711160007: Eosinophil peroxidase deficiency (disorder)

• SNOMED CT Concept\Clinical finding\...
• \Finding of blood, lymphatics and immune system\Blood disease\White blood cell disorder\Non-malignant white cell disorder\Eosinophil peroxidase deficiency
• \Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Eosinophil peroxidase deficiency
• \Disease\Disorder of immune function\White blood cell disorder\Non-malignant white cell disorder\Eosinophil peroxidase deficiency
• \Disease\Blood disease\White blood cell disorder\Non-malignant white cell disorder\Eosinophil peroxidase deficiency

Status: current, Primitive. Date: 31-Jul 2015. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3047543010	Eosinophil peroxidase deficiency (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core
3047544016	Eosinophil peroxidase deficiency	en	Synonym	Active	Case insensitive	SNOMED CT core
3047545015	Presentey anomaly	en	Synonym	Active	Case sensitive	SNOMED CT core
3047546019	Peroxidase and phospholipid deficiency in eosinophils	en	Synonym	Active	Case insensitive	SNOMED CT core

Expanded Value Set

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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