D56.1
BillableBeta thalassemia
Beta thalassemia
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Beta thalassemia major
- Cooley's anemia
- Homozygous beta thalassemia
- Severe beta thalassemia
- Thalassemia intermedia
- Thalassemia major
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
- Thalassaemia intermedia934007
- Thalassemia intermedia934007
- A gamma beta^+^ hereditary persistence of fetal hemoglobin AND beta^0^ thalassemia in cis5967006
- A>gamma< beta^+^ HPFH AND beta^0^ thalassaemia in cis5967006
- A>gamma< beta^+^ HPFH AND beta^0^ thalassemia in cis5967006
- beta^+^ Thalassaemia, normal Hb A>2<, type 215326009
- beta^+^ Thalassemia, normal Hb A>2<, type 215326009
- HPFH (hereditary persistence of fetal haemoglobin) beta-thalassaemia syndrome16964007
- HPFH (hereditary persistence of fetal hemoglobin) beta-thalassemia syndrome16964007
- Hereditary persistence of fetal haemoglobin thalassaemia16964007
- Hereditary persistence of fetal hemoglobin thalassemia16964007
- Hereditary persistence of foetal haemoglobin thalassaemia16964007
- Beta thalassaemia major26682008
- Cooley's anaemia26682008
- Cooley's anemia26682008
- Homozygous beta thalassaemia26682008
- Homozygous beta thalassemia26682008
- Mediterranean anemia26682008
- Beta 0 thalassaemia deletion type27080008
- Beta 0 thalassemia deletion type27080008
- Beta zero thalassaemia deletion type27080008
- Beta zero thalassemia deletion type27080008
- Haemoglobin S-F disease36472007
- Hemoglobin S-F disease36472007
- Microdrepanocytic disease36472007
- Microdrepanocytosis36472007
- Sickle cell thalassaemia disease36472007
- Sickle cell thalassemia disease36472007
- Sickle cell-thalassaemia disease36472007
- Sickle cell-thalassemia disease36472007
- Thalassaemia-haemoglobin S disease36472007
- Thalassemia-hemoglobin S disease36472007
- HPFH A gamma beta^+^ thalassaemia39586009
- HPFH A gamma beta^+^ thalassemia39586009
- Hereditary persistence of fetal haemoglobin A gamma beta^+^ thalassaemia39586009
- Hereditary persistence of fetal hemoglobin (HPFH) A gamma beta^+^ thalassemia39586009
- Hereditary persistence of fetal hemoglobin A gamma beta^+^ thalassemia39586009
- Hereditary persistence of foetal haemoglobin (HPFH) A gamma beta^+^ thalassaemia39586009
- Beta plus thalassaemia normal haemoglobin A>2< type 1 silent47084006
- Beta plus thalassemia normal hemoglobin A>2< type 1 silent47084006
- HPFH (hereditary persistence of fetal haemoglobin) G gamma beta plus thalassaemia61395005
- HPFH (hereditary persistence of fetal hemoglobin) G gamma beta plus thalassemia61395005
- HPFH (hereditary persistence of foetal haemoglobin) G gamma beta plus thalassaemia61395005
- Hereditary persistence of fetal haemoglobin G gamma beta plus thalassaemia61395005
- Hereditary persistence of fetal hemoglobin G gamma beta plus thalassemia61395005
- Beta thalassaemia65959000
- Beta thalassaemia syndrome65959000
- Beta thalassemia65959000
- Beta thalassemia syndrome65959000
- beta thalassaemia65959000
- beta thalassemia65959000
- Homozygous thalassaemia75451007
- Homozygous thalassemia75451007
- Thalassaemia major75451007
- Thalassemia major75451007
- Beta plus thalassaemia79592006
- Beta plus thalassemia79592006
- beta plus thalassaemia79592006
- beta plus thalassemia79592006
- Beta 0 thalassaemia86715000
- Beta 0 thalassemia86715000
- Beta zero thalassaemia86715000
- Beta zero thalassemia86715000
- beta zero thalassaemia86715000
- beta zero thalassemia86715000
- Beta 0 thalassaemia non deletion type111572002
- Beta 0 thalassemia non deletion type111572002
- Beta zero thalassaemia non deletion type111572002
- Beta zero thalassemia non deletion type111572002
- Double heterozygous for Hb S and beta thalassaemia127041004
- Double heterozygous for Hb S and beta thalassemia127041004
- Haemoglobin S/beta thalassaemia127041004
- Hemoglobin S/beta thalassemia127041004
- Sickle cell-beta-thalassaemia127041004
- Sickle cell-beta-thalassemia127041004
- Thalassaemia with haemoglobin S disease127041004
- Thalassemia with hemoglobin S disease127041004
- Sickle cell beta plus thalassaemia127042006
- Sickle cell beta plus thalassemia127042006
- Beta thalassaemia intermedia191189009
- Beta thalassemia intermedia191189009
- Dominant beta-thalassaemia716682000
- Dominant beta-thalassemia716682000
