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: C0154671
Disease: Degenerative brain disorder
Degenerative brain disorder 		16 0 1 6.2E-02 0 0
CUI: C0022340
Disease: Late-Infantile Neuronal Ceroid Lipfuscinosis
Late-Infantile Neuronal Ceroid Lipfuscinosis 		19 0 1 5.3E-02 0 0
CUI: C0393571
Disease: Multiple System Atrophy
Multiple System Atrophy 		19 0 1 5.3E-02 0 0
CUI: C0728829
Disease: Congenital pes cavus
Congenital pes cavus 		19 0 1 5.3E-02 0 0
CUI: C0751036
Disease: Hereditary Motor and Sensory Neuropathy Type I
Hereditary Motor and Sensory Neuropathy Type I 		19 84 1 5.3E-02 2 2.3E-02
CUI: C0338462
Disease: Semantic Dementia
Semantic Dementia 		20 0 1 5.0E-02 0 0
CUI: C0043020
Disease: Wallerian Degeneration
Wallerian Degeneration 		21 0 1 4.8E-02 0 0
CUI: C1408174
Disease: Hypertrophic neuropathy of infancy
Hypertrophic neuropathy of infancy 		21 0 1 4.8E-02 0 0
CUI: C1408182
Disease: Hereditary motor and sensory neuropathy, types I-IV
Hereditary motor and sensory neuropathy, types I-IV 		21 0 1 4.8E-02 0 0
CUI: C1843077
Disease: Segmental peripheral demyelination/remyelination
Segmental peripheral demyelination/remyelination 		21 0 1 4.8E-02 0 0
CUI: C2875300
Disease: Peroneal muscular atrophy (axonal type) (hypertrophic type)
Peroneal muscular atrophy (axonal type) (hypertrophic type) 		21 0 1 4.8E-02 0 0
CUI: C3890602
Disease: Bodily Pain
Bodily Pain 		22 0 1 4.5E-02 0 0
CUI: C1955760
Disease: Idiopathic normal pressure hydrocephalus (INPH)
Idiopathic normal pressure hydrocephalus (INPH) 		25 0 1 4.0E-02 0 0
CUI: C0205713
Disease: Roussy-Levy Syndrome (disorder)
Roussy-Levy Syndrome (disorder) 		26 0 1 3.8E-02 0 0
CUI: C0342200
Disease: Endemic Cretinism
Endemic Cretinism 		26 0 1 3.8E-02 0 0
CUI: C0878575
Disease: Peripheral demyelination
Peripheral demyelination 		27 0 1 3.7E-02 0 0
CUI: C1847906
Disease: Onion bulb formation
Onion bulb formation 		28 0 1 3.6E-02 0 0
CUI: C1858285
Disease: Decreased number of peripheral myelinated nerve fibers
Decreased number of peripheral myelinated nerve fibers 		28 0 1 3.6E-02 0 0
CUI: C0410203
Disease: X-linked centronuclear myopathy
X-linked centronuclear myopathy 		29 0 1 3.4E-02 0 0
CUI: C1852373
Disease: Mitochondrial encephalopathy
Mitochondrial encephalopathy 		32 0 1 3.1E-02 0 0
CUI: C0268407
Disease: Senile cardiac amyloidosis
Senile cardiac amyloidosis 		33 0 1 3.0E-02 0 0
CUI: C0393570
Disease: Corticobasal degeneration
Corticobasal degeneration 		35 0 1 2.9E-02 0 0
CUI: C3665464
Disease: Dementia due to Alzheimer's disease (disorder)
Dementia due to Alzheimer's disease (disorder) 		35 0 1 2.9E-02 0 0
CUI: C4011788
Disease: Behavioral variant of frontotemporal dementia
Behavioral variant of frontotemporal dementia 		35 0 1 2.9E-02 0 0
CUI: C4543926
Disease: Narcolepsy type 1
Narcolepsy type 1 		35 0 1 2.9E-02 0 0