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: C1858479
Disease: Spastic paraplegia 11, autosomal recessive
Spastic paraplegia 11, autosomal recessive 		9 0 5 0.29 0 0
CUI: C1849115
Disease: SPASTIC PARAPLEGIA 5A, AUTOSOMAL RECESSIVE (disorder)
SPASTIC PARAPLEGIA 5A, AUTOSOMAL RECESSIVE (disorder) 		2 0 2 0.15 0 0
CUI: C3550973
Disease: NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 5
NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 5 		19 0 4 0.14 0 0
CUI: C0751603
Disease: Autosomal Recessive Hereditary Spastic Paraplegia
Autosomal Recessive Hereditary Spastic Paraplegia 		20 0 4 0.14 0 0
CUI: C2931845
Disease: Neurodegeneration with brain iron accumulation (NBIA)
Neurodegeneration with brain iron accumulation (NBIA) 		40 0 6 0.13 0 0
CUI: C1142448
Disease: Apraxia of eyelid
Apraxia of eyelid 		5 0 2 0.12 0 0
CUI: C1846564
Disease: SPASTIC PARAPLEGIA 7, AUTOSOMAL RECESSIVE
SPASTIC PARAPLEGIA 7, AUTOSOMAL RECESSIVE 		6 0 2 0.12 0 0
CUI: C0393556
Disease: Complicated hereditary spastic paraplegia
Complicated hereditary spastic paraplegia 		16 0 3 0.12 0 0
CUI: C0270724
Disease: Infantile Neuroaxonal Dystrophy
Infantile Neuroaxonal Dystrophy 		17 0 3 0.11 0 0
CUI: C0393555
Disease: Pure hereditary spastic paraplegia
Pure hereditary spastic paraplegia 		9 0 2 1.0E-01 0 0
CUI: C0393559
Disease: Troyer syndrome
Troyer syndrome 		9 0 2 1.0E-01 0 0
CUI: C1846017
Disease: Progressive pes cavus
Progressive pes cavus 		9 0 2 1.0E-01 0 0
CUI: C2748610
Disease: Progressive extrapyramidal movement disorder
Progressive extrapyramidal movement disorder 		9 0 2 1.0E-01 0 0
CUI: C1271100
Disease: Lower limb spasticity
Lower limb spasticity 		43 0 5 9.8E-02 0 0
CUI: C1846868
Disease: Parkinsonism with favorable response to dopaminergic medication
Parkinsonism with favorable response to dopaminergic medication 		21 0 3 9.7E-02 0 0
CUI: C1836843
Disease: Progressive inability to walk
Progressive inability to walk 		10 0 2 9.5E-02 0 0
CUI: C1866855
Disease: Spastic paraplegia 4, autosomal dominant
Spastic paraplegia 4, autosomal dominant 		10 0 2 9.5E-02 0 0
CUI: C0234517
Disease: Anarthria speech disorder
Anarthria speech disorder 		11 0 2 9.1E-02 0 0
CUI: C1868596
Disease: Atypical Parkinson Disease
Atypical Parkinson Disease 		11 0 2 9.1E-02 0 0
CUI: C0231698
Disease: Gait, Scissors
Gait, Scissors 		12 0 2 8.7E-02 0 0
CUI: C0431369
Disease: Dysgenesis of corpus callosum
Dysgenesis of corpus callosum 		25 0 3 8.6E-02 0 0
CUI: C0392678
Disease: Swallowing problem
Swallowing problem 		13 0 2 8.3E-02 0 0
CUI: C1389102
Disease: Atrophy of the spinal cord
Atrophy of the spinal cord 		13 0 2 8.3E-02 0 0
CUI: C0752105
Disease: Parkinsonism, Juvenile
Parkinsonism, Juvenile 		40 0 4 8.2E-02 0 0
CUI: C0751602
Disease: Hereditary Autosomal Dominant Spastic Paraplegia
Hereditary Autosomal Dominant Spastic Paraplegia 		27 0 3 8.1E-02 0 0