LOINC Code 85505-6: Presumptive Rh Molgen Nom (Sal)
85505-6 is a LOINC code used to identify Presumptive Rh Molgen Nom (Sal) in laboratory and clinical observation data. You may see this code in lab systems, lab reports, EHR exports, interoperability feeds, or other structured clinical data exchanges. LOINC codes identify tests, measurements, observations, survey items, and clinical questions in a standardized way. It is associated with the component Rh.presumptive. It is commonly used with the system or sample type Saliva.
What is this code?
LOINC codes identify tests, measurements, observations, survey items, and clinical questions in a standardized way. It is associated with the component Rh.presumptive. It is commonly used with the system or sample type Saliva.
When is it used?
- Used in lab systems, EHRs, and clinical data exchange.
- May identify a test, observation, survey item, or clinical document request rather than a diagnosis.
- Status: ACTIVE
- Order vs observation: Both
- Method: Molgen
What it does not mean
- The code identifies the observation or test, not the actual result.
Key facts
- Presumptive Rh [Type] in Saliva (oral fluid) by Molecular genetics method
- Rh.presumptive
- The presumptive (predicted) Rh factor for the D antigen (Rh positive or Rh negative) based on genetic analysis of the RHD gene. Hematopoietic stem cell transplant donor registries often collect samples from potential donors using buccal swabs or saliva (both described as "saliva" in the LOINC term) as part of enrolling them in the registry. Because these samples do not contain fresh intact red blood cells (RBCs) and traditional serological RhD blood group typing cannot be done, molecular typing is performed as part of the screening process to find an appropriate hematopoietic stem cell donor. Prior to transfusion or transplantation, the presumptive Rh factor result based on molecular typing must be confirmed using traditional serologic typing. This term was created for, but not limited in use to, the submitter's lab that performs sequence analysis of select exons in the RHD gene and predicts the RhD phenotype from the resulting DNA sequence.
- BLOOD BANK; D phenotyping; D typing; Molecular genetics; Nominal; Oral fluid; PCR; Point in time; Random; Rh phenotyping; Rh typing; Sal; Typ
Where you may see this code
You may see this code in lab systems, lab reports, EHR exports, interoperability feeds, or other structured clinical data exchanges.
Common synonyms
Frequently asked questions
About this content
This page is prepared by HealthAssure's clinical team using official coding standards from LOINC. AI tools assist with drafting explanations, which are then reviewed and verified by healthcare professionals for accuracy. This content is for informational purposes and does not replace professional medical advice. Meet our team.