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360495000: Familial megaloblastic anemia (disorder)


Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
476330019 Familial megaloblastic anemia en Synonym Active Case insensitive SNOMED CT core
476331015 Familial megaloblastic anaemia en Synonym Active Case insensitive SNOMED CT core
740528011 Familial megaloblastic anemia (disorder) en Fully specified name Active Case insensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Familial megaloblastic anaemia Is a Megaloblastic anaemia due to inborn errors of metabolism true Inferred relationship Some
Familial megaloblastic anaemia Has definitional manifestation Erythropenia false Inferred relationship Some
Familial megaloblastic anaemia Finding site Haematopoietic system structure false Inferred relationship Some
Familial megaloblastic anaemia Has interpretation Below reference range true Inferred relationship Some 1
Familial megaloblastic anaemia Has interpretation Below reference range true Inferred relationship Some 2
Familial megaloblastic anaemia Interprets Red blood cell count true Inferred relationship Some 1
Familial megaloblastic anaemia Interprets Measurement of total haemoglobin concentration true Inferred relationship Some 2
Familial megaloblastic anaemia Finding site Erythrocyte false Inferred relationship Some
Familial megaloblastic anaemia Occurrence Congenital true Inferred relationship Some 3
Familial megaloblastic anaemia Finding site Haematopoietic system structure false Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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