LOINC Home

{component}   LP432695-7

Laboratory   LP29693-6

Molecular pathology   LP7822-2

Multigene studies   LP427513-9

LOINC Hierarchy


Select the title to see children of the section (▸) or the LOINC code. Select a code to view information about the section/code.

▸ Atypical hemolytic uremic syndrome multigene analysis   LP431375-7

▸ B-cell primary immunodeficiency multigene analysis   LP422654-6

▸ Cancer related large scale gene   LP172585-4

▸ Coronary heart disease multigene analysis   LP410958-5

▸ Ehlers-Danlos syndrome multigene analysis   LP410970-0

▸ Hearing loss multigene analysis   LP431382-3

▸ Hemophagocytic lymphohistiocytosis multigene analysis   LP431380-7

▸ Hereditary breast and gynecologic cancer multigene analysis   LP426460-4

▸ Hereditary cancer multigene analysis   LP426461-2

▸ Hereditary thrombocytopenia multigene analysis   LP431379-9

▸ Jewish descent preconception AndOr prenatal carrier screening multigene analysis   LP426474-5

▸ Myeloproliferative neoplasm multigene analysis   LP431087-8

▸ Preconception AndOr prenatal carrier screening multigene analysis   LP426473-7

▸ Preimplantation multigene analysis   LP434475-2

▸ Primary hyperoxaluria multigene analysis   LP412148-1

▸ Thrombotic microangiopathy multigene analysis   LP431376-5


Copyright © 2024 Regenstrief Institute, Inc. All Rights Reserved. To the extent included herein, the LOINC table and LOINC codes are copyright © 1995-2024, Regenstrief Institute, Inc. and the Logical Observation Identifiers Names and Codes (LOINC) Committee. See https://loinc.org/license for the full LOINC copyright and license.

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