Cerebral white matter atrophy
Symptom Information:
Symptom ID: | HPO:0012762 | |
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Is a (Whole tree): |
HPO:
MedDRA: |
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Database Frequency: | 3 / 7739 | |
Resource: | HPO |
All diseases associated with this symptom:
Hypomyelination - congenital cataract | (Orphanet:85163) |
Leukoencephalopathy - thalamus and brainstem anomalies - high lactate | (Orphanet:314051) |
Pyruvate dehydrogenase E3-binding protein deficiency | (Orphanet:255182) |