Hypomimia
Symptom Information:
Symptom ID: | OMIM : No Id available | |
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HPO:
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Database Frequency: | 3 / 7739 | |
Resource: |
All diseases associated with this symptom:
Autosomal recessive spastic paraplegia type 49 | (Orphanet:320385) |
Neuroferritinopathy | (Orphanet:157846) |
PARKINSON DISEASE 15, AUTOSOMAL RECESSIVE EARLY-ONSET | (OMIM:260300) |