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414393003: hereditaire aandoening van cellulair component van bloed (aandoening)

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2005. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
2530854017 Hereditary disorder of cellular element of blood (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
2534319013 Hereditary disorder of cellular element of blood en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
6701451000146116 erfelijke ziekte van cel in bloed nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
6702491000146118 hereditaire aandoening van cellulair component van bloed (aandoening) nl Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
6702501000146111 hereditaire aandoening van cellulair component van bloed nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)

315 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hereditary disorder of cellular element of blood (disorder) Is a Hereditary disorder by system true Inferred relationship Some
Hereditary disorder of cellular element of blood (disorder) Is a Disorder of cellular component of blood (disorder) true Inferred relationship Some
Hereditary disorder of cellular element of blood (disorder) Has definitional manifestation Finding of cellular component of blood (finding) false Inferred relationship Some
Hereditary disorder of cellular element of blood (disorder) Finding site Body system structure true Inferred relationship Some 1
Inbound Relationships Type Active Source Characteristic Refinability Group
Hereditary red blood cell disorder (disorder) Is a True Hereditary disorder of cellular element of blood (disorder) Inferred relationship Some
Hereditary white blood cell disorder (disorder) Is a True Hereditary disorder of cellular element of blood (disorder) Inferred relationship Some
Inherited platelet disorder Is a False Hereditary disorder of cellular element of blood (disorder) Inferred relationship Some
Hermansky-Pudlak syndrome Is a False Hereditary disorder of cellular element of blood (disorder) Inferred relationship Some
Radial aplasia-thrombocytopenia syndrome Is a False Hereditary disorder of cellular element of blood (disorder) Inferred relationship Some
macrotrombocytopenie met doofheid en nefropathie (aandoening) Is a False Hereditary disorder of cellular element of blood (disorder) Inferred relationship Some
Wiskott-Aldrich syndrome Is a False Hereditary disorder of cellular element of blood (disorder) Inferred relationship Some
Inherited platelet disorder Is a True Hereditary disorder of cellular element of blood (disorder) Inferred relationship Some
WT limb blood syndrome (disorder) Is a False Hereditary disorder of cellular element of blood (disorder) Inferred relationship Some
Revesz syndrome (disorder) Is a False Hereditary disorder of cellular element of blood (disorder) Inferred relationship Some
Megaloblastic anemia, thiamine-responsive, with diabetes mellitus and sensorineural deafness Is a True Hereditary disorder of cellular element of blood (disorder) Inferred relationship Some
Mitochondrial myopathy with sideroblastic anemia syndrome (disorder) Is a True Hereditary disorder of cellular element of blood (disorder) Inferred relationship Some
Congenital sideroblastic anemia, B-cell immunodeficiency, periodic fever, developmental delay syndrome Is a True Hereditary disorder of cellular element of blood (disorder) Inferred relationship Some
Aase syndrome Is a True Hereditary disorder of cellular element of blood (disorder) Inferred relationship Some
Ghosal hematodiaphyseal dysplasia Is a True Hereditary disorder of cellular element of blood (disorder) Inferred relationship Some
Carbamoyl-phosphate synthetase 2, aspartate transcarbamylase, and dihydroorotase congenital disorder of glycosylation (disorder) Is a True Hereditary disorder of cellular element of blood (disorder) Inferred relationship Some

Reference Sets

Description inactivation indicator reference set

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