEGIA 44, AUTOSOMAL RECESSIVE (disorder)
SPASTIC PARAPLEGIA 44, AUTOSOMAL RECESSIVE (disorder) 		1 0 1 0.33 0 0
CUI: C4024175
Disease: Cerebellar ataxia associated with quadrupedal gait
Cerebellar ataxia associated with quadrupedal gait 		1 1 1 0.33 1 0.33
CUI: C4747646
Disease: LYMPHATIC MALFORMATION 3
LYMPHATIC MALFORMATION 3 		1 0 1 0.33 0 0
CUI: C0742191
Disease: Cervical spinal cord atrophy
Cervical spinal cord atrophy 		2 0 1 0.25 0 0
CUI: C1608410
Disease: Head titubation
Head titubation 		7 0 2 0.25 0 0
CUI: C1969462
Disease: Demyelinating motor neuropathy
Demyelinating motor neuropathy 		2 0 1 0.25 0 0
CUI: C4749302
Disease: Maternal uniparental disomy of chromosome 1
Maternal uniparental disomy of chromosome 1 		2 0 1 0.25 0 0
CUI: C1832597
Disease: Herniation of intervertebral nuclei
Herniation of intervertebral nuclei 		3 2 1 0.20 1 0.25
CUI: C4476727
Disease: Erratic myoclonus
Erratic myoclonus 		3 0 1 0.20 0 0
CUI: C0017563
Disease: Gingival Diseases
Gingival Diseases 		4 0 1 0.17 0 0
CUI: C0235439
Disease: Ankle edema (finding)
Ankle edema (finding) 		4 0 1 0.17 0 0
CUI: C1837355
Disease: Leukodystrophy, Hypomyelinating, 2
Leukodystrophy, Hypomyelinating, 2 		4 14 1 0.17 1 6.2E-02
CUI: C1850303
Disease: PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL RECESSIVE
PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL RECESSIVE 		4 0 1 0.17 0 0
CUI: C1853249
Disease: SPINOCEREBELLAR ATAXIA 28
SPINOCEREBELLAR ATAXIA 28 		4 0 1 0.17 0 0
CUI: C4021577
Disease: Abnormality of somatosensory evoked potentials
Abnormality of somatosensory evoked potentials 		4 0 1 0.17 0 0
CUI: C4022687
Disease: Abnormal motor evoked potentials
Abnormal motor evoked potentials 		4 0 1 0.17 0 0
CUI: C0231690
Disease: Titubation
Titubation 		5 0 1 0.14 0 0
CUI: C3711370
Disease: Spastic Paraplegia Type 7
Spastic Paraplegia Type 7 		5 2 1 0.14 1 0.25
CUI: C4024929
Disease: Slowed slurred speech
Slowed slurred speech 		5 0 1 0.14 0 0