Cerebral atrophy, progressive
Symptom Information:
| Symptom ID: | OMIM : No Id available | |
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HPO:
MedDRA: |
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| Database Frequency: | 4 / 7739 | |
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All diseases associated with this symptom:
| 3-methylglutaconic aciduria type 1 | (Orphanet:67046) |
| AICARDI-GOUTIERES SYNDROME 1 | (OMIM:225750) |
| CLN1 disease | (Orphanet:228329) |
| Progressive epilepsy-intellectual deficit, Finnish type | (Orphanet:1947) |