MOLPATH LP7822-2

LOINC Hierarchy

LOINC part code	LP7822-2
name	MOLPATH
type	CLASS
status	ACTIVE
children	LOINC Home {component} LP432695-7 Laboratory LP29693-6 Molecular pathology LP7822-2 ▸ Genetics results LP70194-3 ▸ Mitochondria whole genome analysis LP433528-9 ▸ Genes LP32747-5 ▸ Ploidy LP32748-3 ▸ Multigene studies LP427513-9 ▸ Chromosome LP32750-9 ▸ Genetic screen LP19405-7 ▸ Microsatellite instability LP36464-3 ▸ Karyotype LP28493-2 ▸ Maternal cell contamination LP33231-9 ▸ GenBank sequence accession number LP262418-9 ▸ X linked heterotaxy LP62894-8 ▸ Cancer risk assessment LP192128-9 ▸ Identity testing LP76336-4 ▸ Heart transplant acute cellular rejection risk LP200197-4 ▸ Kidney transplant acute cellular rejection risk LP433666-7 ▸ Platelet disorders multigene analysis LP433075-1 ▸ Zygosity LP94227-3 ▸ Prostate cancer multigene analysis LP432157-8 ▸ Plasma cell proliferation analysis LP426512-2 ▸ SMN1 gene silent carrier analysis LP432502-5 ▸ Tripartite motif containing 46 LP437480-9 ▸ Noninvasive colorectal cancer RNA and occult blood screening LP441376-3 ▸ Noninvasive prenatal testing comment LP428617-7 ▸ VWF and GP1BA gene mutation analysis LP441715-2 ▸ Urea cycle disorders multigene analysis LP442261-6 ▸ Tyrosine disorders multigene analysis LP442260-8 ▸ Postmortem aortopathy multigene analysis LP441703-8 ▸ Porphyria multigene analysis LP441747-5 ▸ Phenylalanine disorders multigene analysis LP442259-0 ▸ Peroxisomal disorder multigene analysis LP442258-2 ▸ Offspring or Inheritance risk LP440976-1 ▸ Noonan syndrome and related conditions multigene analysis LP441829-1 ▸ Neuronal ceroid lipofuscinosis multigene analysis LP441746-7 ▸ Methylmalonate aciduria-propionic aciduria multigene analysis LP441744-2 ▸ Methylmalonate aciduria multigene analysis LP441742-6 ▸ Marfan and related conditions multigene analysis LP441828-3 ▸ Maple syrup urine disease multigene analysis LP441741-8 ▸ Lysosomal storage disease multigene analysis LP442257-4 ▸ Lung cancer screening LP440916-7 ▸ Ketone disorders multigene analysis LP442256-6 ▸ High DNA stainability LP441135-3 ▸ Hereditary thrombosis disorders multigene analysis LP441714-5 ▸ Hereditary platelet storage pool deficiency multigene analysis LP441713-7 ▸ Hereditary platelet function defect multigene analysis LP441708-7 ▸ Hereditary platelet disorders multigene analysis LP441709-5 ▸ Hereditary nonpolyposis colorectal cancer multigene analysis LP441826-7 ▸ Hereditary multigene analysis LP442253-3 ▸ Hereditary erythrocytosis multigene analysis LP441750-9 ▸ Hereditary bleeding disorders multigene analysis LP441705-3 ▸ Hereditary bleeding disorders factor and von Willebrand multigene analysis LP441706-1 ▸ Pharmacogenomics LP202929-8 ▸ Copy number variation analysis LP433611-3 ▸ Molecular Pathology Panels LP62072-1

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.

Thank you for choosing Find-A-Code, please Sign In to remove ads.

MY NEWSLETTERS

FEES

FACILITY

RISK ADJUSTMENT

LOINC Home

{component} LP432695-7

Laboratory LP29693-6

MOLPATH LP7822-2

LOINC Hierarchy

▸ Genetics results LP70194-3

▸ Mitochondria whole genome analysis LP433528-9

▸ Genes LP32747-5

▸ Ploidy LP32748-3

▸ Multigene studies LP427513-9

▸ Chromosome LP32750-9

▸ Genetic screen LP19405-7

▸ Microsatellite instability LP36464-3

▸ Karyotype LP28493-2

▸ Maternal cell contamination LP33231-9

▸ GenBank sequence accession number LP262418-9

▸ X linked heterotaxy LP62894-8

▸ Cancer risk assessment LP192128-9

▸ Identity testing LP76336-4

▸ Heart transplant acute cellular rejection risk LP200197-4

▸ Kidney transplant acute cellular rejection risk LP433666-7

▸ Platelet disorders multigene analysis LP433075-1

▸ Zygosity LP94227-3

▸ Prostate cancer multigene analysis LP432157-8

▸ Plasma cell proliferation analysis LP426512-2

▸ SMN1 gene silent carrier analysis LP432502-5

▸ Tripartite motif containing 46 LP437480-9

▸ Noninvasive colorectal cancer RNA and occult blood screening LP441376-3

▸ Noninvasive prenatal testing comment LP428617-7

▸ VWF and GP1BA gene mutation analysis LP441715-2

▸ Urea cycle disorders multigene analysis LP442261-6

▸ Tyrosine disorders multigene analysis LP442260-8

▸ Postmortem aortopathy multigene analysis LP441703-8

▸ Porphyria multigene analysis LP441747-5

▸ Phenylalanine disorders multigene analysis LP442259-0

▸ Peroxisomal disorder multigene analysis LP442258-2

▸ Offspring or Inheritance risk LP440976-1

▸ Noonan syndrome and related conditions multigene analysis LP441829-1

▸ Neuronal ceroid lipofuscinosis multigene analysis LP441746-7

▸ Methylmalonate aciduria-propionic aciduria multigene analysis LP441744-2

▸ Methylmalonate aciduria multigene analysis LP441742-6

▸ Marfan and related conditions multigene analysis LP441828-3

▸ Maple syrup urine disease multigene analysis LP441741-8

▸ Lysosomal storage disease multigene analysis LP442257-4

▸ Lung cancer screening LP440916-7

▸ Ketone disorders multigene analysis LP442256-6

▸ High DNA stainability LP441135-3

▸ Hereditary thrombosis disorders multigene analysis LP441714-5

▸ Hereditary platelet storage pool deficiency multigene analysis LP441713-7

▸ Hereditary platelet function defect multigene analysis LP441708-7

▸ Hereditary platelet disorders multigene analysis LP441709-5

▸ Hereditary nonpolyposis colorectal cancer multigene analysis LP441826-7

▸ Hereditary multigene analysis LP442253-3

▸ Hereditary erythrocytosis multigene analysis LP441750-9

▸ Hereditary bleeding disorders multigene analysis LP441705-3

▸ Hereditary bleeding disorders factor and von Willebrand multigene analysis LP441706-1

▸ Pharmacogenomics LP202929-8

▸ Copy number variation analysis LP433611-3

▸ Molecular Pathology Panels LP62072-1