Focal T2 hyperintense basal ganglia lesion
Symptom Information:
Symptom ID: | HPO:0007183 | ||
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HPO:
MedDRA: |
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Database Frequency: | 6 / 7739 | ||
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All diseases associated with this symptom:
17q11.2 microduplication syndrome | (Orphanet:139474) |
Alpers syndrome | (Orphanet:726) |
Combined oxidative phosphorylation defect type 15 | (Orphanet:319524) |
Combined oxidative phosphorylation deficiency type 23 | (ORPHA:444013) |
Ethylmalonic encephalopathy | (Orphanet:51188) |
Pyruvate dehydrogenase E3-binding protein deficiency | (Orphanet:255182) |