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
▸ Severe congenital and cyclic neutropenia multigene analysis LP450933-9
▸ Epilepsy and seizure multigene analysis LP450934-7
Copyright © 2026 Regenstrief Institute, Inc. All Rights Reserved. To the extent included herein, the LOINC table and LOINC codes are copyright © 1995-2026, 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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