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735452003: Hereditary vitamin B12 deficiency anemia (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2018. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3514569011 Hereditary vitamin B12 deficiency anemia (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3514570012 Hereditary vitamin B12 deficiency anemia en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3514571011 Hereditary vitamin B12 deficiency anaemia en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3514569011 Hereditary vitamin B12 deficiency anemia (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3514570012 Hereditary vitamin B12 deficiency anemia en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3514571011 Hereditary vitamin B12 deficiency anaemia en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
6306341000241118 anémie héréditaire par carence en vitamine B12 fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6306351000241115 anémie héréditaire par carence en cobalamine fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6306341000241118 anémie héréditaire par carence en vitamine B12 fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6306351000241115 anémie héréditaire par carence en cobalamine fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hereditary vitamin B12 deficiency anemia (disorder) Due to Cobalamin deficiency true Inferred relationship Existential restriction modifier (core metadata concept) 2
Hereditary vitamin B12 deficiency anemia (disorder) Is a Hereditary disease true Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary vitamin B12 deficiency anemia (disorder) Is a Megaloblastic anaemia due to vitamin B>12< deficiency true Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary vitamin B12 deficiency anemia (disorder) Has interpretation Below reference range true Inferred relationship Existential restriction modifier (core metadata concept) 3
Hereditary vitamin B12 deficiency anemia (disorder) Interprets Measurement of total haemoglobin concentration true Inferred relationship Existential restriction modifier (core metadata concept) 3
Hereditary vitamin B12 deficiency anemia (disorder) Has interpretation Below reference range false Inferred relationship Existential restriction modifier (core metadata concept) 4
Hereditary vitamin B12 deficiency anemia (disorder) Interprets Red blood cell count false Inferred relationship Existential restriction modifier (core metadata concept) 4
Hereditary vitamin B12 deficiency anemia (disorder) Is a Hemoglobin below reference range (finding) true Inferred relationship Existential restriction modifier (core metadata concept)
Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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