Oth acquired deformities of ms sys and connective tissue (M95)

• ICD-10 Index

  • Diseases of the musculoskeletal system and connective tissue (M00–M99)

    • Other disorders of the musculoskeletal system and connective tissue (M95)

      • Oth acquired deformities of ms sys and connective tissue (M95)

        • M95 - Oth acquired deformities of ms sys and connective tissue NON-BILLABLE CODE
        • M95.0 - Acquired deformity of nose BILLABLE CODE
        • M95.1 - Cauliflower ear NON-BILLABLE CODE
        • M95.10 - Cauliflower ear, unspecified ear BILLABLE CODE
        • M95.11 - Cauliflower ear, right ear BILLABLE CODE
        • M95.12 - Cauliflower ear, left ear BILLABLE CODE
        • M95.2 - Other acquired deformity of head BILLABLE CODE
        • M95.3 - Acquired deformity of neck BILLABLE CODE
        • M95.4 - Acquired deformity of chest and rib BILLABLE CODE
        • M95.5 - Acquired deformity of pelvis BILLABLE CODE
        • M95.8 - Oth acquired deformities of musculoskeletal system BILLABLE CODE
        • M95.9 - Acquired deformity of musculoskeletal system, unspecified BILLABLE CODE

Clinical Information for Oth acquired deformities of ms sys and connective tissue (M95)

Craniosynostoses - Premature closure of one or more CRANIAL SUTURES. It often results in plagiocephaly. Craniosynostoses that involve multiple sutures are sometimes associated with congenital syndromes such as ACROCEPHALOSYNDACTYLIA; and CRANIOFACIAL DYSOSTOSIS.

Plagiocephaly - The condition characterized by uneven or irregular shape of the head often in parallelogram shape with a flat spot on the back or one side of the head. It can either result from the premature CRANIAL SUTURE closure (CRANIOSYNOSTOSIS) or from external forces (NONSYNOSTOTIC PLAGIOCEPHALY).

Plagiocephaly, Nonsynostotic - A deformity of the SKULL that is not due to bone fusion (SYNOSTOSIS), such as craniosynostoses, and is characterized by an asymmetric skull and face. It is observed with an increased frequency in INFANTS after the adoption of supine sleeping recommendations to prevent SUDDEN INFANT DEATH SYNDROME.

Pectus Carinatum - A developmental anomaly characterized by abnormal anterior protrusion of the STERNUM and adjacent COSTAL CARTILAGE.

Instructional Notations

Type 2 Excludes Type 2 Excludes
A type 2 excludes note represents "Not included here". An excludes2 note indicates that the condition excluded is not part of the condition represented by the code, but a patient may have both conditions at the same time. When an Excludes2 note appears under a code, it is acceptable to use both the code and the excluded code together, when appropriate.

• acquired absence of limbs and organs Z89 Z90
• acquired deformities of limbs M20 M21
• congenital malformations and deformations of the musculoskeletal system Q65 Q79
• deforming dorsopathies M40 M43
• dentofacial anomalies [including malocclusion] M26
• postprocedural musculoskeletal disorders M96