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: C0234649
Disease: Abnormal saccadic eye movement
Abnormal saccadic eye movement 		17 0 1 5.9E-02 0 0
CUI: C1854699
Disease: Diffuse cerebellar atrophy
Diffuse cerebellar atrophy 		17 0 1 5.9E-02 0 0
CUI: C4025660
Disease: Abnormality of the ankles
Abnormality of the ankles 		17 0 1 5.9E-02 0 0
CUI: C1833225
Disease: Dystrophic toenail
Dystrophic toenail 		18 0 1 5.6E-02 0 0
CUI: C0574002
Disease: Edema of foot (finding)
Edema of foot (finding) 		19 0 1 5.3E-02 0 0
CUI: C0699739
Disease: Sensory Neuropathy, Hereditary
Sensory Neuropathy, Hereditary 		19 0 1 5.3E-02 0 0
CUI: C4024921
Disease: Lower limb amyotrophy
Lower limb amyotrophy 		19 0 1 5.3E-02 0 0
CUI: C1857171
Disease: Episodic hyperhidrosis
Episodic hyperhidrosis 		20 0 1 5.0E-02 0 0
CUI: C0431370
Disease: Atrophy of corpus callosum
Atrophy of corpus callosum 		21 2 1 4.8E-02 1 2.6E-02
CUI: C1853761
Disease: SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 1
SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 1 		21 0 1 4.8E-02 0 0
CUI: C0162285
Disease: Edema of eyelid
Edema of eyelid 		22 0 1 4.5E-02 0 0
CUI: C0269269
Disease: Inversion of nipple (disorder)
Inversion of nipple (disorder) 		27 7 1 3.7E-02 1 2.3E-02
CUI: C0751602
Disease: Hereditary Autosomal Dominant Spastic Paraplegia
Hereditary Autosomal Dominant Spastic Paraplegia 		27 0 1 3.7E-02 0 0
CUI: C3551426
Disease: Dystrophic fingernails
Dystrophic fingernails 		27 0 1 3.7E-02 0 0
CUI: C4024900
Disease: Atrophy/Degeneration affecting the brainstem
Atrophy/Degeneration affecting the brainstem 		27 0 1 3.7E-02 0 0
CUI: C1843663
Disease: Urinary bladder sphincter dysfunction
Urinary bladder sphincter dysfunction 		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: C4082172
Disease: Porencephalic cyst
Porencephalic cyst 		28 0 1 3.6E-02 0 0
CUI: C0085996
Disease: Child Development Deviations
Child Development Deviations 		29 0 1 3.4E-02 0 0
CUI: C0259749
Disease: Autonomic neuropathy
Autonomic neuropathy 		29 0 1 3.4E-02 0 0
CUI: C0085997
Disease: Child Development Disorders, Specific
Child Development Disorders, Specific 		30 0 1 3.3E-02 0 0
CUI: C0013144
Disease: Drowsiness
Drowsiness 		31 0 1 3.2E-02 0 0
CUI: C0238651
Disease: Ankle clonus
Ankle clonus 		32 0 1 3.1E-02 0 0
CUI: C0742028
Disease: Cerebellar vermis atrophy
Cerebellar vermis atrophy 		32 0 1 3.1E-02 0 0
CUI: C1854465
Disease: TUBEROUS SCLEROSIS 1 (disorder)
TUBEROUS SCLEROSIS 1 (disorder) 		32 0 1 3.1E-02 0 0