Concept information
Preferred term
Autosomal recessive hereditary spastic paraplegia
Type
-
http://www.irandoc.ac.ir/onto/irandoc-meta/Concept
Narrower concepts
- Autosomal recessive complex spastic paraplegia due to Kennedy pathway dysfunction (disorder)
- Autosomal recessive spastic paraplegia type 27
- Autosomal recessive spastic paraplegia type 35
- Autosomal recessive spastic paraplegia type 45 (disorder)
- Autosomal recessive spastic paraplegia type 48 (disorder)
- Autosomal recessive spastic paraplegia type 56 (disorder)
- Autosomal recessive spastic paraplegia type 5A
- Autosomal recessive spastic paraplegia type 62
- Autosomal recessive spastic paraplegia type 75 (disorder)
- Autosomal recessive spastic paraplegia type 76 (disorder)
- Autosomal recessive spastic paraplegia type 77
- Autosomal recessive spastic paraplegia type 78 (disorder)
- Autosomal recessive spastic paraplegia type 9B
- Infantile-onset ascending hereditary spastic paralysis
- Kyphoscoliosis, lateral tongue atrophy, hereditary spastic paraplegia syndrome
- Postnatal microcephaly, infantile hypotonia, spastic diplegia, dysarthria, intellectual disability syndrome
- SPOAN and SPOAN-related disorder
- SPPRS (spastic paraplegia, psychomotor retardation, seizures) syndrome
Associated morphology
Clinical course
Finding site
Is a
- 39912006
- 85995004
In other languages
URI
http://www.irandoc.acir/onto/irandoc/1187279003
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