Q78.2
BillableOsteopetrosis
Osteopetrosis
Status
Billable / Specific
Parent Code
Q78Coding Notes
Also Known As / Clinical Terms
SNOMED CT
- Lenz-Majewski dysplasia1393001
- Lenz-Majewski hyperostosis syndrome1393001
- Osteopetrosis1926006
- Complete deafness8531006
- Sclerosteosis17568006
- Osteosclerosis49347007
- Osteochondrodysplasia with osteopetrosis50108000
- Osteopathia striata82663009
- Voorhoeve's disease82663009
- Congenital deafness95828007
- Dentin dysplasia109492001
- Dentinal dysplasia109492001
- Dentine dysplasia109492001
- Hypogammaglobulinaemia119250001
- Hypogammaglobulinemia119250001
- Osteopetrosis - delayed type205503007
- Osteopetrosis - tarda type205503007
- Functional antibody defect234556002
- Specific antibody deficiency234556002
- Specific immunoglobulin response defect234556002
- Osteopetrosis - intermediate type254121000
- CA2 - Osteopetrosis with renal tubular acidosis254122007
- Carbonic anhydrase II deficiency254122007
- Osteopetrosis with renal tubular acidosis254122007
- Osteosclerosis - Stanescu type254124008
- Axial osteosclerosis254125009
- Osteomesopycnosis254125009
- Osteomesopyknosis254125009
- Osteopathia striata with cranial sclerosis254129003
- Endosteal hyperostoses254130008
- Autosomal dominant osteosclerosis254131007
- Worth disease254131007
- Congenital hypogammaglobulinaemia267460002
- Congenital hypogammaglobulinemia267460002
- Autosomal recessive lethal osteopetrosis367489004
- Autosomal recessive malignant osteopetrosis367489004
- Congenital osteopetrosis367489004
- Infantile malignant osteopetrosis367489004
- Marble bone disease367489004
- Transient infantile osteopetrosis449777000
- Transient osteopetrosis449777000
- Colobomatous microphthalmia715771008
- Microphthalmia with colobomatous cyst715771008
- Microphthalmos co-occurrent with congenital ocular coloboma715771008
- Anhidrotic ectodermal dysplasia, immunodeficiency, osteopetrosis, lymphedema syndrome720986005
- Anhidrotic ectodermal dysplasia, immunodeficiency, osteopetrosis, lymphoedema syndrome720986005
- OL-EDA-ID (anhidrotic ectodermal dysplasia, immunodeficiency, osteopetrosis, lymphedema) syndrome720986005
- OL-EDA-ID (anhidrotic ectodermal dysplasia, immunodeficiency, osteopetrosis, lymphoedema) syndrome720986005
- Osteosclerosis, developmental delay, craniosynostosis syndrome722117000
- Infantile osteopetrosis with neuroaxonal dysplasia724226009
- Infantile osteopetrosis with neuroaxonal dysplasia syndrome724226009
- Albers Schonberg osteopetrosis725050005
- Autosomal dominant osteopetrosis type 2725050005
- Dentin dysplasia with sclerotic bone syndrome770943008
- Dentin dysplasia, sclerotic bones syndrome770943008
- Autosomal recessive osteoclast-poor osteopetrosis with hypogammaglobulinaemia773730002
- Autosomal recessive osteoclast-poor osteopetrosis with hypogammaglobulinemia773730002
- Autosomal recessive osteopetrosis type 7773730002
- Osteopetrosis hypogammaglobulinaemia syndrome773730002
- Osteopetrosis hypogammaglobulinemia syndrome773730002
- Short stature disorder due to osteosclerosis1153392009
- Osteosclerotic metaphyseal dysplasia1237513008
- Autosomal dominant osteopetrosis type 11264041000
- Pathological fracture of foot due to osteopetrosis1284897006
- COMMAD (coloboma, osteopetrosis, microphthalmia, macrocephaly, albinism, deafness) syndrome1332382002
- COMMAD syndrome1332382002
- Coloboma, osteopetrosis, microphthalmia, macrocephaly, albinism, deafness syndrome1332382002
- Pathologic fracture of right foot due to osteopetrosis220767211000119104
- Pathological fracture of left foot11309521000119101
- Pathological fracture of left foot due to osteopetrosis712365461000119105
- Pathological fracture of right foot11309481000119101
UMLS
- ALBERS SCHOENBERG DISC0029454
- Albers Schoenberg DiseaseC0029454
- Albers Schoenberg diseaseC0029454
- Albers Schonberg DiseaseC0029454
- Albers Schönberg DiseaseC0029454
- Albers-Schoenberg DiseaseC0029454
- Albers-Schonberg DiseaseC0029454
- Albers-Schonberg diseaseC0029454
- Albers-Schönberg DiseaseC0029454
- Albers-Schönberg syndromeC0029454
- Congenital OsteopetrosisC0029454
- Congenital osteopetrosisC0029454
- Disease, Albers-SchoenbergC0029454
- Disease, Albers-SchonbergC0029454
- Disease, Albers-SchönbergC0029454
- Disease, Marble BoneC0029454
- Harder, denser, fracture-prone bonesC0029454
- MARBLE BONE DISC0029454
- Marble Bone DiseaseC0029454
- Marble bone diseaseC0029454
- OsteopetrosesC0029454
- OsteopetrosisC0029454
- Osteopetrosis (disorder)C0029454
- Osteosclerosis FragilisC0029454
- Osteosclerosis Fragilis GeneralisataC0029454
- Osteosclerosis Fragilis GeneralisatasC0029454
- bone thickeningC0029454
- bones disease marbleC0029454
- bones thickeningC0029454
- congenital osteopetrosisC0029454
- marble boneC0029454
- marble bone diseaseC0029454
- marble bonesC0029454
- osteopetrosesC0029454
- osteopetrosisC0029454
- osteosclerosis fragilisC0029454
- thicken boneC0029454
- Increased bone densityC0029464
- Increased bone mineral densityC0029464
- OsteosclerosesC0029464
- OsteosclerosisC0029464
- Osteosclerosis (disorder)C0029464
- Osteosclerosis NOSC0029464
- Osteosclerosis of bonesC0029464
- osteosclerosisC0029464
Frequently Asked Questions
What is ICD-10 code Q78.2?
ICD-10-CM code Q78.2 represents "Osteopetrosis". It is a billable/specific code that can be used on a claim.
Is Q78.2 a billable code?
Yes, Q78.2 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is Q78.2 in?
Q78.2 is in Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities (codes Q00-Q99).
What SNOMED CT codes does Q78.2 map to?
Q78.2 maps to 38 SNOMED CT concepts: 725050005, 720986005, 1264041000, 254131007, 367489004, and 33 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for Q78.2?
Q78.2 is linked to 2 UMLS Concept Unique Identifiers: C0029454, C0029464. 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.