Increased cerebral lipofuscin

Symptom Information:

Symptom ID: HPO:0011813
Synonyms:
Quality:
Cross references:
Is a (Direct Parents):
HPO         Atrophy/Degeneration affecting the central nervous system
Is a (Whole tree): HPO:
MedDRA:
Database Frequency: 4 / 7739
Resource:

All diseases associated with this symptom:

Atypical Gaucher disease due to saposin C deficiency (Orphanet:309252)
Glycogen storage disease due to LAMP-2 deficiency (Orphanet:34587)
Hermansky-Pudlak syndrome (Orphanet:79430)
Hermansky-Pudlak syndrome with pulmonary fibrosis (Orphanet:231500)