Progressive spasticity
Symptom Information:
Symptom ID: | HPO:0002191 | |||
Synonyms: |
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Quality: | ||||
Cross references: |
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Is a (Direct Parents): |
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Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of the nervous system(HPO:0000707) Abnormality of nervous system physiology(HPO:0012638) Abnormality of central motor function(HPO:0011442) Abnormal pyramidal signs(HPO:0007256) Hypertonia(HPO:0001276) Spasticity(HPO:0001257) Progressive spasticity(HPO:0002191) MedDRA: |
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Database Frequency: | 12 / 7739 | |||
Resource: |
All diseases associated with this symptom:
Autosomal dominant spastic paraplegia type 13 | (Orphanet:100994) |
Autosomal dominant spastic paraplegia type 4 | (Orphanet:100985) |
Autosomal dominant spastic paraplegia type 6 | (Orphanet:100988) |
Autosomal recessive spastic paraplegia type 14 | (Orphanet:100995) |
Behr syndrome | (Orphanet:1239) |
GTP cyclohydrolase I deficiency | (Orphanet:2102) |
KRABBE DISEASE | (OMIM:245200) |
Krabbe disease | (Orphanet:487) |
LUBS X-LINKED MENTAL RETARDATION SYNDROME | (OMIM:300260) |
Pelizaeus-Merzbacher-like due to GJC2 mutation | (Orphanet:280282) |
Pelizaeus-Merzbacher-like due to HSPD1 mutation | (Orphanet:280288) |
Pontocerebellar hypoplasia, type 9 | (OMIM:615809) |