Q78.6
BillableMultiple congenital exostoses
Multiple congenital exostoses
Status
Billable / Specific
Parent Code
Q78Coding Notes
Also Known As / Clinical Terms
SNOMED CT
- Anetoderma238828009
- Atrophoderma maculatum238828009
- Diaphyseal aclasia254044004
- Hereditary multiple exostosis254044004
- Multiple congenital exostosis254044004
- Multiple exostoses type I254044004
- Multiple osteochondromatosis254044004
- Osteochondromatosis254044004
- Osteochondromatosis syndrome254044004
- Congenital exostosis268276007
- Disorder characterised by multiple exostoses410063006
- Disorder characterized by multiple exostoses410063006
- Exostosis, anetoderma, brachydactyly type E syndrome733416004
- Exostosis, anetodermia, brachydactyly type E syndrome733416004
UMLS
- Aclases, DiaphysealC0015306
- Aclasis, DiaphysealC0015306
- Bessel-Hagen DiseaseC0015306
- Bessel-Hagen diseaseC0015306
- Cartilaginous Exostoses, MultipleC0015306
- Cartilaginous Exostosis, MultipleC0015306
- Chondrodysplasia, Hereditary DeformingC0015306
- Chondrodysplasias, Hereditary DeformingC0015306
- DIAPHYSEAL ACLASISC0015306
- Deforming Chondrodysplasia, HereditaryC0015306
- Deforming Chondrodysplasias, HereditaryC0015306
- Diaphyseal AclasesC0015306
- Diaphyseal AclasisC0015306
- Diaphyseal aclasiaC0015306
- Diaphyseal aclasisC0015306
- EXOSTOSES, MULTIPLE, TYPE IC0015306
- EXTC0015306
- EXT1C0015306
- Exostoses, FamilialC0015306
- Exostoses, Hereditary MultipleC0015306
- Exostoses, MultipleC0015306
- Exostoses, Multiple CartilaginousC0015306
- Exostoses, Multiple HereditaryC0015306
- Exostoses, Multiple, Type IC0015306
- Exostoses, multiple hereditaryC0015306
- Exostosis, FamilialC0015306
- Exostosis, Hereditary MultipleC0015306
- Exostosis, MultipleC0015306
- Exostosis, Multiple CartilaginousC0015306
- Familial ExostosesC0015306
- Familial ExostosisC0015306
- Familial exostosesC0015306
- Hereditary Deforming ChondrodysplasiaC0015306
- Hereditary Deforming ChondrodysplasiasC0015306
- Hereditary Exostoses, MultipleC0015306
- Hereditary Multiple ExostosesC0015306
- Hereditary Multiple ExostosisC0015306
- Hereditary multiple exostosesC0015306
- Hereditary multiple exostosisC0015306
- Hereditary multiple osteochondromasC0015306
- MULTIPLE CARTILAGINOUS EXOSTOSESC0015306
- MULTIPLE OSTEOCHONDROMASC0015306
- Multiple Cartilaginous ExostosesC0015306
- Multiple Cartilaginous ExostosisC0015306
- Multiple ExostosesC0015306
- Multiple Exostoses, HereditaryC0015306
- Multiple ExostosisC0015306
- Multiple Exostosis, HereditaryC0015306
- Multiple Hereditary ExostosesC0015306
- Multiple OsteochondromaC0015306
- Multiple OsteochondromasC0015306
- Multiple OsteochondromatosisC0015306
- Multiple congenital exostosesC0015306
- Multiple congenital exostosisC0015306
- Multiple congenital exostosis (disorder)C0015306
- Multiple exostosesC0015306
- Multiple exostoses type IC0015306
- Multiple hereditary exostosesC0015306
- Multiple hereditary exostosisC0015306
- Multiple osteochondromatosisC0015306
- OSTEOCHONDROMATOSISC0015306
- Osteochondroma, MultipleC0015306
- Osteochondromas, MultipleC0015306
- OsteochondromatosisC0015306
- Osteochondromatosis syndromeC0015306
- diaphyseal aclasesC0015306
- diaphyseal aclasisC0015306
- hereditary exostosis multipleC0015306
- hereditary multiple exostosesC0015306
- hereditary multiple exostosisC0015306
- multiple cartilaginous exostosesC0015306
- multiple cartilaginous exostosisC0015306
- multiple exostosesC0015306
- multiple exostosisC0015306
- multiple exostosis syndromeC0015306
- multiple hereditary exostosesC0015306
- multiple hereditary exostosisC0015306
- multiple osteochondromaC0015306
- multiple osteochondromasC0015306
- multiple osteochondromatosisC0015306
Frequently Asked Questions
What is the ICD-10 code for multiple congenital exostoses?
The ICD-10-CM code for multiple congenital exostoses is Q78.6. The full clinical description is "Multiple congenital exostoses". Q78.6 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code Q78.6 mean?
ICD-10-CM code Q78.6 represents "Multiple congenital exostoses". 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 Q78.6 a billable code?
Yes, Q78.6 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is Q78.6 in?
Q78.6 is in Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities (codes Q00-Q99).
What SNOMED CT codes does Q78.6 map to?
Q78.6 maps to 5 SNOMED CT concepts: 238828009, 268276007, 254044004, 410063006, 733416004. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for Q78.6?
Q78.6 is linked to 1 UMLS Concept Unique Identifier: C0015306. 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.