Q77.2

Billable

Short rib syndrome

Short rib syndrome

Status

Billable / Specific

Parent Code

Q77

ICD-11 Mapping

1 equivalent

Coding Notes

Inclusion Terms

Alternative clinical terms for this condition

  • Asphyxiating thoracic dysplasia [Jeune]

Excludes 1

Codes that cannot be used together with this code (mutual exclusion)

Excludes 2

Conditions not included here, but the patient may have both

Related Codes(9)
Q77.0

Achondrogenesis

BillableQ77.1

Thanatophoric short stature

BillableQ77.3

Chondrodysplasia punctata

BillableQ77.4

Achondroplasia

BillableQ77.5

Diastrophic dysplasia

BillableQ77.6

Chondroectodermal dysplasia

BillableQ77.7

Spondyloepiphyseal dysplasia

BillableQ77.8

Oth osteochndrdys w defct of growth of tublr bones and spine

BillableQ77.9

Osteochndrdys w defct of grth of tublr bones and spine, unsp

Billable
ICD-11 Equivalents(1)

ICD-11 Equivalents

View full mapping

Corresponding ICD-11 codes from the WHO crosswalk mapping

LD24.BZShort rib syndromes, unspecifiedequivalentPrimary
Also Known As / Clinical Terms(104)

SNOMED CT

UMLS

Clinical Terms

  • Familial aplasia of the vermis
  • Short rib-polydactyly syndrome, Majewski type
  • Sagittal synostosis
  • Thoracolimb dysplasia Rivera type
  • Benallegue Lacete syndrome
  • Complex craniosynostosis
  • Naumoff-type short rib polydactyly syndrome
  • Short rib polydactyly syndrome type 1
  • Short-rib syndrome, type II
  • Clover leaf skull deformity
  • Micromelia
  • Type II short rib polydactyly syndrome
  • Joubert syndrome
  • Micromelus
  • Beemer-Langer type short rib polydactyly syndrome
  • Jeune syndrome
  • Short rib dysplasia (disorder)
  • Asphyxiating thoracic dystrophy
  • Joubert syndrome with JATD (Jeune asphyxiating thoracic dystrophy)
  • Parieto-occipital craniosynostosis
  • Lambdoid craniosynostosis
  • Short rib polydactyly syndrome type 5
  • Short rib dysplasia
  • Sharma Kapoor Ramji syndrome
  • Sagittal craniosynostosis
  • Kleeblattschadel deformity
  • Saldino Noonan syndrome
  • Type IV short rib polydactyly syndrome
  • Micromelic dwarf
  • Joubert syndrome with Jeune asphyxiating thoracic dystrophy
  • Short rib polydactyly syndrome type V
  • Congenital hypoplasia of bone of pelvis
  • Jeune thoracic dysplasia
  • Type III short rib polydactyly syndrome
  • Short rib polydactyly syndrome Saldino Noonan type
  • Cloverleaf skull syndrome
  • Short rib polydactyly syndrome
  • Thoracomelic dysplasia
  • Asphyxiating thoracic dysplasia [Jeune]
  • Rivera Perez Salas syndrome
  • Thin ribs, tubular bones, dysmorphism syndrome
  • Nanomelia
  • Interparietal craniosynostosis
  • Jeune thoracic dystrophy
  • Scaphocephaly
  • Short rib polydactyly syndrome type I
  • Short rib
  • Cloverleaf skull, asphyxiating thoracic dysplasia syndrome
  • Verma-Naumoff short rib polydactyly syndrome
  • Majewski-type short rib polydactyly syndrome
Frequently Asked Questions
What is the ICD-10 code for short rib syndrome?

The ICD-10-CM code for short rib syndrome is Q77.2. The full clinical description is "Short rib syndrome". Q77.2 is a billable/specific code that can be used on insurance claims and medical billing.

What does ICD-10 code Q77.2 mean?

ICD-10-CM code Q77.2 represents “Short rib syndrome”. It is classified under Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities and is a billable/specific code that can be used on a claim.

Is Q77.2 a billable code?

Yes, Q77.2 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.

What chapter is Q77.2 in?

Q77.2 is in Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities (codes Q00-Q99).

What codes cannot be used with Q77.2?

Q77.2 has Excludes1 notes indicating codes that cannot be used together with it, including: mucopolysaccharidosis (E76.0-E76.3).

What SNOMED CT codes does Q77.2 map to?

Q77.2 maps to 21 SNOMED CT concepts: 75049004, 254052001, 783181006, 254022009, 8611000119100, and 16 more. SNOMED CT is a clinical terminology used in electronic health records.

What are the UMLS CUIs for Q77.2?

Q77.2 is linked to 2 UMLS Concept Unique Identifiers: C2910340, C0432195. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.

How does Q77.2 relate to ICF functioning codes?

ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like short rib syndrome affect a person's functioning: body functions, activities, participation, and environmental factors. AutoICD provides ICF Core Sets for 12+ conditions and can map clinical text to ICF categories automatically. Browse the ICF directory to explore functioning codes.

What is the ICD-11 equivalent of Q77.2?

Q77.2 maps to the ICD-11 code: LD24.BZ (Short rib syndromes, unspecified).

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Includes SNOMED Clinical Terms® (SNOMED CT®) used by permission of SNOMED International. Includes content from the UMLS Metathesaurus, courtesy of the U.S. National Library of Medicine.