Abnormality of the basal ganglia

Symptom Information:

Symptom ID: HPO:0002134
Synonyms:
Basal ganglia disease [HPO:0002134]
Quality:
Cross references:
Is a (Direct Parents):
HPO         Abnormal basal ganglia MRI signal intensity
HPO         Small basal ganglia
HPO         Abnormality of the substantia nigra
HPO         Abnormality of the cerebral subcortex
Is a (Whole tree): HPO:
MedDRA:
Database Frequency: 13 / 7739
Resource:

All diseases associated with this symptom:

Childhood apraxia of speech (Orphanet:209908)
Combined oxidative phosphorylation defect type 17 (Orphanet:369913)
Combined oxidative phosphorylation defect type 4 (Orphanet:254925)
Intellectual deficit, X-linked - Dandy-Walker malformation - basal ganglia disease - Seizures (Orphanet:1568)
Leber plus disease (Orphanet:99718)
Leigh syndrome with nephrotic syndrome (Orphanet:255249)
Maternally-inherited Leigh syndrome (Orphanet:255210)
Mitochondrial DNA depletion syndrome, encephalomyopathic form with methylmalonic aciduria (Orphanet:1933)
Mitochondrial DNA depletion syndrome, myopathic form (Orphanet:254875)
Pontocerebellar hypoplasia, type 9 (OMIM:615809)
Pyruvate dehydrogenase E1-alpha deficiency (Orphanet:79243)
Severe X-linked mitochondrial encephalomyopathy (Orphanet:238329)
Thiamine-responsive encephalopathy (Orphanet:199348)