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48983004: X chromosome-linked sideroblastic anemia (disorder)


Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2018. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
2716922011 X chromosome-linked sideroblastic anemia (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
3657179014 X-linked sideroblastic anemia en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3657180012 X-linked sideroblastic anaemia en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
495279012 X chromosome-linked sideroblastic anaemia en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
81603013 X chromosome-linked sideroblastic anemia en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3657181011 A constitutional microcytic, hypochromic anemia of varying severity that is clinically characterized by manifestations of anemia and iron overload and that may respond to treatment with pyridoxine and folic acid. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3657182016 A constitutional microcytic, hypochromic anaemia of varying severity that is clinically characterised by manifestations of anaemia and iron overload and that may respond to treatment with pyridoxine and folic acid. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core


3 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
X chromosome-linked sideroblastic anemia (disorder) est un(e) (attribut) X-linked recessive hereditary disease true Inferred relationship Some
X chromosome-linked sideroblastic anemia (disorder) est un(e) (attribut) Sideroblastic anemia true Inferred relationship Some
X chromosome-linked sideroblastic anemia (disorder) est un(e) (attribut) Inherited disorder of porphyrin metabolism (disorder) true Inferred relationship Some
X chromosome-linked sideroblastic anemia (disorder) interprète (attribut) Red blood cell count true Inferred relationship Some 2
X chromosome-linked sideroblastic anemia (disorder) est un(e) (attribut) X-linked hereditary disease false Inferred relationship Some
X chromosome-linked sideroblastic anemia (disorder) a pour interprétation (attribut) au-dessous de l'étendue de référence true Inferred relationship Some 2
X chromosome-linked sideroblastic anemia (disorder) interprète (attribut) Measurement of total haemoglobin concentration true Inferred relationship Some 1
X chromosome-linked sideroblastic anemia (disorder) survenue (attribut) congénital true Inferred relationship Some 3
X chromosome-linked sideroblastic anemia (disorder) a pour interprétation (attribut) au-dessous de l'étendue de référence true Inferred relationship Some 1
X chromosome-linked sideroblastic anemia (disorder) localisation d'une constatation (attribut) Erythrocyte true Inferred relationship Some 3
X chromosome-linked sideroblastic anemia (disorder) est un(e) (attribut) Hereditary red blood cell disorder (disorder) true Inferred relationship Some
X chromosome-linked sideroblastic anemia (disorder) est un(e) (attribut) Congenital anemia true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group
X chromosome-linked pyridoxine responsive sideroblastic anemia est un(e) (attribut) True X chromosome-linked sideroblastic anemia (disorder) Inferred relationship Some
X chromosome-linked pyridoxine refractory sideroblastic anemia est un(e) (attribut) True X chromosome-linked sideroblastic anemia (disorder) Inferred relationship Some
X-linked sideroblastic anemia with spinocerebellar ataxia est un(e) (attribut) True X chromosome-linked sideroblastic anemia (disorder) Inferred relationship Some

This concept is not in any reference sets

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