Autofluorescent lipopigment in neurons
Symptom Information:
Symptom ID: | OMIM : No Id available | |
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HPO:
MedDRA: |
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Database Frequency: | 11 / 7739 | |
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All diseases associated with this symptom:
CLN1 disease | (Orphanet:228329) |
CLN10 disease | (Orphanet:228337) |
CLN2 disease | (Orphanet:228349) |
CLN3 disease | (Orphanet:228346) |
CLN4A disease | (Orphanet:228340) |
CLN4B disease | (Orphanet:228343) |
CLN5 disease | (Orphanet:228360) |
CLN6 disease | (Orphanet:228363) |
CLN8 disease | (Orphanet:228354) |
Congenital neuronal ceroid lipofuscinosis | (Orphanet:168486) |
Progressive epilepsy-intellectual deficit, Finnish type | (Orphanet:1947) |