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259358008: Amino acid metabolism disorder marker (substance)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
386250013 Amino acid metabolism disorder marker en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
650906013 Amino acid metabolism disorder marker (substance) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
386250013 Amino acid metabolism disorder marker en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
386250013 Amino acid metabolism disorder marker en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
650906013 Amino acid metabolism disorder marker (substance) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
650906013 Amino acid metabolism disorder marker (substance) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core


49 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Amino acid metabolism disorder marker Is a Inborn errors of metabolism marker (substance) true Inferred relationship Existential restriction modifier (core metadata concept)

Inbound Relationships Type Active Source Characteristic Refinability Group
Phenylalanine and tyrosine disorder marker (substance) Is a True Amino acid metabolism disorder marker Inferred relationship Existential restriction modifier (core metadata concept)
Urea cycle disorder marker (substance) Is a True Amino acid metabolism disorder marker Inferred relationship Existential restriction modifier (core metadata concept)
Ornithine and lysine metabolism disorder marker Is a True Amino acid metabolism disorder marker Inferred relationship Existential restriction modifier (core metadata concept)
Sulphur amino acid disorder markers Is a True Amino acid metabolism disorder marker Inferred relationship Existential restriction modifier (core metadata concept)
N-Acetylaspartate Is a False Amino acid metabolism disorder marker Inferred relationship Existential restriction modifier (core metadata concept)
Proline-rich iminodipeptides Is a True Amino acid metabolism disorder marker Inferred relationship Existential restriction modifier (core metadata concept)
L-Histidine Is a False Amino acid metabolism disorder marker Inferred relationship Existential restriction modifier (core metadata concept)
Glycine Is a True Amino acid metabolism disorder marker Inferred relationship Existential restriction modifier (core metadata concept)
Histidine ammonia-lyase (substance) Is a True Amino acid metabolism disorder marker Inferred relationship Existential restriction modifier (core metadata concept)
Xaa-Pro dipeptidase Is a True Amino acid metabolism disorder marker Inferred relationship Existential restriction modifier (core metadata concept)
Aspartoacylase Is a True Amino acid metabolism disorder marker Inferred relationship Existential restriction modifier (core metadata concept)
Amino acids 6% solution The clinically relevant part or whole of the substance that is intended to have a therapeutic action on or within the body. It excludes esters, salts or other non-covalent derivatives (such as a complex, chelate etc.), but may include secondary modifications. False Amino acid metabolism disorder marker Inferred relationship Existential restriction modifier (core metadata concept)
Cytosol non-specific dipeptidase Is a True Amino acid metabolism disorder marker Inferred relationship Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

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