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 purposesZ02
- •encounter for examination for suspected conditions, proven not to existZ03
- •encounter for laboratory and radiologic examinations as a component of general medical examinationsZ00.0
- encounter for laboratory, radiologic and imaging examinations for sign(s) and symptom(s) - code to the sign(s) or symptom(s)
Related Codes(4)
Also Known As / Clinical Terms(295)
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
Clinical Terms
- Weak e phenotype
- Blood group O Rh(D) negative
- Jk(a-) phenotype
- K+k- phenotype
- LW(a-b-) phenotype
- P-null phenotype
- Rh negative
- Landsteiner-Wiener null phenotype
- Group O neg
- Blood group B
- Le(a-) phenotype
- P antigen type
- Le(a+b+) phenotype
- Weak M phenotype
- McLeod phenotype
- Le(a+b-) phenotype
- Rh negative Du positive
- Jk(a+) phenotype
- Blood group antigen C^u^
- JkJk phenotype
- Landsteiner-Wiener phenotype
- Dominant Jk(a-b-) phenotype
- Blood group antigen E^u^
- Lutheran negative phenotype
- Blood group N>2<
- Weak c phenotype
- Blood group antigen c^v^
- K>0< phenotype
- S+ phenotype
- Le(a-b+) phenotype
- Lu(b-) phenotype
- P1- phenotype
- K+k+ phenotype
- Kx null phenotype
- i>cord< phenotype
- Trans weak D phenotype
- Weak G phenotype
- Rhesus negative
- Blood group antigen e^i^
- Weak N phenotype
- Secretor gene present (Se)
- I>int< phenotype
- Jk(b-) phenotype
- Blood group A Rh(D) negative
- Jk(b+) phenotype
- P>1<^k^ phenotype
- Blood group AB Rh(D) negative
- M+N- phenotype
- Finding of common composite blood group
- Recessive Lu(a-b-) phenotype
- M+N+ phenotype
- Blood group S>2<
- Blood group AB
- Encounter for Rh typing
- P>1< phenotype
- Acquired Lu(a-b-) phenotype
- En(a-)(Fin) phenotype
- Rhc negative
- M^k^M^k^ phenotype
- Le(b-) phenotype
- Blood group p
- Group B neg
- Kidd blood group phenotype
- Jk(a+b-) phenotype
- In(Jk) phenotype
- U- phenotype
- K+ phenotype
- Le(a-b-) phenotype
- RhD negative
- M-N+ phenotype
- En(a-)(United Kingdom) phenotype
- Inherited weak D phenotype
- P1+ phenotype
- Blood group M>2<
- Lu(b+) phenotype
- P>2< phenotype
- sex linked Lu(a-b-) phenotype
- Mixed field RhD
- Jk(a-b-) phenotype
- En(a-)(UK) phenotype
- I blood group phenotype
- Dominant Lu(a-b-) phenotype
- LuLu phenotype
- In(Lu) phenotype
- Lu(w) phenotype
- S+s+ phenotype
- XS2 phenotype
- Blood group P>2<
- Secretor gene absent (se)
- K- phenotype
- P blood group phenotype
- Lewis null phenotype
- M+ phenotype
- MNS null phenotype
- Lu(a+) phenotype
- K-k+ phenotype
- Kell blood group phenotype
- Recessive Jk(a-b-) phenotype
- Group B - blood
- Jk(a+b+) phenotype
- Kell>null< phenotype
- Weak D phenotype
- Common composite blood groups
- Acquired Lutheran negative phenotype
- N+ phenotype
- I phenotype
- Lu(a+b-) phenotype
- M-N- phenotype
- N- phenotype
- S+s- phenotype
- Lu(a-b-) phenotype
- Common composite blood groups - finding
- Jk(a-b+) phenotype
- En(a-) phenotype
- Rhc positive
- i>adult< phenotype
- Group AB neg
- P>2<^k^ phenotype
- M- phenotype
- Weak V phenotype
- S-s- phenotype
- Blood group B Rh(D) negative
- Group AB
- p phenotype
- S- phenotype
- Kx blood group phenotype
- Lewis blood group phenotype
- S-s+ phenotype
- Kell>mod< phenotype
- Blood group antigen D^u^
- Group A neg
- Lu(a+b+) phenotype
- i>1< phenotype
- Blood group antigen V^u^
- K-k- phenotype
- Le(a+) phenotype
- i>2< phenotype
- Weak S phenotype
- Blood group antigen G^u^
- Lu(a-b+) phenotype
- Lutheran weak phenotype
- Le(b+) phenotype
- Blood group O
- Lu(a-) phenotype
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: 115826001, 278152006, 165743006, 278154007, 112149005, 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.
How does Z01.83 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like encounter for blood typing 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 Z01.83?
There is no direct ICD-11 mapping available for Z01.83 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.