Q99.2
BillableFragile X chromosome
Fragile X chromosome
Status
Billable / Specific
Parent Code
Q99Coding Notes
Also Known As / Clinical Terms
SNOMED CT
- FRAXA (fragile X) syndrome613003
- Fragile X syndrome613003
- Marker X syndrome613003
- Martin-Bell syndrome613003
- Fragile X chromosome205720009
- POF - Premature ovarian failure237788002
- Premature ovarian failure237788002
- Fragile X associated tremor ataxia syndrome448045004
- FRAXF syndrome716708005
- FRAXE intellectual disability syndrome716709002
- Intellectual disability associated with fragile site FRAXE716709002
- Dementia due to chromosomal anomaly722980006
- Dementia due to fragile X syndrome1259473000
- Dementia due to genetic disease1259476008
- Fragile X associated primary ovarian insufficiency1332509007
UMLS
- FRAGILE X MENTAL RETARDATION SYNDROMEC0016667
- FRAGILE X SYNDROMEC0016667
- FRAXA (fragile X) syndromeC0016667
- FXSC0016667
- Fra(X) SyndromeC0016667
- Fra(X) syndromeC0016667
- Fragile X Mental Retardation SyndromeC0016667
- Fragile X SyndromeC0016667
- Fragile X SyndromesC0016667
- Fragile X syndromeC0016667
- Fragile X syndrome (disorder)C0016667
- MARKER X SYNDROMEC0016667
- MARTIN-BELL SYNDROMEC0016667
- MENTAL RETARDATION, X-LINKED, ASSOCIATED WITH marXq28C0016667
- Marker X SyndromeC0016667
- Marker X SyndromesC0016667
- Marker X syndromeC0016667
- Martin Bell SyndromeC0016667
- Martin-Bell SyndromeC0016667
- Martin-Bell syndromeC0016667
- Mental Retardation, X-Linked, Associated With Marxq28C0016667
- Syndrome, Fragile XC0016667
- Syndrome, Marker XC0016667
- Syndrome, Martin-BellC0016667
- Syndromes, Fragile XC0016667
- Syndromes, Marker XC0016667
- X Linked Mental Retardation and MacroorchidismC0016667
- X-LINKED MENTAL RETARDATION AND MACROORCHIDISMC0016667
- X-Linked Mental Retardation and MacroorchidismC0016667
- X-linked mental retardation and macroorchidismC0016667
- autism fragile syndrome xC0016667
- disorder fragile x syndromeC0016667
- fragile X syndromeC0016667
- fragile syndrome xC0016667
- fragile x syndromeC0016667
- fragile x syndrome autismC0016667
- fragile-x syndromeC0016667
- martin bell syndromeC0016667
- martin-bell syndromeC0016667
- x fragile syndromeC0016667
- Fragile X chromosomeC0432482
- Fragile X chromosome (disorder)C0432482
- chromosome x fragileC0432482
- fragile x chromosomeC0432482
- x chromosome fragileC0432482
Frequently Asked Questions
What is the ICD-10 code for fragile x chromosome?
The ICD-10-CM code for fragile x chromosome is Q99.2. The full clinical description is "Fragile X chromosome". Q99.2 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code Q99.2 mean?
ICD-10-CM code Q99.2 represents "Fragile X chromosome". 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 Q99.2 a billable code?
Yes, Q99.2 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is Q99.2 in?
Q99.2 is in Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities (codes Q00-Q99).
What SNOMED CT codes does Q99.2 map to?
Q99.2 maps to 10 SNOMED CT concepts: 722980006, 1259473000, 1259476008, 613003, 716709002, and 5 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for Q99.2?
Q99.2 is linked to 2 UMLS Concept Unique Identifiers: C0016667, C0432482. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
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.