Facioscapulohumeral muscular dystrophy
ICD-10 Code
G71.02
Facioscapulohumeral muscular dystrophy
Definition
An autosomal dominant disorder affecting the skeletal muscles of the face, scapula, and upper arm. Patients present with muscle weakness in these anatomic areas. The muscle weakness eventually spreads to other skeletal muscles as well.
Also known as facioscapulohumeral dystrophy, facioscapulohumeral muscular dystrophy, facioscapulohumeral myopathy, FSH dystrophy, FSHD — per MONDO
Also identified as
- DOID 11727 per MONDO
- ICD10CM G71.02 per MONDO
- MESH D020391 per MONDO
- NCIT C84704 per MONDO
- Orphanet 269 per MONDO
- SCTID 399091004 per MONDO
- UMLS C0238288 per MONDO
Affected Organs
| Organ | Involvement | Source |
|---|---|---|
| Musculature | Disease Has Associated Anatomic Site | NCIT · CC BY 4.0 |
| Musculature | Disease Has Primary Anatomic Site | NCIT · CC BY 4.0 |
| Musculoskeletal system | Disease Has Associated Anatomic Site | NCIT · CC BY 4.0 |
| Musculoskeletal system | Disease Has Primary Anatomic Site | NCIT · CC BY 4.0 |
| Nervous system | Disease Has Associated Anatomic Site | NCIT · CC BY 4.0 |
| Nervous system | Disease Has Primary Anatomic Site | NCIT · CC BY 4.0 |
| Peripheral nervous system | Disease Has Associated Anatomic Site | NCIT · CC BY 4.0 |
| Peripheral nervous system | Disease Has Primary Anatomic Site | NCIT · CC BY 4.0 |