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)
- autoimmune disease, single organ or single cell-type -code to relevant condition category
- •circumscribed sclerodermaL94.0
- •neonatal sclerodermaP83.88
Excludes 2
Conditions not included here, but the patient may have both
- •arthropathic psoriasisL40.5
- •certain conditions originating in the perinatal periodP04-P96
- •certain infectious and parasitic diseasesA00-B99
- •compartment syndrome (traumatic)A-)T79
- •complications of pregnancy, childbirth and the puerperiumO9A)O00
- •congenital malformations, deformations, and chromosomal abnormalitiesQ00-Q99
- •endocrine, nutritional and metabolic diseasesE00-E88
- •injury, poisoning and certain other consequences of external causesS00-T88
- •neoplasmsC00-D49
- •symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classifiedR00-R94
Related Codes(4)
ICD-11 Equivalents(1)
ICD-11 Equivalents
View full mappingCorresponding ICD-11 codes from the WHO crosswalk mapping
Also Known As / Clinical Terms(94)
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
Clinical Terms
- CREST syndrome
- CRST - Calcinosis, Raynaud's phenomenon, sclerodactyly, telangiectasia syndrome
- CREST - Calcinosis, Raynaud's phenomenon, esophageal dysfunction, sclerodactyly, telangiectasia
- Raynaud phenomenon
- Calcinosis cutis, Raynaud's, esophageal dysfunction, sclerodactyly AND telangiectasia
- CREST - Calcinosis, Raynaud's phenomenon, sclerodactyly, oesophageal involvement, telangiectasia syndrome
- CRST syndrome
- Combination of calcinosis, Raynaud's phenomenon, esophageal dysfunction, sclerodactyly, telangiectasia
- Calcinosis cutis, Raynaud's, oesophageal dysfunction, sclerodactyly AND telangiectasia
- Calcinosis, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia syndrome (disorder)
- Systemic sclerosis with limited cutaneous involvement
- Calcinosis, Raynaud phenomenon, oesophageal dysmotility, sclerodactyly, and telangiectasia (CREST) syndrome
- Calcinosis, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia syndrome
- Limited cutaneous systemic sclerosis
- Secondary Raynaud phenomenon
- CREST Syndromes
- Limited systemic sclerosis
- Limited Cutaneous Systemic Scleroderma
- Calcinosis, Raynaud's phenomenon, Esophageal dismobility, Sclerodactyly, Telangiectasia Syndrome
- Raynaud's phenomenon
- Paroxysmal digital cyanosis
- CREST - Calcinosis, Raynaud's phenomenon, oesophageal dysfunction, sclerodactyly, telangiectasia
- Calcinosis cutis, Raynaud's, sclerodactyly AND telangiectasia
- Calcinosis, Raynaud's phenomenon, oesophageal dysmotility, sclerodactyly, and telangiectasia syndrome
- Secondary Raynaud's phenomenon
- Systemic sclerosis, limited
- crest
- Acrosclerosis
- CREST - Calcinosis, Raynaud's phenomenon, sclerodactyly, esophageal involvement, telangiectasia syndrome
- Calcinosis, Raynaud phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia (CREST) syndrome
- Calcinosis, Raynaud's phenomenon, oesophageal dysmotility, sclerodactyly, and telangiectasia (CREST) syndrome
- Calcinosis, Raynaud's phenomenon, sclerodactyly, and telangiectasia syndrome
- Calcinosis, Raynaud's phenomenon, sclerodactyly, and telangiectasia (CRST) syndrome
- Limited scleroderma
- Calcinosis, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia (CREST) syndrome
- Calcinosis, Raynaud's phenomenon, sclerodactyly, telangiectasia syndrome
- Syndrome, CREST
- Calcinosis, Raynaud phenomenon, sclerodactyly, and telangiectasia (CRST) syndrome
Frequently Asked Questions
What is the ICD-10 code for cr(e)st syndrome?
The ICD-10-CM code for cr(e)st syndrome is M34.1. The full clinical description is "CR(E)ST syndrome". M34.1 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code M34.1 mean?
ICD-10-CM code M34.1 represents “CR(E)ST syndrome”. It is classified under Chapter 13: Diseases of the Musculoskeletal System and Connective Tissue and 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.
How does M34.1 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like cr(e)st syndrome affect a person's functioning — body functions, activities, participation, and environmental factors. AutoICD provides ICF Core Sets for 12+ conditions and can map clinical text to ICF categories automatically. Browse the ICF directory to explore functioning codes.
What is the ICD-11 equivalent of M34.1?
M34.1 maps to the ICD-11 code: 4A42.2 (Limited systemic sclerosis).
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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.