Macrophagic myofasciitis
General Information (adopted from Orphanet):
Synonyms, Signs: |
MMF |
Number of Symptoms | 7 |
OrphanetNr: | 592 |
OMIM Id: |
|
ICD-10: |
M60.8 |
UMLs: |
C2931639 |
MeSH: |
C537829 |
MedDRA: |
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Snomed: |
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Prevalence, inheritance and age of onset:
Prevalence: | No data available. |
Inheritance: |
|
Age of onset: |
Childhood Adolescent Adult Elderly [Orphanet] |
Disease classification (adopted from Orphanet):
Parent Diseases: |
Acquired skeletal muscle disease
-Rare neurologic disease |
Symptom Information:
|
(HPO:0005059) | Arthralgia/arthritis | Very frequent [Orphanet] | 141 / 7739 | |||
|
(HPO:0011227) | Elevated C-reactive protein level | Very frequent [Orphanet] | 55 / 7739 | |||
|
(HPO:0001945) | Fever | Very frequent [Orphanet] | 218 / 7739 | |||
|
(HPO:0003326) | Myalgia | Very frequent [Orphanet] | 143 / 7739 | |||
|
(HPO:0001324) | Muscle weakness | Very frequent [Orphanet] | 859 / 7739 | |||
|
(HPO:0003457) | EMG abnormality | Occasional [Orphanet] | 78 / 7739 | |||
|
(HPO:0030089) | Abnormal muscle fiber protein expression | Very frequent [Orphanet] | 64 / 7739 |
Associated genes:
ClinVar (via SNiPA)
Gene symbol | Variation | Clinical significance | Reference |
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