D64.0
BillableHereditary sideroblastic anemia
Hereditary sideroblastic anemia
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Sex-linked hypochromic sideroblastic anemia
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
SNOMED CT
- X chromosome-linked sideroblastic anaemia48983004
- X chromosome-linked sideroblastic anemia48983004
- X-linked sideroblastic anaemia48983004
- X-linked sideroblastic anemia48983004
- Autosomal recessive sideroblastic anaemia717050005
- Autosomal recessive sideroblastic anemia717050005
- X-linked sideroblastic anaemia with spinocerebellar ataxia719816006
- X-linked sideroblastic anemia with spinocerebellar ataxia719816006
- Adult-onset autosomal recessive sideroblastic anaemia720465002
- Adult-onset autosomal recessive sideroblastic anemia720465002
- GLRX5 (glutaredoxin 5) related sideroblastic anaemia720465002
- GLRX5 (glutaredoxin 5) related sideroblastic anemia720465002
- Mitochondrial myopathy with sideroblastic anaemia syndrome724138007
- Mitochondrial myopathy with sideroblastic anemia syndrome724138007
- Myopathy, lactic acidosis and sideroblastic anaemia724138007
- Myopathy, lactic acidosis and sideroblastic anemia724138007
- Severe congenital hypochromic anaemia with ringed sideroblasts725463007
- Severe congenital hypochromic anemia with ringed sideroblasts725463007
- Severe congenital hypochromic sideroblastic anaemia725463007
- Severe congenital hypochromic sideroblastic anemia725463007
- Congenital sideroblastic anaemia, B-cell immunodeficiency, periodic fever, developmental delay syndrome765327005
- Congenital sideroblastic anemia, B-cell immunodeficiency, periodic fever, developmental delay syndrome765327005
- Autosomal dominant sideroblastic anaemia1148914007
- Autosomal dominant sideroblastic anemia1148914007
UMLS
- ANEMIA, HYPOCHROMICC4551511
- ANEMIA, HEREDITARY SIDEROBLASTICC4551511
- ANEMIA, SIDEROBLASTIC, 1C4551511
- ANEMIA, SIDEROBLASTIC, X-LINKEDC4551511
- ANH1C4551511
- Anemia, Hereditary SideroblasticC4551511
- Anemia, Sex-Linked Hypochromic SideroblasticC4551511
- Anemia, Sideroblastic, X-LinkedC4551511
- Anemia, sex-linked hypochromic sideroblasticC4551511
- Congenital Sideroblastic AnaemiaC4551511
- Erythroid 5-Aminolevulinate Synthase DeficiencyC4551511
- Erythroid 5-aminolevulinate synthase deficiencyC4551511
- HEREDITARY IRON-LOADING ANEMIAC4551511
- Hereditary Iron-Loading AnemiaC4551511
- SIDBA1C4551511
- Sex-linked hypochromic sideroblastic anemiaC4551511
- X Chromosome-Linked Sideroblastic AnemiaC4551511
- X chromosome-linked sideroblastic anaemiaC4551511
- X chromosome-linked sideroblastic anemiaC4551511
- X chromosome-linked sideroblastic anemia (disorder)C4551511
- X-Linked Pyridoxine-Responsive Sideroblastic AnemiaC4551511
- X-linked pyridoxine-responsive sideroblastic anemiaC4551511
- X-linked sideroblastic anaemiaC4551511
- X-linked sideroblastic anemiaC4551511
- XLSAC4551511
- Anemia, hereditary sideroblasticC0221018
- Congenital sideroblastic anaemiaC0221018
- Hereditary Sideroblastic AnemiaC0221018
- Hereditary iron-loading anemiaC0221018
- Hereditary sideroblastic anaemiaC0221018
- Hereditary sideroblastic anemiaC0221018
Frequently Asked Questions
What is ICD-10 code D64.0?
ICD-10-CM code D64.0 represents "Hereditary sideroblastic anemia". It is a billable/specific code that can be used on a claim.
Is D64.0 a billable code?
Yes, D64.0 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is D64.0 in?
D64.0 is in Chapter 3: Diseases of the Blood and Blood-Forming Organs (codes D50-D89).
What codes cannot be used with D64.0?
D64.0 has Excludes1 notes indicating codes that cannot be used together with it, including: refractory anemia (D46.-); refractory anemia with excess blasts in transformation [RAEB T] (C92.0-).
What SNOMED CT codes does D64.0 map to?
D64.0 maps to 8 SNOMED CT concepts: 720465002, 1148914007, 717050005, 765327005, 724138007, and 3 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for D64.0?
D64.0 is linked to 2 UMLS Concept Unique Identifiers: C4551511, C0221018. 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.