ICD-10-CM Codes
Q00-Q99
Q65-Q79
Q77-
2023 ICD-10-CM Diagnosis Code Q77.3

2023 ICD-10-CM Diagnosis Code Q77.3

Chondrodysplasia punctata

2016

2017

2018

2019

2020

2021

2022

2023

Billable/Specific Code

POA Exempt

Q77.3 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.
The 2023 edition of ICD-10-CM Q77.3 became effective on October 1, 2022.
This is the American ICD-10-CM version of Q77.3 - other international versions of ICD-10 Q77.3 may differ.

Type 1 Excludes

Type 1 Excludes Help

A type 1 excludes note is a pure excludes. It means "not coded here". A type 1 excludes note indicates that the code excluded should never be used at the same time as Q77.3. A type 1 excludes note is for used for when two conditions cannot occur together, such as a congenital form versus an acquired form of the same condition.

Rhizomelic chondrodysplasia punctata (
ICD-10-CM Diagnosis Code E71.43
Iatrogenic carnitine deficiency
Applicable To
- Carnitine deficiency due to hemodialysis
- Carnitine deficiency due to Valproic acid therapy
E71.43
)

The following code(s) above Q77.3 contain annotation back-references

Annotation Back-References

In this context, annotation back-references refer to codes that contain:

Applicable To annotations, or
Code Also annotations, or
Code First annotations, or
Excludes1 annotations, or
Excludes2 annotations, or
Includes annotations, or
Note annotations, or
Use Additional annotations

that may be applicable to Q77.3:

Q00-Q99
2023 ICD-10-CM Range Q00-Q99
Congenital malformations, deformations and chromosomal abnormalities
Note
- Codes from this chapter are not for use on maternal records
Type 2 Excludes
- inborn errors of metabolism (E70-E88)
Congenital malformations, deformations and chromosomal abnormalities
Q77
ICD-10-CM Diagnosis Code Q77
Osteochondrodysplasia with defects of growth of tubular bones and spine
Type 1 Excludes
- mucopolysaccharidosis (E76.0-E76.3)
Type 2 Excludes
- congenital myotonic chondrodystrophy (G71.13)
Osteochondrodysplasia with defects of growth of tubular bones and spine

Clinical Information

A heterogeneous group of bone dysplasias, the common character of which is stippling of the epiphyses in infancy. The group includes a severe autosomal recessive form (chondrodysplasia punctata, rhizomelic), an autosomal dominant form (conradi-hunermann syndrome), and a milder x-linked form. Metabolic defects associated with impaired peroxisomes are present only in the rhizomelic form.
A rare congenital developmental disorder characterized by the presence of stippled foci of calcification in the hyaline cartilage, joint contractions, mental retardation and ichthyosis.

Present On Admission

POA Help

"Present On Admission" is defined as present at the time the order for inpatient admission occurs — conditions that develop during an outpatient encounter, including emergency department, observation, or outpatient surgery, are considered POA.

Q77.3 is considered exempt from POA reporting.

ICD-10-CM Q77.3 is grouped within Diagnostic Related Group(s) (MS-DRG v40.0):

564 Other musculoskeletal system and connective tissue diagnoses with mcc
565 Other musculoskeletal system and connective tissue diagnoses with cc
566 Other musculoskeletal system and connective tissue diagnoses without cc/mcc

Convert Q77.3 to ICD-9-CM

Code History

2016 (effective 10/1/2015): New code (first year of non-draft ICD-10-CM)
2017 (effective 10/1/2016): No change
2018 (effective 10/1/2017): No change
2019 (effective 10/1/2018): No change
2020 (effective 10/1/2019): No change
2021 (effective 10/1/2020): No change
2022 (effective 10/1/2021): No change
2023 (effective 10/1/2022): No change

Code annotations containing back-references to Q77.3:

Type 1 Excludes: E71.540

ICD-10-CM Diagnosis Code E71.540
Rhizomelic chondrodysplasia punctata
Type 1 Excludes
- chondrodysplasia punctata NOS (Q77.3)

Diagnosis Index entries containing back-references to Q77.3:

Chondrodysplasia Q78.9
ICD-10-CM Diagnosis Code Q78.9
Osteochondrodysplasia, unspecified
Applicable To
Chondrodystrophy NOS
Osteodystrophy NOS
- calcificans congenita Q77.3
- punctata Q77.3
Chondrodystrophy, chondrodystrophia (familial) (fetalis) (hypoplastic) Q78.9
ICD-10-CM Diagnosis Code Q78.9
Osteochondrodysplasia, unspecified
Applicable To
Chondrodystrophy NOS
Osteodystrophy NOS
- calcificans congenita Q77.3
- punctata Q77.3
Conradi Q77.3 (-Hunermann)

ICD-10-CM Codes Adjacent To Q77.3

Q76.49 Other congenital malformations of spine, not associated with scoliosis

Q76.5 Cervical rib

Q76.6 Other congenital malformations of ribs

Q76.7 Congenital malformation of sternum

Q76.8 Other congenital malformations of bony thorax

Q76.9 Congenital malformation of bony thorax, unspecified

Q77 Osteochondrodysplasia with defects of growth of tubular bones and spine

Q77.0 Achondrogenesis

Q77.1 Thanatophoric short stature

Q77.2 Short rib syndrome

Q77.3 Chondrodysplasia punctata

Q77.4 Achondroplasia

Q77.5 Diastrophic dysplasia

Q77.6 Chondroectodermal dysplasia

Q77.7 Spondyloepiphyseal dysplasia

Q77.8 Other osteochondrodysplasia with defects of growth of tubular bones and spine

Q77.9 Osteochondrodysplasia with defects of growth of tubular bones and spine, unspecified

Q78 Other osteochondrodysplasias

Q78.0 Osteogenesis imperfecta

Q78.1 Polyostotic fibrous dysplasia

Q78.2 Osteopetrosis

Reimbursement claims with a date of service on or after October 1, 2015 require the use of ICD-10-CM codes.

2023 ICD-10-CM Diagnosis Code Q77.3

Chondrodysplasia punctata

Iatrogenic carnitine deficiency

Congenital malformations, deformations and chromosomal abnormalities

Osteochondrodysplasia with defects of growth of tubular bones and spine

Rhizomelic chondrodysplasia punctata

Osteochondrodysplasia, unspecified

Osteochondrodysplasia, unspecified