LOINC Home

{component}   LP432695-7

Laboratory   LP29693-6

Molecular pathology   LP7822-2

Genes   LP32747-5

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.

▸ Abnormal clonal sequences   LP437683-8

▸ Genetic disease DNA and RNA analysis   LP436408-1

▸ Hereditary Wilms tumor multigene analysis   LP435136-9

▸ Erythrocytosis multigene analysis   LP437807-3

▸ Erythrocytosis focused multigene analysis   LP437808-1

▸ EBV Lymphoproliferation multigene analysis   LP437811-5

▸ Dysregulation autoimmune multigene analysis   LP437823-0

▸ Dyserythropoietic anemia multigene analysis   LP437806-5

▸ Distal weakness multigene analysis   LP437803-2

▸ Hereditary spastic paraplegia multigene analysis   LP437802-4

▸ Hereditary sensory neuropathy multigene analysis   LP437801-6

▸ Hereditary Motor Neuropathy multigene analysis   LP437337-1

▸ Hereditary motor and sensory neuropathy multigene analysis   LP437800-8

▸ Hereditary emery dreifuss multigene analysis   LP437805-7

▸ Hereditary congenital myasthenic syndrome multigene analysis   LP437804-0

▸ HMEP-Hemiplegic migraine multigene analysis   LP437792-7

▸ Hyper igE syndrome multigene analysis   LP437822-2

▸ Histiocytic neoplasm multigene analysis   LP437332-2

▸ Plasma cell myeloma multigene analysis   LP437879-2

▸ T cell lymphoma multigene analysis   LP437880-0

▸ RBC membrane multigene analysis   LP437810-7

▸ DNA fragmentation index   LP441136-1

▸ Cystinuria multigene analysis   LP442254-1

▸ SDHA and SDHB and SDHC and SDHD targeted gene mutation analysis   LP441834-1

▸ Renal cell carcinoma multigene analysis   LP441802-8

▸ Renal cell carcinoma fibromyomatous stroma multigene analysis   LP441800-2

▸ POLE targeted gene mutation analysis   LP441833-3

▸ Ovarian, fallopian tube and peritoneal carcinoma multigene analysis   LP441804-4

▸ NTRK1 and NTRK2 and NTRK3 targeted gene mutation analysis   LP441830-9

▸ MYOD1 targeted gene mutation analysis   LP441799-6

▸ Multiple myeloma minimal residual disease analysis   LP437816-4

▸ Mutations   LP7824-8

▸ Nucleotide repeats   LP193279-9

▸ MYC and BCL2 rearrangements   LP434773-0

▸ Myeloid sarcoma analysis   LP435023-9

▸ T-Cell acute lymphoblastic leukemia   LP434699-7

▸ Viral Susceptibility multigene analysis   LP437825-5

▸ Autoimmune lymphoproliferative syndrome multigene analysis   LP437826-3

▸ Breast Cancer recurrence risk multigene analysis   LP437602-8

▸ B cell non hodgkin Lymphoma multigene analysis   LP437882-6

▸ Chronic and low grade B cell lymphoid neoplasm multigene analysis   LP437881-8


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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