Diagnosis Code

Q78.5 METAPHYSEAL DYSPLASIA


Code Information

Diagnosis Code: Q78.5

Short Description: Metaphyseal dysplasia

Long Description: Metaphyseal dysplasia

The code Q78.5 is VALID for claim submission

Code Classification:

  • Congenital malformations, deformations and chromosomal abnormalities (Q00-Q99)
    • Congenital malformations and deformations of the musculoskeletal system (Q65-Q79)
      • Other osteochondrodysplasias (Q78)
        • Q78.5 Metaphyseal dysplasia

Code Version: 2022 ICD-10-CM


Synonyms

  • Acroscyphodysplasia
  • Autosomal recessive spondylometaphyseal dysplasia Megarbane type
  • Axial spondylometaphyseal dysplasia
  • Bowing of upper limb
  • Congenital bowing of long bone
  • Congenital deformity of bone of forearm
  • Congenital maxillary hypoplasia
  • Craniometaphyseal dysplasia
  • Craniometaphyseal dysplasia
  • Craniometaphyseal dysplasia - mild type
  • Craniometaphyseal dysplasia - severe type
  • Hypoplasia of maxillary bone
  • Intrauterine growth restriction, metaphyseal dysplasia, adrenal hypoplasia congenita, and genital anomaly syndrome
  • Kozlowski spondylometaphyseal dysplasia
  • Lentiglobus
  • Metaphyseal chondrodysplasia
  • Metaphyseal chondrodysplasia, Jansen type
  • Metaphyseal chondrodysplasia, McKusick type
  • Metaphyseal chondrodysplasia, Schmid type
  • Metaphyseal chondrodysplasia, Sedaghatian type
  • Metaphyseal chondrodysplasia, Spahr type
  • Metaphyseal dysplasia Braun Tinschert type
  • Metaphyseal dysplasia, maxillary hypoplasia, brachydactyly syndrome
  • Microphakia
  • Microspherophakia
  • Microspherophakia with metaphyseal dysplasia syndrome
  • Osteosclerosis
  • Osteosclerotic metaphyseal dysplasia
  • Overgrowth, metaphyseal undermodeling, spondylar dysplasia syndrome
  • Pyle metaphyseal dysplasia
  • Regressive spondylometaphyseal dysplasia
  • Spherophakia
  • Spondyloenchondrodysplasia
  • Spondylometaphyseal dysplasia
  • Spondylometaphyseal dysplasia - Sutcliffe type
  • Spondylometaphyseal dysplasia A4 type
  • Spondylometaphyseal dysplasia Czarny Ratajczak type
  • Spondylometaphyseal dysplasia, bowed forearms, facial dysmorphism syndrome
  • Ulna metaphyseal dysplasia syndrome

Diagnostic Related Group(s)

The code Q78.5 is grouped in the following Diagnostic Related Group(s) (MS-DRG v39.0)
  • Other Musculoskeletal System And Connective Tissue Diagnoses With Mcc (564)
  • Other Musculoskeletal System And Connective Tissue Diagnoses With Cc (565)
  • Other Musculoskeletal System And Connective Tissue Diagnoses Without Cc/mcc (566)

References to Index of Diseases and Injuries

The code Q78.5 has the following ICD-10-CM references to the Index of Diseases and Injuries
  • Inclusion Terms:
    • Pyle's syndrome

Crosswalk Information

ICD-10 Code ICD-9 Code ICD-9 Description
Q78.5 Right Arrow 756.59 Osteodystrophy NEC

This ICD-10 to ICD-9 data is based on the 2018 General Equivalency Mapping (GEM) files published by the Centers for Medicare & Medicaid Services (CMS) for informational purposes only. The data is not an ICD-10 conversion tool and doesn’t guarantee clinical accuracy.

Similar Codes

ICD-10 Code ICD-10 Description
Q78 Other osteochondrodysplasias
Q78.0 Osteogenesis imperfecta
Q78.1 Polyostotic fibrous dysplasia
Q78.2 Osteopetrosis
Q78.3 Progressive diaphyseal dysplasia
Q78.4 Enchondromatosis
Q78.6 Multiple congenital exostoses
Q78.8 Other specified osteochondrodysplasias
Q78.9 Osteochondrodysplasia, unspecified


This page was last updated on: 10/1/2023