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Q78.0 - Osteogenesis imperfecta


The ICD 10 Code for Osteogenesis imperfecta is listed as Q78.0.
Additional information concerning this code and description can be found below including ICD 9 crosswalks / GEMS, chapter information, and DRGs where available.

ICD 10 CM Field Value
Diagnosis Code: Q78.0
Description: Osteogenesis imperfecta
  • Fragilitas ossium
  • Osteopsathyrosis
Diagnostic Related Groups
(MS-DRG v30.0)
456 - Spinal Fus Exc Cerv W Spinal Curv/malig/infec Or 9+ Fus W Mcc
457 - Spinal Fus Exc Cerv W Spinal Curv/malig/infec Or 9+ Fus W Cc
458 - Spinal Fus Exc Cerv W Spinal Curv/malig/infec Or 9+ Fus W/o Cc/mcc
564 - Other Musculoskeletal Sys & Connective Tissue Diagnoses W Mcc
565 - Other Musculoskeletal Sys & Connective Tissue Diagnoses W Cc
566 - Other Musculoskeletal Sys & Connective Tissue Diagnoses W/o Cc/mcc
Chapter Congenital malformations, deformations and chromosomal abnormalities (Q00-Q99)
Block Congenital malformations and deformations of the musculoskeletal system (Q65-Q79)
Parent Q78 - Other osteochondrodysplasias
ICD-9-CM Diagnosis Codes General Equivalence Mappings (GEMS):
ICD 9 Dx Code: 756.51 - Osteogenesis imperfecta
ICD-10-CM Siblings (same level / similar specificity) of Q78.0:
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