Q77.2
BillableShort rib syndrome
Short rib syndrome
Status
Billable / Specific
Parent Code
Q77Coding 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)
- mucopolysaccharidosis (E76.0-E76.3)
Also Known As / Clinical Terms
SNOMED CT
- Majewski-type short rib polydactyly syndrome72922008
- Short rib-polydactyly syndrome, Majewski type72922008
- Short-rib syndrome, type II72922008
- Type II short rib polydactyly syndrome72922008
- Micromelia74370006
- Micromelic dwarf74370006
- Micromelus74370006
- Nanomelia74370006
- Asphyxiating thoracic dystrophy75049004
- Jeune syndrome75049004
- Jeune thoracic dysplasia75049004
- Jeune thoracic dystrophy75049004
- Lambdoid craniosynostosis109417006
- Parieto-occipital craniosynostosis109417006
- Interparietal craniosynostosis109418001
- Sagittal craniosynostosis109418001
- Sagittal synostosis109418001
- Scaphocephaly109418001
- Short rib polydactyly syndrome205484001
- Short rib249696007
- Familial aplasia of the vermis253175003
- Clover leaf skull deformity254022009
- Cloverleaf skull syndrome254022009
- Kleeblattschadel deformity254022009
- Short rib dysplasia254050009
- Short rib syndrome254050009
- Naumoff-type short rib polydactyly syndrome254051008
- Type III short rib polydactyly syndrome254051008
- Verma-Naumoff short rib polydactyly syndrome254051008
- Beemer-Langer type short rib polydactyly syndrome254052001
- Type IV short rib polydactyly syndrome254052001
- Joubert syndrome716997004
- Saldino Noonan syndrome726032008
- Short rib polydactyly syndrome Saldino Noonan type726032008
- Short rib polydactyly syndrome type 1726032008
- Short rib polydactyly syndrome type I726032008
- Joubert syndrome with JATD (Jeune asphyxiating thoracic dystrophy)733418003
- Joubert syndrome with Jeune asphyxiating thoracic dystrophy733418003
- Rivera Perez Salas syndrome783003009
- Thoracolimb dysplasia Rivera type783003009
- Thoracomelic dysplasia783003009
- Sharma Kapoor Ramji syndrome783004003
- Thin ribs, tubular bones, dysmorphism syndrome783004003
- Benallegue Lacete syndrome783181006
- Cloverleaf skull, asphyxiating thoracic dysplasia syndrome783181006
- Congenital hypoplasia of bone of pelvis1145432000
- Short rib polydactyly syndrome type 51279843003
- Short rib polydactyly syndrome type V1279843003
- Complex craniosynostosis8611000119100
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.
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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.