D81.5
BillablePurine nucleoside phosphorylase [PNP] deficiency
Purine nucleoside phosphorylase [PNP] deficiency
Coding Notes
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
SNOMED CT
- Deficiency of inosine phosphorylase60743005
- Deficiency of purine-nucleoside phosphorylase60743005
- NP - Nucleoside phosphorylase deficiency60743005
- NP deficiency60743005
- Nucleoside phosphorylase deficiency60743005
- PNP - Purine nucleoside phosphorylase deficiency60743005
- PNP deficiency60743005
- Purine nucleoside phosphorylase deficiency60743005
- Purine-nucleoside phosphorylase deficiency60743005
UMLS
- Deficiency of inosine phosphorylaseC0268125
- Deficiency of purine-nucleoside phosphorylaseC0268125
- NP - Nucleoside phosphorylase deficiencyC0268125
- NP deficiencyC0268125
- NUCLEOSIDE PHOSPHORYLASE DEFICIENCYC0268125
- Nucleoside Phosphorylase DeficiencyC0268125
- Nucleoside phosphorylase deficiencyC0268125
- PNP - Purine nucleoside phosphorylase deficiencyC0268125
- PNP DeficiencyC0268125
- PNP deficiencyC0268125
- PNPDC0268125
- PURINE NUCLEOSIDE PHOSPHORYLASE DEFICIENCYC0268125
- Purine Nucleoside Phosphorylase DeficiencyC0268125
- Purine nucleoside phosphorylase [PNP] deficiencyC0268125
- Purine nucleoside phosphorylase deficiencyC0268125
- Purine-Nucleoside Phosphorylase DeficiencyC0268125
- Purine-nucleoside phosphorylase deficiencyC0268125
- Purine-nucleoside phosphorylase deficiency (disorder)C0268125
Frequently Asked Questions
What is ICD-10 code D81.5?
ICD-10-CM code D81.5 represents "Purine nucleoside phosphorylase [PNP] deficiency". It is a billable/specific code that can be used on a claim.
Is D81.5 a billable code?
Yes, D81.5 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is D81.5 in?
D81.5 is in Chapter 3: Diseases of the Blood and Blood-Forming Organs (codes D50-D89).
What codes cannot be used with D81.5?
D81.5 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 1 more.
What SNOMED CT codes does D81.5 map to?
D81.5 maps to 1 SNOMED CT concept: 60743005. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for D81.5?
D81.5 is linked to 1 UMLS Concept Unique Identifier: C0268125. 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.