Morphological abnormality of the pyramidal tract
Symptom Information:
Symptom ID: | HPO:0002062 | |
Synonyms: |
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Quality: | ||
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Is a (Whole tree): |
HPO:
MedDRA: |
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Database Frequency: | 24 / 7739 | |
Resource: |
All diseases associated with this symptom:
AICARDI-GOUTIERES SYNDROME 1 | (OMIM:225750) |
AMYOTROPHIC LATERAL SCLEROSIS 8 | (OMIM:608627) |
Autosomal dominant spastic paraplegia type 4 | (Orphanet:100985) |
Autosomal dominant spastic paraplegia type 8 | (Orphanet:100989) |
CHARCOT-MARIE-TOOTH PERONEAL MUSCULAR ATROPHY AND FRIEDREICH ATAXIA,COMBINED | (OMIM:302900) |
Coats plus syndrome | (Orphanet:313838) |
Dihydropyrimidinuria | (Orphanet:38874) |
Dystonia 16 | (Orphanet:210571) |
Encephalopathy, axonal, with necrotizing myopathy, cardiomyopathy,and cataracts | (OMIM:225740) |
FRIEDREICH ATAXIA AND CONGENITAL GLAUCOMA | (OMIM:229310) |
Friedreich ataxia 2 | (OMIM:601992) |
Giant axonal neuropathy | (Orphanet:643) |
Huntington disease-like 3 | (Orphanet:157946) |
Hyperornithinemia-hyperammonemia-homocitrullinuria | (Orphanet:415) |
Infantile dystonia-parkinsonism | (Orphanet:238455) |
Infantile neuroaxonal dystrophy | (Orphanet:35069) |
L-2-hydroxyglutaric aciduria | (Orphanet:79314) |
Paroxysmal dystonic choreathetosis with episodic ataxia and spasticity | (Orphanet:53583) |
Progressive supranuclear palsy - parkinsonism | (Orphanet:240085) |
Spinocerebellar ataxia type 10 | (Orphanet:98761) |
Spinocerebellar ataxia type 13 | (Orphanet:98768) |
Spinocerebellar ataxia type 8 | (Orphanet:98760) |
Thiamine-responsive encephalopathy | (Orphanet:199348) |
X-linked spinocerebellar ataxia type 4 | (Orphanet:85292) |