Biomarkers · Chemical
CAH 21-Hydroxylase Deficiency Common Mutations
- Also listed as
- total calcium, CAH (21-Hydroxylase Deficiency) Common Mutations, serum calcium, ca
- LOINC codes
- 30005-3
- Tests that measure CAH 21-Hydroxylase Deficiency Common Mutations
- Quest Diagnostics 1
Tests
Check the catalog code, specimen, method and preparation for every test that measures CAH 21-Hydroxylase Deficiency Common Mutations. Select up to five tests to compare them side by side.
Quest Diagnostics 1 test
Panels that include this biomarker
CAH (21-Hydroxylase Deficiency) Common Mutations 14755
2 analytes · Blood · Fasting not stated · Turnaround Set up: Mon; Report available: 7-14 days
Quest Diagnostics catalog pageMethod and collection
- Method
- Electrophoresis • Minisequencing • Polymerase Chain Reaction (PCR)
- Collection
- Store and ship at room temperature immediately. Do not freeze.
- Reference notes
- See Laboratory Report
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Quest Diagnostics test catalog
1 test: codes, specimens, methods, preparation and reference intervals.
LOINC 30005-3
Regenstrief Institute codes that identify the same result across labs.
Search ClinicalTrials.gov for CAH 21-Hydroxylase Deficiency Common Mutations
Registered studies that measure CAH 21-Hydroxylase Deficiency Common Mutations, on the U.S. National Library of Medicine registry.
Verify these ranges and sources
We compile this page from named laboratory catalogs, guidelines and studies. Labs calculate reference intervals from the people they test, for one assay method and one population group, so an interval describes that population rather than an optimal target.
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