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ICD-10-CM Codes Browse (Tabular) Diagnostic External Drug Neoplasm

Q77.3 – Chondrodysplasia punctata

Overview

Coding Notes

Active
Billable, valid for HIPAA-covered transactions

Type 1 Excludes

Rhizomelic chondrodysplasia punctata (E71.43)

GEM Conversion to ICD-9 CM

Fs: 10000 – Other osteodystrophies

MDC / MS-DRG Reference

OTHER MUSCULOSKELETAL SYSTEM AND CONNECTIVE TISSUE DIAGNOSES WITH MCC
OTHER MUSCULOSKELETAL SYSTEM AND CONNECTIVE TISSUE DIAGNOSES WITH CC
OTHER MUSCULOSKELETAL SYSTEM AND CONNECTIVE TISSUE DIAGNOSES WITHOUT CC/MCC

Back Reference of Diagnostic Codes


Sibling Codes

Achondrogenesis
Thanatophoric short stature
Short rib syndrome
Achondroplasia
Diastrophic dysplasia
Chondroectodermal dysplasia
Spondyloepiphyseal dysplasia
Other osteochondrodysplasia with defects of growth of tubular bones and spine
Osteochondrodysplasia with defects of growth of tubular bones and spine, unspecified

Parent Sibling Codes

Syndactyly
Reduction defects of upper limb
Reduction defects of lower limb
Reduction defects of unspecified limb
Other congenital malformations of limb(s)
Other congenital malformations of skull and face bones
Congenital malformations of spine and bony thorax
Osteochondrodysplasia with defects of growth of tubular bones and spine
Other osteochondrodysplasias
Congenital malformations of musculoskeletal system, not elsewhere classified

View in Tabular

Code Title
Q00-Q99 Congenital malformations, deformations and chromosomal abnormalities (Q00-Q99)
Q65-Q79 Congenital malformations and deformations of the musculoskeletal system (Q65-Q79)
Q77 Osteochondrodysplasia with defects of growth of tubular bones and spine
Q77.3 Chondrodysplasia punctata
Type 1 Excludes
Rhizomelic chondrodysplasia punctata (E71.43)