Q99.9
BillableChromosomal abnormality, unspecified
Chromosomal abnormality, unspecified
Status
Billable / Specific
Parent Code
Q99Coding Notes
Also Known As / Clinical Terms
SNOMED CT
- Autosomal hereditary disorder1899006
- Anomaly of chromosome pair 102893009
- Anomaly of chromosome pair 95051002
- Anomaly of chromosome pair 209839007
- AD - Autosomal dominant11164009
- Autosomal dominant hereditary disorder11164009
- Anomaly of chromosome pair 313674001
- Anomaly of chromosome pair 1516569009
- Anomaly of chromosome pair 1317760001
- Anomaly of chromosome pair 1427183007
- Anomaly of chromosome pair 1732107005
- Anomaly of chromosome pair 232299009
- Anomaly of chromosome pair 737367006
- Anomaly of chromosome pair 1237535007
- Anomaly of chromosome pair 644710007
- Anomaly of chromosome pair 848082007
- Anomaly of chromosome pair 1653392002
- Anomaly of chromosome pair 557361003
- Anomaly of chromosome pair 1859033006
- Anomaly of chromosome pair 1160891003
- Anomaly of chromosome pair 2170156005
- Anomaly of chromosome pair 2270452003
- Anomaly of chromosome74345006
- Chromosomal abnormality syndrome74345006
- Chromosomal hereditary disorder74345006
- Chromosomal imbalance syndrome74345006
- Chromosomopathy74345006
- Congenital chromosomal disease74345006
- Congenital disorder due to abnormality of chromosome number OR structure74345006
- Anomaly of chromosome pair 174769007
- Anomaly of chromosome pair 1979656000
- Anomaly of chromosome pair 484711007
- Autosomal recessive hereditary disorder85995004
- Hereditary disorder trait (autosomal)85995004
- Recessive hereditary disorder (autosomal)85995004
- Dominant autosomal hereditary disorder, complete penetrance86426007
- Dominant autosomal hereditary disorder, incomplete penetrance87006007
- Immunodeficiency associated with chromosomal abnormality234632005
- Autosomal chromosomal disorder403759001
- Chromosomal anomaly409709004
- Chromosomal disorder409709004
- Cardiac arrhythmia associated with genetic disorder698270004
- Schinzel syndrome700211007
- Ulnar mammary syndrome700211007
- Ulnar-mammary syndrome700211007
- ALPS - autoimmune lymphoproliferative syndrome702444009
- Autoimmune lymphoproliferative syndrome702444009
- Canale-Smith syndrome702444009
- Autosomal translocation709418005
- Dementia due to chromosomal anomaly722980006
- Deletion of part of short arm of chromosome 16726388008
- ATR-16 syndrome734349003
- Alpha thalassaemia intellectual disability syndrome, deletion type734349003
- Alpha thalassemia intellectual disability syndrome, deletion type734349003
- Alpha-thalassaemia intellectual disability syndrome linked to chromosome 16734349003
- Alpha-thalassemia intellectual disability syndrome linked to chromosome 16734349003
- Genetic disease782964007
- Autoimmune lymphoproliferative syndrome due to CTLA4 haploinsufficiency1197361002
- Autoimmune lymphoproliferative syndrome due to cytotoxic T-lymphocyte associated protein 4 haploinsufficiency1197361002
- CTLA-4 haploinsufficiency with autoimmune infiltration disease1197361002
- Dementia due to genetic disease1259476008
- CFTR (cystic fibrosis transmembrane conductance regulator) related disorder1335845008
- CFTR-related disorder1335845008
- Cystic fibrosis transmembrane conductance regulator-related disorder1335845008
UMLS
- Anomaly of chromosomeC0008626
- CHROMOSOMAL DISC0008626
- CHROMOSOME ABNORM DISC0008626
- CHROMOSOME DISC0008626
- Chromosomal DisorderC0008626
- Chromosomal DisordersC0008626
- Chromosomal abnormality NOSC0008626
- Chromosomal abnormality syndromeC0008626
- Chromosomal abnormality, unspecifiedC0008626
- Chromosomal anomaliesC0008626
- Chromosomal anomalyC0008626
- Chromosomal disorderC0008626
- Chromosomal disorder (disorder)C0008626
- Chromosomal hereditary disorderC0008626
- Chromosomal imbalance syndromeC0008626
- Chromosome Abnormality DisorderC0008626
- Chromosome Abnormality DisordersC0008626
- Chromosome DisorderC0008626
- Chromosome DisordersC0008626
- Chromosome abnormalityC0008626
- Chromosome disorderC0008626
- ChromosomopathyC0008626
- Conditions due to anomaly of unspecified chromosomeC0008626
- Congenital chromosomal diseaseC0008626
- Congenital disorder due to abnormality of chromosome number OR structureC0008626
- Congenital disorder due to abnormality of chromosome number OR structure (disorder)C0008626
- Cytogenetic abnormalityC0008626
- Disorder, ChromosomalC0008626
- Disorder, ChromosomeC0008626
- Disorder, Chromosome AbnormalityC0008626
- Disorders, ChromosomalC0008626
- Disorders, ChromosomeC0008626
- abnormalities chromosomesC0008626
- abnormality chromosomalC0008626
- abnormality chromosomeC0008626
- anomalies chromosomeC0008626
- anomalies chromosomesC0008626
- anomaly chromosomalC0008626
- chromosomal abnormalityC0008626
- chromosomal anomaliesC0008626
- chromosomal diseaseC0008626
- chromosomal diseasesC0008626
- chromosomal disorderC0008626
- chromosomal disordersC0008626
- chromosome abnormalityC0008626
- chromosome anomalyC0008626
- chromosome disorderC0008626
- chromosome disordersC0008626
- chromosomes disorderC0008626
- chromosomes disordersC0008626
- diseases chromosomalC0008626
- disorders chromosomeC0008626
Frequently Asked Questions
What is the ICD-10 code for chromosomal abnormality, unspecified?
The ICD-10-CM code for chromosomal abnormality, unspecified is Q99.9. The full clinical description is "Chromosomal abnormality, unspecified". Q99.9 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code Q99.9 mean?
ICD-10-CM code Q99.9 represents "Chromosomal abnormality, 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 Q99.9 a billable code?
Yes, Q99.9 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is Q99.9 in?
Q99.9 is in Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities (codes Q00-Q99).
What SNOMED CT codes does Q99.9 map to?
Q99.9 maps to 42 SNOMED CT concepts: 11164009, 702444009, 734349003, 74345006, 74769007, and 37 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for Q99.9?
Q99.9 is linked to 1 UMLS Concept Unique Identifier: C0008626. 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.