Increased neuronal autofluorescent lipopigment
Symptom Information:
Symptom ID: | HPO:0002074 | ||
Synonyms: |
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Quality: | |||
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Is a (Direct Parents): |
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Is a (Whole tree): |
HPO:
MedDRA: |
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Database Frequency: | 10 / 7739 | ||
Resource: |
All diseases associated with this symptom:
CLN1 disease | (Orphanet:228329) |
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) |
Late infantile neuronal ceroid lipofuscinosis | (Orphanet:168491) |
Progressive epilepsy-intellectual deficit, Finnish type | (Orphanet:1947) |