M35.7
BillableHypermobility syndrome
Hypermobility syndrome
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Familial ligamentous laxity
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
- •reactive perforating collagenosisL87.1
- •ligamentous laxity, NOSM24.2
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
- •Ehlers-Danlos syndromesQ79.6
Related Codes(9)
M35.0Sjogren syndrome
M35.1Other overlap syndromes
M35.2Behcet's disease
M35.3Polymyalgia rheumatica
M35.4Diffuse (eosinophilic) fasciitis
M35.5Multifocal fibrosclerosis
M35.6Relapsing panniculitis [Weber-Christian]
M35.8Other specified systemic involvement of connective tissue
M35.9Systemic involvement of connective tissue, unspecified
ICD-11 Equivalents(1)
ICD-11 Equivalents
View full mappingCorresponding ICD-11 codes from the WHO crosswalk mapping
Also Known As / Clinical Terms(67)
SNOMED CT
- Marfan syndrome19346006
- Marfan's disease19346006
- Marfan's syndrome19346006
- Laxity of ligament27911000
- Musculoskeletal hypermobility40507009
- Marfanoid joint hypermobility syndrome57201002
- Local disease74217003
- Localised disease74217003
- Localized disease74217003
- Familial ligamentous laxity85551004
- Hypermobility syndrome85551004
- Musculoskeletal alteration129890008
- Scoliosis in skeletal dysplasia203661003
- Generalised benign joint hypermobility240261009
- Generalized benign joint hypermobility240261009
- Localised benign joint hypermobility240262002
- Localized benign joint hypermobility240262002
- Foot joint hypermobility298199008
- Metatarsophalangeal joint hypermobility298201005
- Spondyloepiphyseal dysplasia with joint laxity389160009
- SEMDJL1 - spondyloepimetaphyseal dysplasia with joint laxity type 11286833006
- Spondyloepimetaphyseal dysplasia with joint laxity Beighton type1286833006
- Spondyloepimetaphyseal dysplasia with joint laxity type 11286833006
- SEMDJL3 - spondyloepimetaphyseal dysplasia with joint laxity type 31286834000
- Spondyloepimetaphyseal dysplasia with joint laxity exocyst complex component 6B type1286834000
- Spondyloepimetaphyseal dysplasia with joint laxity type 31286834000
- Spondyloepimetaphyseal dysplasia with joint laxity, EXOC6B type1286834000
UMLS
- Familial ligamentous laxityC0152093
- Hypermobility SyndromeC0152093
- Hypermobility syndromeC0152093
- Hypermobility syndrome (disorder)C0152093
- Joint hypermobility syndromeC0152093
- benign hypermobility jointC0152093
- benign joint hypermobilityC0152093
- hypermobility syndromeC0152093
- hypermobility syndromesC0152093
Clinical Terms
- Musculoskeletal hypermobility
- Spondyloepiphyseal dysplasia with joint laxity
- Marfanoid joint hypermobility syndrome
- Familial ligamentous laxity
- Localised benign joint hypermobility
- Joint hypermobility syndrome
- Spondyloepimetaphyseal dysplasia with joint laxity type 3
- Generalized benign joint hypermobility
- Hypermobility syndrome (disorder)
- Localized disease
- Spondyloepimetaphyseal dysplasia with joint laxity exocyst complex component 6B type
- benign joint hypermobility
- Foot joint hypermobility
- Marfan's disease
- Spondyloepimetaphyseal dysplasia with joint laxity type 1
- Localized benign joint hypermobility
- Spondyloepimetaphyseal dysplasia with joint laxity Beighton type
- Musculoskeletal alteration
- Local disease
- Marfan syndrome
- Metatarsophalangeal joint hypermobility
- benign hypermobility joint
- Localised disease
- SEMDJL1 - spondyloepimetaphyseal dysplasia with joint laxity type 1
- SEMDJL3 - spondyloepimetaphyseal dysplasia with joint laxity type 3
- Spondyloepimetaphyseal dysplasia with joint laxity, EXOC6B type
- Marfan's syndrome
- Scoliosis in skeletal dysplasia
- Laxity of ligament
- Generalised benign joint hypermobility
- hypermobility syndromes
Frequently Asked Questions
What is the ICD-10 code for hypermobility syndrome?
The ICD-10-CM code for hypermobility syndrome is M35.7. The full clinical description is "Hypermobility syndrome". M35.7 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code M35.7 mean?
ICD-10-CM code M35.7 represents “Hypermobility 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 M35.7 a billable code?
Yes, M35.7 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is M35.7 in?
M35.7 is in Chapter 13: Diseases of the Musculoskeletal System and Connective Tissue (codes M00-M99).
What codes cannot be used with M35.7?
M35.7 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; reactive perforating collagenosis (L87.1); ligamentous laxity, NOS (M24.2-).
What SNOMED CT codes does M35.7 map to?
M35.7 maps to 15 SNOMED CT concepts: 85551004, 298199008, 240261009, 27911000, 74217003, and 10 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for M35.7?
M35.7 is linked to 1 UMLS Concept Unique Identifier: C0152093. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
How does M35.7 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like hypermobility 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 M35.7?
M35.7 maps to the ICD-11 code: LD28.1Y (Other specified types of Ehlers-Danlos syndrome).
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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.