Cerebral inclusion bodies
Symptom Information:
Symptom ID: | HPO:0100314 | ||
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Is a (Whole tree): |
HPO:
MedDRA: |
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Database Frequency: | 2 / 7739 | ||
Resource: |
All diseases associated with this symptom:
Glycogen storage disease due to glycogen branching enzyme deficiency | (Orphanet:367) |
Neurodegeneration with brain iron accumulation due to C19orf12 mutation | (Orphanet:289560) |