Fingerprint intracellular accumulation of autofluorescent lipopigment storage material
Symptom Information:
Symptom ID: | HPO:0003208 | ||||
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Is a (Direct Parents): |
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Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of metabolism/homeostasis(HPO:0001939) Abnormality of cell physiology(HPO:0011017) Intracellular accumulation of autofluorescent lipopigment storage material(HPO:0003204) Fingerprint intracellular accumulation of autofluorescent lipopigment storage material(HPO:0003208) MedDRA: |
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Database Frequency: | 8 / 7739 | ||||
Resource: |
All diseases associated with this symptom:
CLN11 disease | (Orphanet:314629) |
CLN3 disease | (Orphanet:228346) |
CLN4A disease | (Orphanet:228340) |
CLN4B disease | (Orphanet:228343) |
CLN5 disease | (Orphanet:228360) |
CLN6 disease | (Orphanet:228363) |
CLN9 disease | (Orphanet:228357) |
Progressive myoclonic epilepsy type 3 | (Orphanet:263516) |