Chondrodysplasia pseudohermaphroditism syndrome
DOOR syndrome
Lordosis deformity of spine due to congenital skeletal dysplasia
CAGSSS - cataract, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, skeletal dysplasia syndrome
Cutis laxa with joint laxity AND retarded development
Dentinogenesis imperfecta
POF - Premature ovarian failure
Goldblatt chondrodysplasia
Abnormal development of cartilage
Chondrodysplasia, dentinogenesis imperfecta, joint laxity syndrome
Cartilage Development Disorder
chondrodystrophy
Dysplasia with defective mineralization
Hypoplastic chondrodystrophy
Suarez Stickler syndrome
Hereditary sensory neuropathy
DOORS syndrome
Cutis laxa with osteodystrophy
Skeletal dysplasia brachydactyly syndrome
Hereditary opalescent dentin
Osteochondrodysplasia syndrome (disorder)
Cartilage development disorder NOS
Deafness with onychodystrophy syndrome
Premature ovarian failure
Chondrodysplasia
Body height below reference range
Chondrodystrophy NOS
Congenital anomaly of cartilage (disorder)
Posterior sensory radicular neuropathy
Osteochondrodysplasias
Osteodystrophy (disorder)
Mononen Karnes Senac syndrome
Cataract, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, skeletal dysplasia syndrome
Nivelon Nivelon Mabille syndrome
Disorder cartilage development (NOS)
Skeletal dysplasia with wormian bone, multiple fractures, dentinogenesis imperfecta syndrome
Christian syndrome
Goldblatt syndrome
Cognitive impairment, coarse facies, heart defects, obesity, pulmonary involvement, short stature, skeletal dysplasia syndrome
Skeletal dysplasia with intellectual disability syndrome
Autosomal recessive deafness onychodystrophy syndrome
Fountain syndrome
Dysplasia with defective mineralisation
Osteodystrophy
chondrodystrophies
Congenital osteodystrophy
Deafness, onychodystrophy, osteodystrophy, intellectual disability syndrome
Hereditary growth hormone deficiency
Pure gonadal dysgenesis 46,XY
Sensory neuropathy
CHOPS syndrome
Congenital anomaly of cartilage
Chondrodysplasia with disorder of sex development syndrome
Dysplasia with decreased bone density
Osteosclerosis, ichthyosis, premature ovarian failure syndrome
Chondrodysplasia with joint dislocations gPAPP type
Ossification anomaly with psychomotor developmental delay syndrome
Osteochondrodysplasia syndrome
Genetic syndromic childhood obesity
Deafness with skeletal dysplasia and lip granuloma syndrome
Odontochondrodysplasia
Sclerosing dysplasia of bone, ichthyosis, premature ovarian failure syndrome
Swyer syndrome
Osteodystrophy NOS
osteodystrophies
Deafness, skeletal dysplasia, coarse face with full lips syndrome
Pure gonadal dysgenesis
Cutis laxa with bone dystrophy

Frequently Asked Questions

What is the ICD-10 code for osteochondrodysplasia, unspecified?

The ICD-10-CM code for osteochondrodysplasia, unspecified is Q78.9. The full clinical description is "Osteochondrodysplasia, unspecified". Q78.9 is a billable/specific code that can be used on insurance claims and medical billing.

What does ICD-10 code Q78.9 mean?

ICD-10-CM code Q78.9 represents “Osteochondrodysplasia, unspecified”. 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 Q78.9 a billable code?

Yes, Q78.9 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.

What chapter is Q78.9 in?

Q78.9 is in Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities (codes Q00-Q99).

What SNOMED CT codes does Q78.9 map to?

Q78.9 maps to 31 SNOMED CT concepts: 719800009, 1363478003, 1220595008, 764455002, 205465004, and 26 more. SNOMED CT is a clinical terminology used in electronic health records.

What are the UMLS CUIs for Q78.9?

Q78.9 is linked to 3 UMLS Concept Unique Identifiers: C0008449, C0029422, C0264009. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.

How does Q78.9 relate to ICF functioning codes?

ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like osteochondrodysplasia, unspecified affect a person's functioning — body functions, activities, participation, and environmental factors. AutoICD provides ICF Core Sets for 12+ conditions and can map clinical text to ICF categories automatically. Browse the ICF directory to explore functioning codes.

What is the ICD-11 equivalent of Q78.9?

Q78.9 maps to the ICD-11 code: LD24.Z (Syndromes with skeletal anomalies as a major feature, unspecified).

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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.