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414393003: Hereditary disorder of cellular element of blood (disorder)

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

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 SNOMED CT core module
2534319013 Hereditary disorder of cellular element of blood en Synonym Active Entire term case insensitive SNOMED CT core module

297 descendants. Search Descendants:

Expanded Value Set

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

This concept is not in any reference sets

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