M34.1
BillableCR(E)ST syndrome
CR(E)ST syndrome
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Combination of calcinosis, Raynaud's phenomenon, esophageal dysfunction, sclerodactyly, telangiectasia
Includes
Conditions included under this code
- autoimmune disease NOS
- collagen (vascular) disease NOS
- systemic autoimmune disease
- systemic collagen (vascular) disease
Excludes 1
Codes that cannot be used together with this code (mutual exclusion)
Excludes 2
Conditions not included here, but the patient may have both
- arthropathic psoriasis (L40.5-)
- certain conditions originating in the perinatal period (P04-P96)
- certain infectious and parasitic diseases (A00-B99)
- compartment syndrome (traumatic) (T79.A-)
- complications of pregnancy, childbirth and the puerperium (O00-O9A)
- congenital malformations, deformations, and chromosomal abnormalities (Q00-Q99)
- endocrine, nutritional and metabolic diseases (E00-E88)
- injury, poisoning and certain other consequences of external causes (S00-T88)
- neoplasms (C00-D49)
- symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified (R00-R94)
Also Known As / Clinical Terms
SNOMED CT
- CREST - Calcinosis, Raynaud's phenomenon, esophageal dysfunction, sclerodactyly, telangiectasia31848007
- CREST - Calcinosis, Raynaud's phenomenon, oesophageal dysfunction, sclerodactyly, telangiectasia31848007
- CREST - Calcinosis, Raynaud's phenomenon, sclerodactyly, esophageal involvement, telangiectasia syndrome31848007
- CREST - Calcinosis, Raynaud's phenomenon, sclerodactyly, oesophageal involvement, telangiectasia syndrome31848007
- CREST syndrome31848007
- Calcinosis cutis, Raynaud's, esophageal dysfunction, sclerodactyly AND telangiectasia31848007
- Calcinosis cutis, Raynaud's, oesophageal dysfunction, sclerodactyly AND telangiectasia31848007
- Calcinosis, Raynaud phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia (CREST) syndrome31848007
- Calcinosis, Raynaud phenomenon, oesophageal dysmotility, sclerodactyly, and telangiectasia (CREST) syndrome31848007
- Calcinosis, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia (CREST) syndrome31848007
- Calcinosis, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia syndrome31848007
- Calcinosis, Raynaud's phenomenon, oesophageal dysmotility, sclerodactyly, and telangiectasia (CREST) syndrome31848007
- Calcinosis, Raynaud's phenomenon, oesophageal dysmotility, sclerodactyly, and telangiectasia syndrome31848007
- CRST - Calcinosis, Raynaud's phenomenon, sclerodactyly, telangiectasia syndrome62382002
- CRST syndrome62382002
- Calcinosis cutis, Raynaud's, sclerodactyly AND telangiectasia62382002
- Calcinosis, Raynaud phenomenon, sclerodactyly, and telangiectasia (CRST) syndrome62382002
- Calcinosis, Raynaud's phenomenon, sclerodactyly, and telangiectasia (CRST) syndrome62382002
- Calcinosis, Raynaud's phenomenon, sclerodactyly, and telangiectasia syndrome62382002
- Calcinosis, Raynaud's phenomenon, sclerodactyly, telangiectasia syndrome62382002
- Paroxysmal digital cyanosis266261006
- Raynaud phenomenon266261006
- Raynaud's phenomenon266261006
- Acrosclerosis298285004
- Limited cutaneous systemic sclerosis298285004
- Systemic sclerosis with limited cutaneous involvement298285004
- Limited scleroderma299276009
- Limited systemic sclerosis299276009
- Systemic sclerosis, limited299276009
- Secondary Raynaud phenomenon356198000
- Secondary Raynaud's phenomenon356198000
UMLS
- CR(E)ST syndromeC0206138
- CREST - Calcinosis, Raynaud's phenomenon, esophageal dysfunction, sclerodactyly, telangiectasiaC0206138
- CREST - Calcinosis, Raynaud's phenomenon, oesophageal dysfunction, sclerodactyly, telangiectasiaC0206138
- CREST - Calcinosis, Raynaud's phenomenon, sclerodactyly, esophageal involvement, telangiectasia syndromeC0206138
- CREST - Calcinosis, Raynaud's phenomenon, sclerodactyly, oesophageal involvement, telangiectasia syndromeC0206138
- CREST SYNDROMEC0206138
- CREST SyndromeC0206138
- CREST SyndromesC0206138
- CREST syndromeC0206138
- Calcinosis cutis, Raynaud's, esophageal dysfunction, sclerodactyly AND telangiectasiaC0206138
- Calcinosis cutis, Raynaud's, oesophageal dysfunction, sclerodactyly AND telangiectasiaC0206138
- Calcinosis, Raynaud phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia (CREST) syndromeC0206138
- Calcinosis, Raynaud phenomenon, oesophageal dysmotility, sclerodactyly, and telangiectasia (CREST) syndromeC0206138
- Calcinosis, Raynaud's phenomenon, Esophageal dismobility, Sclerodactyly, Telangiectasia SyndromeC0206138
- Calcinosis, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia (CREST) syndromeC0206138
- Calcinosis, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia syndromeC0206138
- Calcinosis, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia syndrome (disorder)C0206138
- Calcinosis, Raynaud's phenomenon, oesophageal dysmotility, sclerodactyly, and telangiectasia (CREST) syndromeC0206138
- Calcinosis, Raynaud's phenomenon, oesophageal dysmotility, sclerodactyly, and telangiectasia syndromeC0206138
- Limited Cutaneous Systemic SclerodermaC0206138
- Syndrome, CRESTC0206138
- crestC0206138
- crest syndromeC0206138
- crst syndromeC0206138
- Combination of calcinosis, Raynaud's phenomenon, esophageal dysfunction, sclerodactyly, telangiectasiaC2895195
Frequently Asked Questions
What is ICD-10 code M34.1?
ICD-10-CM code M34.1 represents "CR(E)ST syndrome". It is a billable/specific code that can be used on a claim.
Is M34.1 a billable code?
Yes, M34.1 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is M34.1 in?
M34.1 is in Chapter 13: Diseases of the Musculoskeletal System and Connective Tissue (codes M00-M99).
What codes cannot be used with M34.1?
M34.1 has Excludes1 notes indicating codes that cannot be used together with it, including: autoimmune disease, single organ or single cell-type -code to relevant condition category; circumscribed scleroderma (L94.0); neonatal scleroderma (P83.88).
What SNOMED CT codes does M34.1 map to?
M34.1 maps to 6 SNOMED CT concepts: 298285004, 31848007, 62382002, 299276009, 266261006, and 1 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for M34.1?
M34.1 is linked to 2 UMLS Concept Unique Identifiers: C0206138, C2895195. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
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Includes SNOMED Clinical Terms® (SNOMED CT®) used by permission of SNOMED International. Includes content from the UMLS Metathesaurus, courtesy of the U.S. National Library of Medicine.