Z01.83
BillableEncounter for blood typing
Encounter for blood typing
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Encounter for Rh typing
Includes
Conditions included under this code
- routine examination of specific system
Excludes 1
Codes that cannot be used together with this code (mutual exclusion)
- examinations related to pregnancy and reproduction (Z30-Z36, Z39.-)
- encounter for examination for administrative purposes (Z02.-)
- encounter for examination for suspected conditions, proven not to exist (Z03.-)
- encounter for laboratory and radiologic examinations as a component of general medical examinations (Z00.0-)
- encounter for laboratory, radiologic and imaging examinations for sign(s) and symptom(s) - code to the sign(s) or symptom(s)
Excludes 2
Conditions not included here, but the patient may have both
- screening examinations (Z11-Z13)
Also Known As / Clinical Terms
SNOMED CT
- Blood group antigen C^u^3067005
- Weak C phenotype3067005
- Blood group antigen E^u^6800004
- Weak E phenotype6800004
- Blood group antigen G^u^16345006
- Weak G phenotype16345006
- Blood group p24403008
- P antigen type24403008
- P-null phenotype24403008
- p phenotype24403008
- Blood group N>2<25132006
- Weak N phenotype25132006
- Blood group S>2<25384006
- Weak S phenotype25384006
- Blood group antigen e^i^38194003
- Weak e phenotype38194003
- Blood group antigen V^u^57652005
- Weak V phenotype57652005
- Blood group O58460004
- Secretor gene absent (se)64553001
- Blood group M>2<65087006
- Weak M phenotype65087006
- Secretor gene present (Se)74836001
- Blood group antigen c^v^81835007
- Weak c phenotype81835007
- Blood group antigen D^u^89109006
- Rh negative Du positive89109006
- Weak D phenotype89109006
- Blood group P>2<103225004
- P>2< phenotype103225004
- Blood group B112149005
- Group B - blood112149005
- Lewis blood group phenotype115748000
- Le(a-b-) phenotype115749008
- Lewis null phenotype115749008
- I blood group phenotype115750008
- i>cord< phenotype115751007
- i>adult< phenotype115752000
- i>1< phenotype115753005
- i>2< phenotype115754004
- I phenotype115755003
- I>int< phenotype115756002
- Trans weak D phenotype115763002
- Inherited weak D phenotype115764008
- P blood group phenotype115794002
- P>1< phenotype115795001
- P>1<^k^ phenotype115796000
- P>2<^k^ phenotype115797009
- Landsteiner-Wiener phenotype115798004
- LW(a-b-) phenotype115799007
- Landsteiner-Wiener null phenotype115799007
- MNS null phenotype115801005
- M^k^M^k^ phenotype115801005
- U- phenotype115802003
- En(a-) phenotype115803008
- En(a-)(Fin) phenotype115804002
- En(a-)(UK) phenotype115805001
- En(a-)(United Kingdom) phenotype115805001
- Lu(a-b-) phenotype115822004
- Lutheran negative phenotype115822004
- LuLu phenotype115823009
- Recessive Lu(a-b-) phenotype115823009
- Dominant Lu(a-b-) phenotype115824003
- In(Lu) phenotype115824003
- XS2 phenotype115825002
- sex linked Lu(a-b-) phenotype115825002
- Acquired Lu(a-b-) phenotype115826001
- Acquired Lutheran negative phenotype115826001
- Lu(w) phenotype115827005
- Lutheran weak phenotype115827005
- Kidd blood group phenotype115830003
- Jk(a-b-) phenotype115831004
- JkJk phenotype115832006
- Recessive Jk(a-b-) phenotype115832006
- Dominant Jk(a-b-) phenotype115833001
- In(Jk) phenotype115833001
- Kell blood group phenotype115837000
- K>0< phenotype115838005
- Kell>null< phenotype115838005
- Kell>mod< phenotype115839002
- Kx blood group phenotype115844009
- Kx null phenotype115845005
- McLeod phenotype115845005
- Blood group AB165743006
- Group AB165743006
- Rh negative165746003
- RhD negative165746003
- Rhesus negative165746003
- Blood group O Rh(D) negative278148006
- Group O neg278148006
- Blood group A Rh(D) negative278152006
- Group A neg278152006
- Blood group B Rh(D) negative278153001
- Group B neg278153001
- Blood group AB Rh(D) negative278154007
- Group AB neg278154007
- Common composite blood groups365640002
- Common composite blood groups - finding365640002
- Finding of common composite blood group365640002
- Jk(a+) phenotype405854004
- Jk(a+b+) phenotype405855003
- Jk(a+b-) phenotype405856002
- Jk(a-) phenotype405857006
- Jk(a-b+) phenotype405858001
- Jk(b+) phenotype405859009
- Jk(b-) phenotype405860004
- Le(a+b-) phenotype405861000
- Le(a-b+) phenotype405862007
- Le(a-) phenotype405863002
- Le(a+) phenotype405864008
- Le(b+) phenotype405865009
- Le(b-) phenotype405866005
- Lu(a-b+) phenotype405868006
- Lu(a+b+) phenotype405869003
- Lu(a+b-) phenotype405870002
- Lu(a-) phenotype405871003
- Lu(a+) phenotype405872005
- Lu(b+) phenotype405873000
- Lu(b-) phenotype405874006
- M+ phenotype405875007
- M- phenotype405876008
- Le(a+b+) phenotype405877004
- N+ phenotype405878009
- N- phenotype405879001
- M-N- phenotype405880003
- M+N- phenotype405881004
- M+N+ phenotype405882006
- M-N+ phenotype405883001
- S- phenotype405884007
- S+ phenotype405885008
- s- phenotype405886009
- s+ phenotype405887000
- S+s+ phenotype405888005
- S-s+ phenotype405889002
- S-s- phenotype405890006
- S+s- phenotype405891005
- K+ phenotype405892003
- K- phenotype405893008
- k- phenotype405894002
- k+ phenotype405895001
- K+k+ phenotype405896000
- K+k- phenotype405897009
- K-k- phenotype405898004
- K-k+ phenotype405899007
- P1+ phenotype405900002
- P1- phenotype405901003
- Rhc negative733119003
- Rhc positive733120009
- Mixed field RhD1351894008
Frequently Asked Questions
What is the ICD-10 code for encounter for blood typing?
The ICD-10-CM code for encounter for blood typing is Z01.83. The full clinical description is "Encounter for blood typing". Z01.83 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code Z01.83 mean?
ICD-10-CM code Z01.83 represents "Encounter for blood typing". It is classified under Chapter 22: Factors Influencing Health Status and Contact With Health Services and is a billable/specific code that can be used on a claim.
Is Z01.83 a billable code?
Yes, Z01.83 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is Z01.83 in?
Z01.83 is in Chapter 22: Factors Influencing Health Status and Contact With Health Services (codes Z00-Z99).
What codes cannot be used with Z01.83?
Z01.83 has Excludes1 notes indicating codes that cannot be used together with it, including: examinations related to pregnancy and reproduction (Z30-Z36, Z39.-); encounter for examination for administrative purposes (Z02.-); encounter for examination for suspected conditions, proven not to exist (Z03.-); and 2 more.
What SNOMED CT codes does Z01.83 map to?
Z01.83 maps to 110 SNOMED CT concepts: 278153001, 115826001, 278152006, 165743006, 278154007, and 105 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for Z01.83?
Z01.83 is linked to 2 UMLS Concept Unique Identifiers: C2910501, C1561709. 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.