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: C0037773
Disease: Spastic Paraplegia, Hereditary
Spastic Paraplegia, Hereditary 		123 41 67 0.34 8 6.3E-02
CUI: C1858712
Disease: Spastic paraplegia 10, autosomal dominant
Spastic paraplegia 10, autosomal dominant 		16 10 9 6.0E-02 5 5.1E-02
CUI: C0034152
Disease: Henoch-Schoenlein Purpura
Henoch-Schoenlein Purpura 		198 59 51 0.18 7 4.8E-02
CUI: C1849115
Disease: SPASTIC PARAPLEGIA 5A, AUTOSOMAL RECESSIVE (disorder)
SPASTIC PARAPLEGIA 5A, AUTOSOMAL RECESSIVE (disorder) 		2 16 2 1.4E-02 5 4.8E-02
CUI: C1849128
Disease: Spastic paraplegia 15, autosomal recessive
Spastic paraplegia 15, autosomal recessive 		3 46 3 2.1E-02 6 4.5E-02
CUI: C0013362
Disease: Dysarthria
Dysarthria 		487 54 48 8.2E-02 4 2.8E-02
CUI: C0037771
Disease: Paraparesis, Spastic
Paraparesis, Spastic 		75 37 33 0.18 3 2.4E-02
CUI: C0027765
Disease: nervous system disorder
nervous system disorder 		977 39 44 4.1E-02 3 2.3E-02
CUI: C0010709
Disease: Cyst
Cyst 		221 6 5 1.4E-02 2 2.1E-02
CUI: C0751602
Disease: Hereditary Autosomal Dominant Spastic Paraplegia
Hereditary Autosomal Dominant Spastic Paraplegia 		27 7 16 0.10 2 2.0E-02
CUI: C3539507
Disease: SPASTIC PARAPLEGIA 56, AUTOSOMAL RECESSIVE
SPASTIC PARAPLEGIA 56, AUTOSOMAL RECESSIVE 		2 8 2 1.4E-02 2 2.0E-02
CUI: C0231687
Disease: Spastic gait
Spastic gait 		62 9 42 0.26 2 2.0E-02
CUI: C0795953
Disease: MASA SYNDROME (disorder)
MASA SYNDROME (disorder) 		16 13 10 6.7E-02 2 1.9E-02
CUI: C1853247
Disease: SPASTIC PARAPLEGIA 31, AUTOSOMAL DOMINANT
SPASTIC PARAPLEGIA 31, AUTOSOMAL DOMINANT 		2 13 2 1.4E-02 2 1.9E-02
CUI: C4551583
Disease: Cerebral cortical atrophy
Cerebral cortical atrophy 		271 13 25 6.4E-02 2 1.9E-02
CUI: C0751837
Disease: Gait Ataxia
Gait Ataxia 		172 17 14 4.6E-02 2 1.9E-02
CUI: C1849140
Disease: SPASTIC ATAXIA, CHARLEVOIX-SAGUENAY TYPE
SPASTIC ATAXIA, CHARLEVOIX-SAGUENAY TYPE 		23 240 4 2.5E-02 6 1.8E-02
CUI: C2931355
Disease: Spastic paraplegia 3, autosomal dominant
Spastic paraplegia 3, autosomal dominant 		3 18 3 2.1E-02 2 1.8E-02
CUI: C0575081
Disease: Gait abnormality
Gait abnormality 		312 23 37 8.8E-02 2 1.8E-02
CUI: C0265216
Disease: X-linked hydrocephalus syndrome
X-linked hydrocephalus syndrome 		20 24 7 4.5E-02 2 1.7E-02
CUI: C1842364
Disease: Central hypotonia
Central hypotonia 		50 25 5 2.6E-02 2 1.7E-02
CUI: C0023520
Disease: Leukodystrophy
Leukodystrophy 		190 27 22 7.1E-02 2 1.7E-02
CUI: C1846564
Disease: SPASTIC PARAPLEGIA 7, AUTOSOMAL RECESSIVE
SPASTIC PARAPLEGIA 7, AUTOSOMAL RECESSIVE 		6 38 5 3.4E-02 2 1.6E-02
CUI: C0424605
Disease: Developmental delay (disorder)
Developmental delay (disorder) 		584 68 21 3.0E-02 2 1.3E-02
CUI: C0239831
Disease: Hand muscle weakness
Hand muscle weakness 		14 1 4 2.6E-02 1 1.1E-02