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: C3711371
Disease: Spastic Paraplegia Type 4
Spastic Paraplegia Type 4
7 0 6 0.55 0 0
Spastic paraplegia 3, autosomal dominant
3 0 3 0.30 0 0
SPASTIC PARAPLEGIA 6, AUTOSOMAL DOMINANT (disorder)
2 0 2 0.20 0 0
SPASTIC PARAPLEGIA 31, AUTOSOMAL DOMINANT
2 0 2 0.20 0 0
CUI: C1504405
Disease: Pyramidal Tract Dysfunction
Pyramidal Tract Dysfunction
3 0 2 0.18 0 0
Spastic paraplegia 15, autosomal recessive
3 0 2 0.18 0 0
SPASTIC PARAPLEGIA 45, AUTOSOMAL RECESSIVE
3 0 2 0.18 0 0
Hereditary Autosomal Dominant Spastic Paraplegia
27 7 5 0.16 2 1.9E-02
Degeneration of the lateral corticospinal tracts
21 0 4 0.15 0 0
SPASTIC PARAPLEGIA 7, AUTOSOMAL RECESSIVE
6 0 2 0.14 0 0
CUI: C1864715
Disease: Thenar muscle atrophy
Thenar muscle atrophy
7 0 2 0.13 0 0
Spastic paraplegia 10, autosomal dominant
16 0 3 0.13 0 0
CUI: C0393555
Disease: Pure hereditary spastic paraplegia
Pure hereditary spastic paraplegia
9 0 2 0.12 0 0
Urinary bladder sphincter dysfunction
28 0 4 0.12 0 0
CUI: C0085606
Disease: Urgency of micturition
Urgency of micturition
40 0 5 0.11 0 0
CUI: C0238651
Disease: Ankle clonus
Ankle clonus
32 0 4 0.11 0 0
CUI: C1843570
Disease: Tip-toe gait
Tip-toe gait
11 1 2 0.11 1 9.9E-03
CUI: C0037932
Disease: Curvature of spine
Curvature of spine
1 0 1 1.0E-01 0 0
CUI: C0270804
Disease: Spastic Diplegia Cerebral Palsy
Spastic Diplegia Cerebral Palsy
1 0 1 1.0E-01 0 0
CUI: C0495694
Disease: Dysarthria and anarthria
Dysarthria and anarthria
1 1 1 1.0E-01 1 9.9E-03
SPASTIC PARAPLEGIA 16, X-LINKED (disorder)
1 0 1 1.0E-01 0 0
Malformation of the hepatic ductal plate
1 0 1 1.0E-01 0 0
CUI: C1865864
Disease: AMYOTROPHIC LATERAL SCLEROSIS 5
AMYOTROPHIC LATERAL SCLEROSIS 5
1 0 1 1.0E-01 0 0
CUI: C2931276
Disease: Spastic paraplegia 17
Spastic paraplegia 17
12 0 2 1.0E-01 0 0
CUI: C2931821
Disease: Nakamura Osame syndrome
Nakamura Osame syndrome
1 0 1 1.0E-01 0 0