Sign in →

Test Code MAMH Antimullerian Hormone (AMH), Serum

Additional Codes

 

MAYO Test ID

AMH

EPIC Test ID

LAB1733

 

Reporting Name

Antimullerian Hormone, S

Useful For

Assessment of menopausal status, including premature ovarian failure

 

Assessing ovarian status, including ovarian reserve and ovarian responsiveness, as part of an evaluation for infertility and assisted reproduction protocols such as in vitro fertilization

 

Assessing ovarian function in patients with polycystic ovarian syndrome

 

Evaluation of infants with ambiguous genitalia and other intersex conditions

 

Evaluating testicular function in infants and children

 

Monitoring patients with antimullerian hormone-secreting ovarian granulosa cell tumors

Method Name

Enzyme-Linked Immunosorbent Assay (ELISA)

Performing Laboratory

Mayo Medical Laboratories in Rochester

Specimen Type

Serum


Specimen Required


Collection Container/Tube:

Preferred: Red top

Acceptable: Serum gel

Submission Container/Tube: Plastic screw-top aliquot tube

Specimen Volume: 0.5 mL


Specimen Minimum Volume

0.1 mL

Specimen Stability Information

Specimen Type Temperature Time
Serum Refrigerated (preferred) 7 days
  Frozen  90 days

Reject Due To

Hemolysis

Mild OK; Gross reject acceptable to 2,000 mg/dL

Lipemia

Mild OK, Gross OK

Icterus

NA

Other

NA

 

Reference Values

Males

<24 months: 14-466 ng/mL

24 months-12 years: 7.4-243 ng/mL

>12 years: 0.7-19 ng/mL

Females

<24 months: <4.7 ng/mL

24 months-12 years: <8.8 ng/mL

13-45 years: 0.9-9.5 ng/mL

>45 years: <1.0 ng/mL

Day(s) and Time(s) Performed

Monday through Friday; 6 a.m.-5 p.m.

CPT Code Information

83520

LOINC Code Information

Test ID Test Order Name Order LOINC Value
AMH Antimullerian Hormone, S 83104-0

 

Result ID Test Result Name Result LOINC Value
89711 Antimullerian Hormone, S 83104-0

Analytic Time

1 day

Test Classification

This test was developed and its performance characteristics determined by Mayo Clinic in a manner consistent with CLIA requirements. This test has not been cleared or approved by the U.S. Food and Drug Administration.

Forms

If not ordering electronically, complete, print, and send a General Request Form (T239) with the specimen (http://www.mayomedicallaboratories.com/it-mmfiles/general-request-form.pdf).