Q78.9
BillableOsteochondrodysplasia, unspecified
Osteochondrodysplasia, unspecified
Status
Billable / Specific
Parent Code
Q78Coding Notes
Also Known As / Clinical Terms
SNOMED CT
- Hypoplastic chondrodystrophy1418007
- Hereditary sensory neuropathy11442006
- Posterior sensory radicular neuropathy11442006
- Osteodystrophy12010005
- Cutis laxa with bone dystrophy73856006
- Cutis laxa with joint laxity AND retarded development73856006
- Cutis laxa with osteodystrophy73856006
- Pure gonadal dysgenesis 46,XY95218005
- Swyer syndrome95218005
- Pure gonadal dysgenesis95219002
- Sensory neuropathy95662005
- Osteochondrodysplasia syndrome105985007
- Dentinogenesis imperfecta196286005
- Hereditary opalescent dentin196286005
- Chondrodysplasia205465004
- POF - Premature ovarian failure237788002
- Premature ovarian failure237788002
- Dysplasia with decreased bone density254104009
- Dysplasia with defective mineralisation254117007
- Dysplasia with defective mineralization254117007
- Chondrodysplasia, dentinogenesis imperfecta, joint laxity syndrome717823001
- Goldblatt chondrodysplasia717823001
- Goldblatt syndrome717823001
- Odontochondrodysplasia717823001
- Autosomal recessive deafness onychodystrophy syndrome719800009
- DOOR syndrome719800009
- DOORS syndrome719800009
- Deafness, onychodystrophy, osteodystrophy, intellectual disability syndrome719800009
- Chondrodysplasia pseudohermaphroditism syndrome720851007
- Chondrodysplasia with disorder of sex development syndrome720851007
- Nivelon Nivelon Mabille syndrome720851007
- Deafness with skeletal dysplasia and lip granuloma syndrome720957007
- Deafness, skeletal dysplasia, coarse face with full lips syndrome720957007
- Fountain syndrome720957007
- Ossification anomaly with psychomotor developmental delay syndrome722107005
- Osteosclerosis, ichthyosis, premature ovarian failure syndrome722114007
- Sclerosing dysplasia of bone, ichthyosis, premature ovarian failure syndrome722114007
- Christian syndrome722478008
- Skeletal dysplasia with intellectual disability syndrome722478008
- Mononen Karnes Senac syndrome733095006
- Skeletal dysplasia brachydactyly syndrome733095006
- Skeletal dysplasia with wormian bone, multiple fractures, dentinogenesis imperfecta syndrome733468006
- Suarez Stickler syndrome733468006
- CHOPS syndrome764455002
- Cognitive impairment, coarse facies, heart defects, obesity, pulmonary involvement, short stature, skeletal dysplasia syndrome764455002
- Deafness with onychodystrophy syndrome773735007
- Chondrodysplasia with joint dislocations gPAPP type782882009
- Hereditary growth hormone deficiency1186807002
- Lordosis deformity of spine due to congenital skeletal dysplasia1187362007
- CAGSSS - cataract, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, skeletal dysplasia syndrome1220595008
- Cataract, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, skeletal dysplasia syndrome1220595008
- Genetic syndromic childhood obesity1359763002
- Body height below reference range1363478003
- Congenital osteodystrophy5731000119108
UMLS
- Abnormal development of cartilageC0008449
- Cartilage Development DisorderC0008449
- Cartilage development disorderC0008449
- Cartilage development disorder NOSC0008449
- ChondrodystrophyC0008449
- Chondrodystrophy NOSC0008449
- Congenital anomaly of cartilageC0008449
- Congenital anomaly of cartilage (disorder)C0008449
- Disorder cartilage development (NOS)C0008449
- chondrodystrophiesC0008449
- chondrodystrophyC0008449
- OsteochondrodysplasiaC0029422
- Osteochondrodysplasia syndromeC0029422
- Osteochondrodysplasia syndrome (disorder)C0029422
- Osteochondrodysplasia, unspecifiedC0029422
- OsteochondrodysplasiasC0029422
- OsteodystrophyC0264009
- Osteodystrophy (disorder)C0264009
- Osteodystrophy NOSC0264009
- osteodystrophiesC0264009
- osteodystrophyC0264009
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.
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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.