Morphological abnormality of the pyramidal tract

Symptom Information:

Symptom ID: HPO:0002062
Synonyms:
Pyramidal tract disease [HPO:0002062]
Quality:
Cross references:
Is a (Direct Parents):
Is a (Whole tree): HPO:
MedDRA:
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)