Abnormality of the basal ganglia
Symptom Information:
Symptom ID: | HPO:0002134 | ||||||||
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HPO:
MedDRA: |
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Database Frequency: | 13 / 7739 | ||||||||
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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) |