Q78.8

Other specified osteochondrodysplasias

Billable / specificPOA exempt

Q78.8 is a billable, specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes in FY2027.

Inclusion terms

Applicable to

  • Osteopoikilosis

Includes (from Q78)

  • Note: Codes from this chapter are not for use on maternal records

Excludes2

Not included here — may be reported together when both conditions exist.

  • inborn errors of metabolism (E70-E88) (from Q78)
  • congenital myotonic chondrodystrophy (G71.13) (from Q78)

Also known as

  • Osteopoikilosis
  • Abnormal, abnormality, abnormalities, synchondrosis
  • Caffey's syndrome
  • Chondrodysplasia, metaphyseal
  • Deficiency, deficient, short stature homeobox gene, with dyschondrosteosis
  • Dysplasia, craniometaphyseal
  • Hypoplasia, hypoplastic, cartilage hair
  • Leri's pleonosteosis
  • Osteochondrodysplasia, specified NEC
  • Osteopathia condensans disseminata
  • Segmentation, incomplete, bone NEC
  • Stippled epiphyses
  • Synchondrosis, abnormal
  • Synostosis

Parent code

  • Q78Other osteochondrodysplasiasHeader

Related codes

  • Q78.0Osteogenesis imperfectaBillable
  • Q78.1Polyostotic fibrous dysplasiaBillable
  • Q78.2OsteopetrosisBillable
  • Q78.3Progressive diaphyseal dysplasiaBillable
  • Q78.4EnchondromatosisBillable
  • Q78.5Metaphyseal dysplasiaBillable
  • Q78.6Multiple congenital exostosesBillable
  • Q78.9Osteochondrodysplasia, unspecifiedBillable

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