Skip to content

Hemoglobin M Disease Screening (Mass Fraction of Hemoglobin in Red Blood Cells)

Published: August 9, 2026Updated: August 16, 2026

This test helps detect abnormal hemoglobin variants, which can cause red blood cells to break down prematurely and lead to anemia or other blood disorders.

Quick summary

["Screening for rare hemoglobin disorders that may affect red blood cell health and function."]

Medically reviewed by WellAlly Editorial TeamLast reviewed August 16, 2026Editorial policy

Key facts at a glance

LOINC
51614-6
Short code
Hgb M MFr Bld
Synonyms
Hgb M MFr Bld
Category
hematology
Sample
whole-blood
Container
Lavender-top (EDTA)
Units
N/A
Ref low
12
Ref high
17.5
Critical range
7 N/A – 20 N/A
Fasting
false
Population
adult
Sex
all
Age range
18–65 years
CPT
85018
SNOMED
900000000000003004
Specimen volume
3 mL
Stability
Room temperature: 4h, Refrigerated: 24h
Hemolysis max
0
Lipemia max
0
Icterus max
0
TAT
4–24 hours
Order
routine

What Is Hemoglobin M Disease?

Hemoglobin M disease is a genetic condition where your red blood cells produce an abnormal form of hemoglobin (the protein that carries oxygen). This variant can cause the cells to break down too soon, leading to anemia or other complications. The test measures the mass fraction of this abnormal hemoglobin in your blood.

Why Might You Need This Test?

Your healthcare provider may recommend this screening if you have symptoms like fatigue, weakness, or unusual pale skin, or if you have a family history of hemoglobin disorders. It’s also used as part of genetic testing for inherited blood conditions.

How Is the Test Performed?

A small blood sample is drawn from a vein in your arm. The test analyzes the hemoglobin composition in your red blood cells using mass fraction measurement techniques.

What Do the Results Mean?

Results may indicate the presence of abnormal hemoglobin variants. If elevated or abnormal levels are found, further genetic testing may be needed to confirm the diagnosis and guide treatment.

Reference range

Adult males: 13.5-17.5 g/dL; Females: 12.0-16.0 g/dLN/A

Specimen: whole-blood

No special preparation usually required. Stay well hydrated. Inform your healthcare provider of all medications and supplements you are taking.

Clinical interpretation

How abnormal results are interpreted and what conditions they suggest.

◆Associated findings1

Short name

Hemoglobin M Screening

Frequently asked questions

What are the normal results for this test?
Normal results would show typical hemoglobin composition without significant abnormal fractions. Abnormal results may require follow-up testing to identify specific variants.
Can this test be done at home?
No, this test requires a blood sample collected by a healthcare professional in a clinical setting.
How often should I get this test?
Your doctor will determine the frequency based on your symptoms, medical history, and risk factors. Regular monitoring may be recommended if you have a family history of hemoglobin disorders.
  1. 1
  2. 2
  3. 3

Click any link to access the full source. PubMed Central (PMC) links provide free full-text access.

This information is for educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment.

Medical Disclaimer

This content is for general informational and educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment. Always seek the guidance of a qualified healthcare provider with any questions you have about a medical condition, and never disregard professional medical advice or delay seeking it because of something you read here.

If you think you may have a medical emergency, call your local emergency number or go to the nearest emergency department immediately.

Medically reviewed by WellAlly Editorial Team Last reviewed August 16, 2026. · Read our editorial policy