- Inclusion body beta-thalassaemia716682000
- Inclusion body beta-thalassemia716682000
- Beta thalassaemia X-linked thrombocytopenia syndrome718196002
- Beta thalassemia X-linked thrombocytopenia syndrome718196002
- Beta thalassaemia major in mother complicating pregnancy153202341000119106
- Beta thalassemia major in mother complicating pregnancy153202341000119106
UMLS
- Anemia, CooleyC0002875
- Anemia, Cooley'sC0002875
- Anemia, CooleysC0002875
- Anemia, ErythroblasticC0002875
- Anemia, MediterraneanC0002875
- Anemias, ErythroblasticC0002875
- Anemias, MediterraneanC0002875
- Beta Thalassemia MajorC0002875
- Beta thalassaemia majorC0002875
- Beta thalassemia majorC0002875
- Cooley AnemiaC0002875
- Cooley's AnemiaC0002875
- Cooley's anaemiaC0002875
- Cooley's anemiaC0002875
- Erythroblastic AnemiaC0002875
- Erythroblastic anemiaC0002875
- Homozygous beta thalassaemiaC0002875
- Homozygous beta thalassemiaC0002875
- Homozygous beta thalassemia (disorder)C0002875
- Homozygous thalassaemiaC0002875
- Homozygous thalassemiaC0002875
- Major, Thalassemia (beta-Thalassemia Major)C0002875
- Majors, Thalassemia (beta-Thalassemia Major)C0002875
- Mediterranean AnemiaC0002875
- Mediterranean AnemiasC0002875
- Mediterranean anaemiaC0002875
- Mediterranean anemiaC0002875
- Thalassaemia majorC0002875
- Thalassemia MajorC0002875
- Thalassemia Major (beta Thalassemia Major)C0002875
- Thalassemia Major (beta-Thalassemia Major)C0002875
- Thalassemia Majors (beta-Thalassemia Major)C0002875
- Thalassemia majorC0002875
- Thalassemia major (disorder)C0002875
- anemia cooley'sC0002875
- beta thalassaemia majorC0002875
- beta thalassemia majorC0002875
- cooley anemiaC0002875
- cooley's anaemiaC0002875
- cooley's anemiaC0002875
- cooleys anemiaC0002875
- homozygous beta thalassemiaC0002875
- major thalassemiaC0002875
- mediterranean anaemiaC0002875
- mediterranean anemiaC0002875
- thalassaemia majorC0002875
- thalassemia majorC0002875
- BETA-THALASSEMIAC0005283
- Beta ThalassemiaC0005283
- Beta thalassaemiaC0005283
- Beta thalassaemia syndromeC0005283
- Beta thalassemiaC0005283
- Beta thalassemia (disorder)C0005283
- Beta thalassemia syndromeC0005283
- Beta-thalassaemiaC0005283
- Microcytemia, beta TypeC0005283
- Microcytemias, beta TypeC0005283
- Thalassaemia betaC0005283
- Thalassemia betaC0005283
- Thalassemia, betaC0005283
- Thalassemia, beta TypeC0005283
- Thalassemia, beta typeC0005283
- Thalassemias, betaC0005283
- Thalassemias, beta TypeC0005283
- Type Microcytemia, betaC0005283
- Type Microcytemias, betaC0005283
- Type Thalassemia, betaC0005283
- Type Thalassemias, betaC0005283
- beta ThalassemiaC0005283
- beta ThalassemiasC0005283
- beta Type MicrocytemiaC0005283
- beta Type MicrocytemiasC0005283
- beta Type ThalassemiaC0005283
- beta Type ThalassemiasC0005283
- beta thalassaemiaC0005283
- beta thalassemiaC0005283
- beta thalassemiasC0005283
- beta-ThalassemiaC0005283
- beta-thalassaemiaC0005283
- beta-thalassemiaC0005283
- thalassaemia betaC0005283
- thalassemia betaC0005283
- Intermedia, ThalassemiaC0271979
- Intermedias, ThalassemiaC0271979
- THALASSEMIA INTERMEDIAC0271979
- Thalassaemia intermediaC0271979
- Thalassemia IntermediaC0271979
- Thalassemia IntermediasC0271979
- Thalassemia intermediaC0271979
- Thalassemia intermedia (disorder)C0271979
- thalassaemia intermediaC0271979
- thalassemia intermediaC0271979
- Severe beta thalassemiaC2873756
Frequently Asked Questions
What is ICD-10 code D56.1?
ICD-10-CM code D56.1 represents "Beta thalassemia". It is a billable/specific code that can be used on a claim.
Is D56.1 a billable code?
Yes, D56.1 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is D56.1 in?
D56.1 is in Chapter 3: Diseases of the Blood and Blood-Forming Organs (codes D50-D89).
What codes cannot be used with D56.1?
D56.1 has Excludes1 notes indicating codes that cannot be used together with it, including: sickle-cell thalassemia (D57.4-); beta thalassemia minor (D56.3); beta thalassemia trait (D56.3); and 3 more.
What SNOMED CT codes does D56.1 map to?
D56.1 maps to 21 SNOMED CT concepts: 5967006, 86715000, 27080008, 111572002, 79592006, and 16 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for D56.1?
D56.1 is linked to 4 UMLS Concept Unique Identifiers: C0002875, C0005283, C0271979, C2873756. 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.