Myotonic dystrophy
ICD-10 Code
G71.11
Myotonic dystrophy
Definition
An inherited progressive disorder affecting the muscles. It is characterized by muscle wasting and hypotonia, cataracts, heart conduction defects and endocrinopathies.
Also known as inherited myotonic dystrophy — per MONDO
Also identified as
- DOID 450 per MONDO
- ICD10CM G71.11 per MONDO
- ICD9 359.2 per MONDO
- MESH D009223 per MONDO
- NCIT C84914 per MONDO
- Orphanet 206647 per MONDO
- SCTID 240104008 per MONDO
- UMLS C0027126 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 |