D61.09
BillableOther constitutional aplastic anemia
Other constitutional aplastic anemia
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Pancytopenia with malformations
Excludes 2
Conditions not included here, but the patient may have both
- •autoimmune disease (systemic) NOSM35.9
- •certain conditions originating in the perinatal periodP00-P96
- •complications of pregnancy, childbirth and the puerperiumO9A)O00
- •congenital malformations, deformations and chromosomal abnormalitiesQ00-Q99
- •endocrine, nutritional and metabolic diseasesE00-E88
- •human immunodeficiency virus [HIV] diseaseB20
- •injury, poisoning and certain other consequences of external causesS00-T88
- •neoplasmsC00-D49
- •symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classifiedR00-R94
- •neutropeniaD70
Related Codes(3)
Also Known As / Clinical Terms(105)
SNOMED CT
- Complete deafness8531006
- Congenital aplastic anaemia28975000
- Congenital aplastic anemia28975000
- Constitutional aplastic anaemia28975000
- Constitutional aplastic anemia28975000
- Hypoplastic anaemia - familial28975000
- Hypoplastic anemia - familial28975000
- Fanconi anaemia30575002
- Fanconi anemia30575002
- Fanconi pancytopenia syndrome30575002
- Fanconi's anaemia30575002
- Fanconi's anemia30575002
- Fanconi's familial refractory anaemia30575002
- Fanconi's familial refractory anemia30575002
- Fanconi's hypoplastic anaemia30575002
- Fanconi's hypoplastic anemia30575002
- Pancytopenia-dysmelia syndrome30575002
- Estren-Dameshek anaemia46760003
- Estren-Dameshek anemia46760003
- Congenital deafness95828007
- Immuno-osseous dysplasia254067002
- Constitutional aplastic anaemia with malformation267524009
- Constitutional aplastic anemia with malformation267524009
- Pancytopenia with malformation267524009
- WT limb blood syndrome719019000
- Pancytopenia with developmental delay syndrome774071007
- Trilineage bone marrow failure with developmental delay syndrome774071007
- Autosomal dominant aplasia and myelodysplasia778006008
- Autosomal dominant aplastic anaemia and myelodysplasia778006008
- Autosomal dominant aplastic anemia and myelodysplasia778006008
- Hereditary isolated aplastic anaemia783255002
- Hereditary isolated aplastic anemia783255002
- Congenital progressive bone marrow failure, B-cell immunodeficiency, skeletal dysplasia syndrome1177173001
- MYSM1 (Myb like, SWIRM and MPN domains 1) deficiency1177173001
- MYSM1 deficiency1177173001
- Myelodysplastic neoplasm with low blasts1260268001
- Myelodysplastic syndrome with low blasts1260268001
- Refractory neutropenia1260268001
- Fanconi anaemia of complementation group C1285021005
- Fanconi anemia of complementation group C1285021005
- Fanconi pancytopenia type 31285021005
- Fanconi's anaemia type C1285021005
- Fanconi's anemia type C1285021005
- AMeD (aplastic anaemia, intellectual disability, dwarfism) syndrome1332385000
- AMeD (aplastic anemia, intellectual disability, dwarfism) syndrome1332385000
- AMeD syndrome1332385000
- Aplastic anaemia, intellectual disability, dwarfism syndrome1332385000
- Aplastic anemia, intellectual disability, dwarfism syndrome1332385000
UMLS
- Constitutional aplastic anaemia with malformationC0340959
- Constitutional aplastic anemia with malformationC0340959
- Constitutional aplastic anemia with malformation (disorder)C0340959
- Pancytopenia with malformationC0340959
- Pancytopenia with malformationsC0340959
- Other Constitutional Aplastic AnemiaC1719322
- Other constitutional aplastic anemiaC1719322
Clinical Terms
- Hereditary isolated aplastic anemia
- Autosomal dominant aplastic anemia and myelodysplasia
- Fanconi's hypoplastic anaemia
- Fanconi anemia
- Aplastic anemia, intellectual disability, dwarfism syndrome
- Constitutional aplastic anaemia with malformation
- Estren-Dameshek anemia
- Hereditary isolated aplastic anaemia
- Fanconi anaemia
- Hypoplastic anemia - familial
- Complete deafness
- Myelodysplastic syndrome with low blasts
- Aplastic anaemia, intellectual disability, dwarfism syndrome
- Pancytopenia with developmental delay syndrome
- Fanconi anemia of complementation group C
- Pancytopenia with malformations
- Fanconi's familial refractory anaemia
- WT limb blood syndrome
- Trilineage bone marrow failure with developmental delay syndrome
- Fanconi's anaemia
- AMeD (aplastic anemia, intellectual disability, dwarfism) syndrome
- Refractory neutropenia
- Constitutional aplastic anaemia
- Pancytopenia-dysmelia syndrome
- Autosomal dominant aplastic anaemia and myelodysplasia
- Fanconi pancytopenia syndrome
- Myelodysplastic neoplasm with low blasts
- Congenital progressive bone marrow failure, B-cell immunodeficiency, skeletal dysplasia syndrome
- Constitutional aplastic anemia with malformation
- Fanconi's anaemia type C
- Fanconi's anemia
- Congenital aplastic anaemia
- Fanconi pancytopenia type 3
- Autosomal dominant aplasia and myelodysplasia
- Hypoplastic anaemia - familial
- Fanconi anaemia of complementation group C
- MYSM1 deficiency
- Pancytopenia with malformation
- Constitutional aplastic anemia with malformation (disorder)
- AMeD syndrome
- Fanconi's familial refractory anemia
- Estren-Dameshek anaemia
- Congenital deafness
- Fanconi's anemia type C
- Congenital aplastic anemia
- Immuno-osseous dysplasia
- MYSM1 (Myb like, SWIRM and MPN domains 1) deficiency
- AMeD (aplastic anaemia, intellectual disability, dwarfism) syndrome
- Constitutional aplastic anemia
- Fanconi's hypoplastic anemia
Frequently Asked Questions
What is the ICD-10 code for other constitutional aplastic anemia?
The ICD-10-CM code for other constitutional aplastic anemia is D61.09. The full clinical description is "Other constitutional aplastic anemia". D61.09 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code D61.09 mean?
ICD-10-CM code D61.09 represents “Other constitutional aplastic anemia”. 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 D61.09 a billable code?
Yes, D61.09 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is D61.09 in?
D61.09 is in Chapter 3: Diseases of the Blood and Blood-Forming Organs (codes D50-D89).
What SNOMED CT codes does D61.09 map to?
D61.09 maps to 15 SNOMED CT concepts: 1332385000, 778006008, 8531006, 28975000, 95828007, and 10 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for D61.09?
D61.09 is linked to 2 UMLS Concept Unique Identifiers: C0340959, C1719322. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
How does D61.09 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like other constitutional aplastic anemia affect a person's functioning — body functions, activities, participation, and environmental factors. AutoICD provides ICF Core Sets for 12+ conditions and can map clinical text to ICF categories automatically. Browse the ICF directory to explore functioning codes.
What is the ICD-11 equivalent of D61.09?
There is no direct ICD-11 mapping available for D61.09 in the WHO crosswalk tables. This may mean the concept is classified differently in ICD-11. Use the ICD-10 to ICD-11 converter to search for related codes.
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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.