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Definition
ICD-10-CM
Code
Q78.0
Osteogenesis imperfecta
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Hierarchy
Q00-Q99
Congenital malformations, deformations and chromosomal abnormalities (Q00-Q99)
Q65-Q79
Congenital malformations and deformations of the musculoskeletal system (Q65-Q79)
Q78
Other osteochondrodysplasias
Q78.0
Osteogenesis imperfecta
Q78.1
Polyostotic fibrous dysplasia
Q78.2
Osteopetrosis
Q78.3
Progressive diaphyseal dysplasia
Q78.4
Enchondromatosis
Q78.5
Metaphyseal dysplasia
Q78.6
Multiple congenital exostoses
Q78.8
Other specified osteochondrodysplasias
Q78.9
Osteochondrodysplasia, unspecified
Notes
Q00-Q99
Codes from this chapter are not for use on maternal records
Inclusion Terms
Q78.0
Fragilitas ossium
Osteopsathyrosis
Excludes 2
Q78
congenital myotonic chondrodystrophy (G71.13)
G71.13
Myotonic chondrodystrophy
Q00-Q99
inborn errors of metabolism (E70-E88)
E70-E88
Metabolic disorders (E70-E88)
Related Terms
Adair-Dighton syndrome (brittle bones and blue sclera, deafness)
Blue sclera with fragility of bone and deafness
Brittle bones disease
Deafness (acquired) (complete) (hereditary) (partial) congenital with blue sclera and fragility of bone
Deafness (acquired) (complete) (hereditary) (partial) with blue sclera and fragility of bone
Disease, diseased Eddowes' (brittle bones and blue sclera)
Disease, diseased Lobstein's (brittle bones and blue sclera)
Disease, diseased Vrolik's (osteogenesis imperfecta)
Eddowes syndrome (-Spurway)
Ekman's syndrome (brittle bones and blue sclera)
Fragile, fragility bone, congenital (with blue sclera)
Fragilitas ossium (with blue sclerae) (hereditary)
Lobstein disease or syndrome (-Ekman)
Osteitis fragilitans
Osteogenesis imperfecta
Osteopsathyrosis (idiopathica)
Spurway's syndrome
Syndrome Adair-Dighton
Syndrome blue sclera
Syndrome Dighton's
Syndrome Eddowes'
Syndrome Ekman's
Syndrome Spurway's
Syndrome van der Hoeve's
Van der Hoeve syndrome (-de Kleyn)
Vrolik's disease