ICD2022

Osteogenesis imperfecta

Code: Q78.0
Codesystem: http://hl7.org/fhir/ValueSet/icd-10

TEXT
inclusion: Fragilitas ossium

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TEXT
inclusion: Osteopsathyrosis

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Polyostotische fibröse Dysplasie [Jaffé-Lichtenstein-Syndrom]

Code: Q78.1
Codesystem: http://hl7.org/fhir/ValueSet/icd-10

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inclusion: McCune-Albright-Syndrom

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Marmorknochenkrankheit

Code: Q78.2
Codesystem: http://hl7.org/fhir/ValueSet/icd-10

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inclusion: Albers-Schönberg-Syndrom

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Progrediente diaphysäre Dysplasie

Code: Q78.3
Codesystem: http://hl7.org/fhir/ValueSet/icd-10

TEXT
inclusion: Camurati-Engelmann-Syndrom

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Enchondromatose

Code: Q78.4
Codesystem: http://hl7.org/fhir/ValueSet/icd-10

TEXT
inclusion: Maffucci-Syndrom

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TEXT
inclusion: Ollier-Krankheit

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Metaphysäre Dysplasie

Code: Q78.5
Codesystem: http://hl7.org/fhir/ValueSet/icd-10

TEXT
inclusion: Pyle-Syndrom

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Angeborene multiple Exostosen

Code: Q78.6
Codesystem: http://hl7.org/fhir/ValueSet/icd-10

TEXT
inclusion: Multiple kartilaginäre Exostosen

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Sonstige näher bezeichnete Osteochondrodysplasien

Code: Q78.8
Codesystem: http://hl7.org/fhir/ValueSet/icd-10

TEXT
inclusion: Osteopoikilie

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Osteochondrodysplasie, nicht näher bezeichnet

Code: Q78.9
Codesystem: http://hl7.org/fhir/ValueSet/icd-10

TEXT
inclusion: Chondrodystrophie o.n.A.

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TEXT
inclusion: Osteodystrophie o.n.A.

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