Q77.3
BillableChondrodysplasia punctata
Chondrodysplasia punctata
Status
Billable / Specific
Parent Code
Q77Coding Notes
Excludes 1
Codes that cannot be used together with this code (mutual exclusion)
- mucopolysaccharidosis (E76.0-E76.3)
- Rhizomelic chondrodysplasia punctata (E71.43)
Also Known As / Clinical Terms
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
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.
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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.