Category · FY2027
Q77 Osteochondrodysplasia with defects of growth of tubular bones and spine
- Header · not billable
Q77 is not billable. The category heads 10 billable codes in FY2027: the 10 codes directly below it.
Index → code
Where it sits
- Chapter 17 Congenital malformations, deformations, chromosomal abnormalities, and genetic disorders (Q00-QA1)
- Q65-Q79 Congenital malformations and deformations of the musculoskeletal system (Q65-Q79)
- Q77 Osteochondrodysplasia with defects of growth of tubular bones and spine
- Billable codes
- 10
- Subdivisions
- 10
- CC / MCC codes
- 1 / 0
- HCC V28 codes
- 0
- New FY2027
- 0
- Index entries
- 33
Codes in Q77
- Q77.0AchondrogenesisBillableExempt
Inclusion terms 1
Inclusion terms
- Hypochondrogenesis
- Q77.1Thanatophoric short statureBillableExempt
- Q77.2Short rib syndromeBillableCCExempt
Inclusion terms 1
Inclusion terms
- Asphyxiating thoracic dysplasia [Jeune]
- Q77.3Chondrodysplasia punctataBillableExempt
Excludes1 1
Excludes1
- Rhizomelic chondrodysplasia punctata (E71.540) E71.540
- Q77.4AchondroplasiaBillableExempt
Inclusion terms 2
Inclusion terms
- Hypochondroplasia
- Osteosclerosis congenita
- Q77.5Diastrophic dysplasiaBillableExempt
- Q77.6Chondroectodermal dysplasiaBillableExempt
Inclusion terms 1
Inclusion terms
- Ellis-van Creveld syndrome
- Q77.7Spondyloepiphyseal dysplasiaBillableExempt
- Q77.8Other osteochondrodysplasia with defects of growth of tubular bones and spineBillableExempt
- Q77.9Osteochondrodysplasia with defects of growth of tubular bones and spine, unspecifiedBillableExempt
CC/MCC: as a secondary diagnosis, unless the principal diagnosis is on the code’s PDX exclusion list (MS-DRG v44 Appendix C; list on the code card).
Instructions
At Q77
Excludes2
- congenital myotonic chondrodystrophy (G71.13) G71.13
Notes that also apply
Chapter 17 instructions (Notes 1, Excludes2 1): printed on the chapter 17 page.
Index entries
- Achondrogenesis → Q77.0
- Hypochondrogenesis → Q77.0
- Thanatophoric dwarfism or short stature → Q77.1
- Jeune's disease → Q77.2
- Conradi (-Hunermann) disease → Q77.3
- Achondroplasia (osteosclerosis congenita) → Q77.4
- Chondrogenesis imperfecta → Q77.4
- Hypochondroplasia → Q77.4
- Chondroectodermal dysplasia → Q77.6
- Ellis-van Creveld syndrome (chondroectodermal dysplasia) → Q77.6
- Leri-Weill syndrome → Q77.8
- Dwarfism›thanatophoric → Q77.1
- Dysplasia›asphyxiating thoracic (congenital) → Q77.2
- Dystrophy, dystrophia›thoracic, asphyxiating → Q77.2
- Short, shortening, shortness›rib syndrome → Q77.2
- Chondrodysplasia›calcificans congenita → Q77.3
- Chondrodysplasia›punctata → Q77.3
- Chondrodystrophy, chondrodystrophia (familial) (fetalis) (hypoplastic)›calcificans congenita → Q77.3
- Chondrodystrophy, chondrodystrophia (familial) (fetalis) (hypoplastic)›punctata → Q77.3
- Chondrodysplasia›fetalis → Q77.4
- Dwarfism›achondroplastic → Q77.4
- Dwarfism›hypochondroplastic → Q77.4
- Osteosclerosis›congenita → Q77.4
- Dysplasia›dystrophic → Q77.5
- Disease, diseased›Ellis-van Creveld (chondroectodermal dysplasia) → Q77.6
- Dysplasia›chondroectodermal → Q77.6
- Syndrome›chondroectodermal dysplasia → Q77.6
- Syndrome›Ellis-van Creveld → Q77.6
- Dysplasia›spondyloepiphyseal → Q77.7
- Dwarfism›metatropic → Q77.8
- Osteochondrodysplasia›with defects of growth of tubular bones and spine → Q77.9
- Syndrome›short›rib → Q77.2
- Osteochondrodysplasia›with defects of growth of tubular bones and spine›specified NEC → Q77.8
NCHS Alphabetic Index. Index first, then the Tabular List.