Spastic paraparesis
Symptom Information:
Symptom ID: | HPO:0002313 | ||||
Synonyms: |
|
||||
Quality: | |||||
Cross references: |
|
||||
Is a (Direct Parents): |
|
||||
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) Weakness due to upper motor neuron dysfunction(HPO:0010549) Paraplegia/paraparesis(HPO:0010551) Paraparesis(HPO:0002385) Spastic paraparesis(HPO:0002313) Hypertonia(HPO:0001276) Spasticity(HPO:0001257) Lower limb spasticity(HPO:0002061) Spastic paraparesis(HPO:0002313) MedDRA: |
||||
Database Frequency: | 33 / 7739 | ||||
Resource: |
All diseases associated with this symptom:
3-methylglutaconic aciduria type 3 | (Orphanet:67047) |
Arachnoiditis | (Orphanet:137817) |
Autosomal dominant spastic paraplegia type 31 | (Orphanet:101011) |
Autosomal dominant spastic paraplegia type 4 | (Orphanet:100985) |
Autosomal recessive spastic ataxia - optic atrophy - dysarthria | (Orphanet:254343) |
Autosomal recessive spastic paraplegia type 20 | (Orphanet:101000) |
Autosomal recessive spastic paraplegia type 21 | (Orphanet:101001) |
Autosomal recessive spastic paraplegia type 35 | (Orphanet:171629) |
Autosomal recessive spastic paraplegia type 48 | (Orphanet:306511) |
Autosomal recessive spastic paraplegia type 7 | (Orphanet:99013) |
BRANCHIAL MYOCLONUS WITH SPASTIC PARAPARESIS AND CEREBELLAR ATAXIA | (OMIM:113610) |
Behr syndrome | (Orphanet:1239) |
Beta-propeller protein-associated neurodegeneration | (Orphanet:329284) |
Cirrhosis-dystonia-polycythemia-hypermanganesemia syndrome | (Orphanet:309854) |
Classical phenylketonuria | (Orphanet:79254) |
Early-onset spastic ataxia-neuropathy syndrome | (Orphanet:313772) |
Gaucher disease type 3 | (Orphanet:77261) |
Hyperornithinemia-hyperammonemia-homocitrullinuria | (Orphanet:415) |
Leber plus disease | (Orphanet:99718) |
MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 2 | (OMIM:615157) |
NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 6 | (OMIM:615643) |
Neurologic Waardenburg-Shah syndrome | (Orphanet:163746) |
Oculofaciocardiodental syndrome | (Orphanet:2712) |
Pelizaeus-Merzbacher-like disease | (Orphanet:280270) |
Pelizaeus-Merzbacher-like due to AIMP1 mutation | (Orphanet:280293) |
Pelizaeus-Merzbacher-like due to GJC2 mutation | (Orphanet:280282) |
Pyruvate dehydrogenase E3-binding protein deficiency | (Orphanet:255182) |
SPINOCEREBELLAR ATAXIA 40 | (OMIM:616053) |
Spastic paraparesis - deafness | (Orphanet:2815) |
Spastic paraplegia - epilepsy - intellectual deficit | (Orphanet:2816) |
Spastic paraplegia type 2 | (Orphanet:99015) |
Tropical spastic paraparesis | (Orphanet:289326) |
Waardenburg-Shah syndrome | (Orphanet:897) |