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LOINC Part Code LP32747-5 : Genes

Properties

parent MOLPATH LP7822-2
child Clonal sequences.abnormal LP437683-8
child Genetic disease DNA & RNA analysis LP436408-1
child Hereditary Wilms tumor multigene analysis LP435136-9
child Erythrocytosis multigene analysis LP437807-3
child Erythrocytosis focused multigene analysis LP437808-1
child EBV Lymphoproliferation multigene analysis LP437811-5
child Dysregulation autoimmune multigene analysis LP437823-0
child Dyserythropoietic anemia multigene analysis LP437806-5
child Distal weakness multigene analysis LP437803-2
child Hereditary spastic paraplegia multigene analysis LP437802-4
child Hereditary sensory neuropathy multigene analysis LP437801-6
child Hereditary Motor Neuropathy multigene analysis LP437337-1
child Hereditary motor and sensory neuropathy multigene analysis LP437800-8
child Hereditary emery dreifuss multigene analysis LP437805-7
child Hereditary congenital myasthenic syndrome multigene analysis LP437804-0
child Hemiplegic migraine multigene analysis LP437792-7
child Hyper igE syndrome multigene analysis LP437822-2
child Histiocytic neoplasm multigene analysis LP437332-2
child Plasma cell myeloma multigene analysis LP437879-2
child T cell lymphoma multigene analysis LP437880-0
child RBC membrane multigene analysis LP437810-7
child MOLPATH.MUT LP7824-8
child MOLPATH.NUCREPEAT LP193279-9
child MYC and BCL2 rearrangements LP434773-0
child Myeloid sarcoma analysis LP435023-9
child T-Cell acute lymphoblastic leukemia LP434699-7
child Viral Susceptibility multigene analysis LP437825-5
child Autoimmune lymphoproliferative syndrome multigene analysis LP437826-3
child Breast Cancer recurrence risk multigene analysis LP437602-8
child B cell non hodgkin Lymphoma multigene analysis LP437882-6
child Chronic and low grade B cell lymphoid neoplasm multigene analysis LP437881-8

Displays

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