ICD-10-CM Code M11.19
Familial chondrocalcinosis, multiple sites
Billable Code
Billable codes are sufficient justification for admission to an acute care hospital when used a principal diagnosis.M11.19 is a billable ICD code used to specify a diagnosis of familial chondrocalcinosis, multiple sites. A 'billable code' is detailed enough to be used to specify a medical diagnosis.
The ICD code M111 is used to code Chondrocalcinosis
Calcium pyrophosphate dihydrate (CPPD) crystal deposition disease, also known as chondrocalcinosis, pseudogout and pyrophosphate arthropathy is a rheumatologic disorder with varied symptoms and signs arising from the accumulation of crystals of calcium pyrophosphate dihydrate in the connective tissues. The alternative names emphasize particular aspects of the clinical or radiographic findings. The knee joint is the most commonly affected.
Specialty: | Rheumatology |
MeSH Codes: | D002805, D002805, D002805 |
ICD 9 Codes: | 712.3, 275.49, 712.3 |
Micrograph showing crystal deposition in an intervertebral disc. H&E stain.
MS-DRG Mapping
- DRG Group #553-554 - Bone diseases and arthropathies with MCC.
- DRG Group #553-554 - Bone diseases and arthropathies without MCC.
Related Concepts SNOMET-CT
- Familial chondrocalcinosis (disorder)
ICD-10-CM Alphabetical Index References for 'M11.19 - Familial chondrocalcinosis, multiple sites'
The ICD-10-CM Alphabetical Index links the below-listed medical terms to the ICD code M11.19. Click on any term below to browse the alphabetical index.
Equivalent ICD-9 Code GENERAL EQUIVALENCE MAPPINGS (GEM)
This is the official approximate match mapping between ICD9 and ICD10, as provided by the General Equivalency mapping crosswalk. This means that while there is no exact mapping between this ICD10 code M11.19 and a single ICD9 code, 712.39 is an approximate match for comparison and conversion purposes.
Parent Code: M11.1 - Familial chondrocalcinosis