Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Paraplegia spastica tropica |
Is a |
False |
Spastic paraplegia |
Inferred relationship |
Some |
|
Hereditary spastic paraplegia |
Is a |
True |
Spastic paraplegia |
Inferred relationship |
Some |
|
Athetosis with spastic paraplegia |
Is a |
True |
Spastic paraplegia |
Inferred relationship |
Some |
|
A rare, syndromic intellectual disability characterized by macrocephaly, short stature, intellectual disability, variable degree of spastic paraplegia, central nervous system malformations (hydrocephalus, Dandy-Walker malformation), and dysmorphic features, such as high and broad forehead, midface hypoplasia, and small and broad hands and feet. There have been no further descriptions in the literature since 1993. |
Is a |
True |
Spastic paraplegia |
Inferred relationship |
Some |
|
A rare X-linked syndromic intellectual disability characterized by intellectual impairment of variable severity, progressive lower limb spasticity, and diffuse palmoplantar hyperkeratosis. Additional manifestations include pes cavus, extensor plantar responses, hand tremor, and mild dysmorphic facial features. |
Is a |
True |
Spastic paraplegia |
Inferred relationship |
Some |
|
Paraplegia, brachydactyly, cone-shaped epiphysis syndrome |
Is a |
False |
Spastic paraplegia |
Inferred relationship |
Some |
|
Intellectual disability-spasticity-ectrodactyly syndrome is a rare intellectual disability syndrome characterized by severe intellectual disability, spastic paraplegia (with wasting of the lower limbs) and distal transverse defects of the limbs (e.g. ectrodactyly, syndactyly, clinodactyly of the hands and/or feet). |
Is a |
False |
Spastic paraplegia |
Inferred relationship |
Some |
|