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735452003: Hereditary vitamin B12 deficiency anemia (disorder)


Status: current, Primitive. 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 Initial character case insensitive SNOMED CT core
3514570012 Hereditary vitamin B12 deficiency anemia en Synonym Active Initial character case insensitive SNOMED CT core
3514571011 Hereditary vitamin B12 deficiency anaemia en Synonym Active Initial character case insensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hereditary vitamin B12 deficiency anaemia Is a Haemoglobin low true Inferred relationship Some
Hereditary vitamin B12 deficiency anaemia Due to Vitamin B12 deficiency true Inferred relationship Some 2
Hereditary vitamin B12 deficiency anaemia Is a Hereditary disease true Inferred relationship Some
Hereditary vitamin B12 deficiency anaemia Is a Megaloblastic anaemia due to vitamin B>12< deficiency true Inferred relationship Some
Hereditary vitamin B12 deficiency anaemia Has interpretation Below reference range true Inferred relationship Some 3
Hereditary vitamin B12 deficiency anaemia Interprets Measurement of total haemoglobin concentration true Inferred relationship Some 3
Hereditary vitamin B12 deficiency anaemia Has interpretation Below reference range false Inferred relationship Some 4
Hereditary vitamin B12 deficiency anaemia Interprets Red blood cell count false Inferred relationship Some 4

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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