Concept information
Preferred term
Complicated hereditary spastic paraplegia
Type
-
http://www.irandoc.ac.ir/onto/irandoc-meta/Concept
Broader concept
Narrower concepts
- Autosomal dominant spastic paraplegia type 29 (disorder)
- Autosomal dominant spastic paraplegia type 36 (disorder)
- Autosomal dominant spastic paraplegia type 38 (disorder)
- Autosomal recessive spastic paraplegia type 11 (disorder)
- Autosomal recessive spastic paraplegia type 14
- Autosomal recessive spastic paraplegia type 18 (disorder)
- Autosomal recessive spastic paraplegia type 21
- Autosomal recessive spastic paraplegia type 23 (disorder)
- Autosomal recessive spastic paraplegia type 25 (disorder)
- Autosomal recessive spastic paraplegia type 26 (disorder)
- Autosomal recessive spastic paraplegia type 32 (disorder)
- Autosomal recessive spastic paraplegia type 39 (disorder)
- Autosomal recessive spastic paraplegia type 43 (disorder)
- Autosomal recessive spastic paraplegia type 44 (disorder)
- Autosomal recessive spastic paraplegia type 46 (disorder)
- Autosomal recessive spastic paraplegia type 53 (disorder)
- Autosomal recessive spastic paraplegia type 54 (disorder)
- Autosomal recessive spastic paraplegia type 58
- Autosomal recessive spastic paraplegia type 59
- Autosomal recessive spastic paraplegia type 60
- Autosomal recessive spastic paraplegia type 61 (disorder)
- Autosomal recessive spastic paraplegia type 63 (disorder)
- Autosomal recessive spastic paraplegia type 64 (disorder)
- Autosomal recessive spastic paraplegia type 66
- Autosomal recessive spastic paraplegia type 67 (disorder)
- Autosomal recessive spastic paraplegia type 69
- Autosomal recessive spastic paraplegia type 70 (disorder)
- Hereditary sensory and autonomic neuropathy due to TECPR2 mutation
- Hereditary sensory and autonomic neuropathy with spastic paraplegia (disorder)
- Mitochondrially encoded ATP synthase membrane subunit 6-related mitochondrial spastic paraplegia
- Severe intellectual disability and progressive spastic paraplegia
- Silver disease
- Spastic paraplegia, facial cutaneous lesion syndrome (disorder)
- Spastic paraplegia, glaucoma, intellectual disability syndrome
- Spastic paraplegia, nephritis, deafness syndrome (disorder)
- Spastic paraplegia, neuropathy, poikiloderma syndrome (disorder)
- Spastic paraplegia, retinal degeneration syndrome
- Spastic paraplegia with Paget disease of bone syndrome (disorder)
- Spastic paraplegia with precocious puberty syndrome (disorder)
- SPOAN and SPOAN-related disorder
Associated morphology
Clinical course
Finding site
In other languages
-
Persian
URI
http://www.irandoc.acir/onto/irandoc/230261006
{{label}}
{{#each values }} {{! loop through ConceptPropertyValue objects }}
{{#if prefLabel }}
{{/if}}
{{/each}}
{{#if notation }}{{ notation }} {{/if}}{{ prefLabel }}
{{#ifDifferentLabelLang lang }} ({{ lang }}){{/ifDifferentLabelLang}}
{{#if vocabName }}
{{ vocabName }}
{{/if}}