D81.819
BillableBiotin-dependent carboxylase deficiency, unspecified
Biotin-dependent carboxylase deficiency, unspecified
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Multiple carboxylase deficiency, unspecified
Includes
Conditions included under this code
- defects in the complement system
- immunodeficiency disorders, except human immunodeficiency virus [HIV] disease
- sarcoidosis
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
- autoimmune disease (systemic) NOS (M35.9)
- certain conditions originating in the perinatal period (P00-P96)
- complications of pregnancy, childbirth and the puerperium (O00-O9A)
- congenital malformations, deformations and chromosomal abnormalities (Q00-Q99)
- endocrine, nutritional and metabolic diseases (E00-E88)
- human immunodeficiency virus [HIV] disease (B20)
- injury, poisoning and certain other consequences of external causes (S00-T88)
- neoplasms (C00-D49)
- symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified (R00-R94)
Also Known As / Clinical Terms
UMLS
- Biotin-dependent carboxylase deficiencyC1389901
- Biotin-dependent carboxylase deficiency, unspecifiedC1389901
- CARBOXYLASE DEFIC COMBINEDC0026755
- CARBOXYLASE DEFIC MULTIPLEC0026755
- COMBINED CARBOXYLASE DEFICC0026755
- Carboxylase Deficiencies, CombinedC0026755
- Carboxylase Deficiencies, MultipleC0026755
- Carboxylase Deficiency, CombinedC0026755
- Carboxylase Deficiency, MultipleC0026755
- Combined Carboxylase DeficienciesC0026755
- Combined Carboxylase DeficiencyC0026755
- DEFIC COMBINED CARBOXYLASEC0026755
- DEFIC MULTIPLE CARBOXYLASEC0026755
- Deficiencies, Combined CarboxylaseC0026755
- Deficiencies, Multiple CarboxylaseC0026755
- Deficiency, Combined CarboxylaseC0026755
- Deficiency, Multiple CarboxylaseC0026755
- MULTIPLE CARBOXYLASE DEFICC0026755
- Multiple Carboxylase DeficienciesC0026755
- Multiple Carboxylase DeficiencyC0026755
- Multiple carboxylase deficiencyC0026755
- Multiple carboxylase deficiency (disorder)C0026755
- Multiple carboxylase deficiency, unspecifiedC0026755
Frequently Asked Questions
What is the ICD-10 code for biotin-dependent carboxylase deficiency, unspecified?
The ICD-10-CM code for biotin-dependent carboxylase deficiency, unspecified is D81.819. The full clinical description is "Biotin-dependent carboxylase deficiency, unspecified". D81.819 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code D81.819 mean?
ICD-10-CM code D81.819 represents "Biotin-dependent carboxylase deficiency, unspecified". It is classified under Chapter 3: Diseases of the Blood and Blood-Forming Organs and is a billable/specific code that can be used on a claim.
Is D81.819 a billable code?
Yes, D81.819 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is D81.819 in?
D81.819 is in Chapter 3: Diseases of the Blood and Blood-Forming Organs (codes D50-D89).
What codes cannot be used with D81.819?
D81.819 has Excludes1 notes indicating codes that cannot be used together with it, including: autoimmune disease (systemic) NOS (M35.9); functional disorders of polymorphonuclear neutrophils (D71); human immunodeficiency virus [HIV] disease (B20); and 2 more.
What SNOMED CT codes does D81.819 map to?
D81.819 maps to 1 SNOMED CT concept: 1172966001. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for D81.819?
D81.819 is linked to 2 UMLS Concept Unique Identifiers: C1389901, C0026755. 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.