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)
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)
- Ehlers-Danlos syndromes (Q79.6-)
Also Known As / Clinical Terms
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
Frequently Asked Questions
What is ICD-10 code M35.7?
ICD-10-CM code M35.7 represents "Hypermobility syndrome". It 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.
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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.