Q77.3
BillableChondrodysplasia punctata
Chondrodysplasia punctata
Coding Notes
Excludes 1
Codes that cannot be used together with this code (mutual exclusion)
Excludes 2
Conditions not included here, but the patient may have both
Related Codes(9)
Q77.0Achondrogenesis
Q77.1Thanatophoric short stature
Q77.2Short rib syndrome
Q77.4Achondroplasia
Q77.5Diastrophic dysplasia
Q77.6Chondroectodermal dysplasia
Q77.7Spondyloepiphyseal dysplasia
Q77.8Oth osteochndrdys w defct of growth of tublr bones and spine
Q77.9Osteochndrdys w defct of grth of tublr bones and spine, unsp
ICD-11 Equivalents(1)
ICD-11 Equivalents
View full mappingCorresponding ICD-11 codes from the WHO crosswalk mapping
Also Known As / Clinical Terms(68)
SNOMED CT
- Hyperphosphatasia-osteoectasia syndrome76556008
- Disorder of cholesterol metabolism123963007
- Disorder of cholesterol synthesis238036004
- Chondrodysplasia punctata, X-linked recessive type254082007
- Chondrodysplasia punctata, MT type254083002
- Chondrodysplasia punctata, tibia-metacarpal type254083002
- Chondrodysplasia punctata278715001
- Chondrodysplasia punctata (stippled epiphyses) group278715001
- Lethal chondrodysplasia with fragmented bone389260001
- Greenberg dysplasia389261002
- Chondrodysplasia calcificans congenita398719004
- Chondrodysplasia punctata, Conradi-Hunermann type398719004
- Chondrodysplasia punctata, Conradi-Hünermann type398719004
- Conradi disease398719004
- Conradi's syndrome398719004
- Conradi-Hunermann syndrome398719004
- Conradi-Hünermann syndrome398719004
- Chondrodysplasia punctata, X-linked dominant type398958000
- Chondrodystrophia calcificans congenita398958000
- Conradi Hünermann Happle syndrome398958000
- Happle syndrome398958000
- X-linked chondrodysplasia punctata type 2398958000
- Chondrodysplasia punctata Toriello type715631005
- Toriello Higgins Miller syndrome715631005
- BCDP - brachytelephalangic chondrodysplasia punctata778067002
- Brachytelephalangic chondrodysplasia punctata778067002
- Chondrodysplasia punctata due to maternal autoimmune disease890437007
UMLS
- CHONDRODYSTROPHIA CALCIFICANS CONGENC0008445
- Chondrodysplasia PunctataC0008445
- Chondrodysplasia punctataC0008445
- Chondrodysplasia punctata (stippled epiphyses) groupC0008445
- Chondrodysplasia punctata (stippled epiphyses) group (disorder)C0008445
- Chondrodystrophia Calcificans CongenitaC0008445
- Dysplasia Epiphysialis PunctataC0008445
- Epiphyses, StippledC0008445
- Stippled EpiphysesC0008445
- chondrodysplasia punctataC0008445
Clinical Terms
- Chondrodysplasia punctata due to maternal autoimmune disease
- Disorder of cholesterol metabolism
- Epiphyses, Stippled
- Dysplasia Epiphysialis Punctata
- Conradi Hünermann Happle syndrome
- Conradi's syndrome
- Conradi-Hunermann syndrome
- Chondrodysplasia punctata Toriello type
- Conradi-Hünermann syndrome
- Chondrodysplasia punctata, Conradi-Hunermann type
- X-linked chondrodysplasia punctata type 2
- Chondrodysplasia punctata, X-linked dominant type
- Chondrodysplasia punctata (stippled epiphyses) group
- Chondrodysplasia punctata, MT type
- Chondrodysplasia punctata, Conradi-Hünermann type
- Brachytelephalangic chondrodysplasia punctata
- Chondrodysplasia calcificans congenita
- Toriello Higgins Miller syndrome
- Chondrodystrophia calcificans congenita
- Hyperphosphatasia-osteoectasia syndrome
- Happle syndrome
- BCDP - brachytelephalangic chondrodysplasia punctata
- Greenberg dysplasia
- Chondrodysplasia punctata (stippled epiphyses) group (disorder)
- CHONDRODYSTROPHIA CALCIFICANS CONGEN
- Lethal chondrodysplasia with fragmented bone
- Disorder of cholesterol synthesis
- Stippled Epiphyses
- Chondrodysplasia punctata, X-linked recessive type
- Conradi disease
- Chondrodysplasia punctata, tibia-metacarpal type
Frequently Asked Questions
What is the ICD-10 code for chondrodysplasia punctata?
The ICD-10-CM code for chondrodysplasia punctata is Q77.3. The full clinical description is "Chondrodysplasia punctata". Q77.3 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code Q77.3 mean?
ICD-10-CM code Q77.3 represents “Chondrodysplasia punctata”. 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 Q77.3 a billable code?
Yes, Q77.3 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is Q77.3 in?
Q77.3 is in Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities (codes Q00-Q99).
What codes cannot be used with Q77.3?
Q77.3 has Excludes1 notes indicating codes that cannot be used together with it, including: mucopolysaccharidosis (E76.0-E76.3); Rhizomelic chondrodysplasia punctata (E71.43).
What SNOMED CT codes does Q77.3 map to?
Q77.3 maps to 13 SNOMED CT concepts: 778067002, 398719004, 278715001, 715631005, 890437007, and 8 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for Q77.3?
Q77.3 is linked to 1 UMLS Concept Unique Identifier: C0008445. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
How does Q77.3 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like chondrodysplasia punctata 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 Q77.3?
Q77.3 maps to the ICD-11 code: LD24.04 (Chondrodysplasia punctata).
Automate ICD-10 Coding With AI
Send clinical text to the AutoICD API and get back structured ICD-10 codes with confidence scores. Integrates into any EHR or billing system in minutes.
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.