D58.1
BillableHereditary elliptocytosis
Hereditary elliptocytosis
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Elliptocytosis (congenital)
- Ovalocytosis (congenital) (hereditary)
Excludes 1
Codes that cannot be used together with this code (mutual exclusion)
- hemolytic anemia of the newborn (P55.-)
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
- Stomatocytosis3272007
- Hereditary elliptocytosis due to deficiency of protein 4.15994005
- Hereditary elliptocytosis due to alpha spectrin defect8857001
- Hereditary elliptocytosis due to glycophorin C deficiency15121005
- Hereditary elliptocytosis due to beta spectrin-ankyrin interaction66262001
- Hereditary elliptocytosis due to beta spectrin defect in self-association73073009
- Hereditary elliptocytosis due to abnormal protein 4.175443009
- Congenital elliptocytosis191169008
- HE - hereditary elliptocytosis191169008
- Hereditary elliptocytosis191169008
- Hereditary ovalocytosis191169008
- Hereditary elliptocytosis with transient poikilocytosis234410008
- Elliptocytosis250242004
- Ovalocytosis250242004
- Congenital nephritis276585000
- AMME complex720982007
- AMME syndrome720982007
- Alport syndrome, intellectual disability, midface hypoplasia, elliptocytosis syndrome720982007
- Melanesian ovalocytosis723623002
- Southeast Asian ovalocytosis723623002
- Stomatocytic elliptocytosis723623002
- Homozygous hereditary elliptocytosis1153399000
UMLS
- Congenital elliptocytosisC0013902
- Elliptocytoses, HereditaryC0013902
- ElliptocytosisC0013902
- Elliptocytosis (congenital)C0013902
- Elliptocytosis hereditaryC0013902
- Elliptocytosis, HereditaryC0013902
- HE - hereditary elliptocytosisC0013902
- Hereditary ElliptocytosesC0013902
- Hereditary ElliptocytosisC0013902
- Hereditary OvalocytosesC0013902
- Hereditary OvalocytosisC0013902
- Hereditary elliptocytosisC0013902
- Hereditary elliptocytosis (disorder)C0013902
- Hereditary ovalocytosisC0013902
- Ovalocytoses, HereditaryC0013902
- Ovalocytosis (congenital) (hereditary)C0013902
- Ovalocytosis, HereditaryC0013902
- elliptocytosisC0013902
- elliptocytosis hereditaryC0013902
- hereditary elliptocytosisC0013902
- hereditary ovalocytosisC0013902
- ovalocytosisC0013902
Frequently Asked Questions
What is ICD-10 code D58.1?
ICD-10-CM code D58.1 represents "Hereditary elliptocytosis". It is a billable/specific code that can be used on a claim.
Is D58.1 a billable code?
Yes, D58.1 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is D58.1 in?
D58.1 is in Chapter 3: Diseases of the Blood and Blood-Forming Organs (codes D50-D89).
What codes cannot be used with D58.1?
D58.1 has Excludes1 notes indicating codes that cannot be used together with it, including: hemolytic anemia of the newborn (P55.-).
What SNOMED CT codes does D58.1 map to?
D58.1 maps to 14 SNOMED CT concepts: 720982007, 191169008, 276585000, 250242004, 75443009, and 9 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for D58.1?
D58.1 is linked to 1 UMLS Concept Unique Identifier: C0013902. 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.