Focal T2 hyperintense basal ganglia lesion

Symptom Information:

Symptom ID: HPO:0007183
Synonyms:
Hyperintense lesions in the basal ganglia on MRI [OMIM:Hyperintense lesions in the basal ganglia on MRI]
Quality:
Cross references:
OMIM: "Hyperintense lesions in the basal ganglia on MRI" [OMIM:Hyperintense lesions in the basal ganglia on MRI]
Is a (Direct Parents):
HPO         Abnormality of the basal ganglia
Is a (Whole tree): HPO:
MedDRA:
Database Frequency: 6 / 7739
Resource:

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)