Concept information
...
Genetic disease
Hereditary disease
Autosomal hereditary disorder
Dominant hereditary disorder, NOS
Preferred term
Autosomal dominant hereditary spastic paraplegia
Type
-
http://www.irandoc.ac.ir/onto/irandoc-meta/Concept
Broader concept
Narrower concepts
- Autosomal dominant familial spastic paraplegia type 3
- Autosomal dominant spastic paraplegia type 10 (disorder)
- Autosomal dominant spastic paraplegia type 12 (disorder)
- Autosomal dominant spastic paraplegia type 13 (disorder)
- Autosomal dominant spastic paraplegia type 19
- Autosomal dominant spastic paraplegia type 29 (disorder)
- Autosomal dominant spastic paraplegia type 31 (disorder)
- Autosomal dominant spastic paraplegia type 36 (disorder)
- Autosomal dominant spastic paraplegia type 37 (disorder)
- Autosomal dominant spastic paraplegia type 38 (disorder)
- Autosomal dominant spastic paraplegia type 3 (disorder)
- Autosomal dominant spastic paraplegia type 41 (disorder)
- Autosomal dominant spastic paraplegia type 42
- Autosomal dominant spastic paraplegia type 4 (disorder)
- Autosomal dominant spastic paraplegia type 8
- Silver disease
- Spastic paraplegia, nephritis, deafness syndrome (disorder)
- Spastic paraplegia, neuropathy, poikiloderma syndrome (disorder)
- Spastic paraplegia with Paget disease of bone syndrome (disorder)
- Spastic paraplegia with precocious puberty syndrome (disorder)
Associated morphology
Clinical course
Finding site
In other languages
URI
http://www.irandoc.acir/onto/irandoc/737227004
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