366961000119106: Albinism co-occurrent with hematologic disorder (disorder)

• SNOMED CT Concept\Clinical finding\Disease\...
• \Genetic disease\Hereditary disease\...
• \Hereditary metabolic disease\Inborn error of metabolism\Albinism\Albinism co-occurrent with haematologic disorder
• \Hereditary disorder by system\Albinism co-occurrent with haematologic disorder
• \Developmental hereditary disorder\Albinism\Albinism co-occurrent with haematologic disorder
• \Disorder of pigmentation\Albinism\Albinism co-occurrent with haematologic disorder
• \Disorder of body system\Disorder of haematopoietic structure\Albinism co-occurrent with haematologic disorder
• \Disorder of body system\Hereditary disorder by system\Albinism co-occurrent with haematologic disorder
• \Metabolic disease\Hereditary metabolic disease\Inborn error of metabolism\Albinism\Albinism co-occurrent with haematologic disorder
• \Congenital disease\Congenital anomaly\Albinism\Albinism co-occurrent with haematologic disorder
• \Congenital disease\Inborn error of metabolism\Albinism\Albinism co-occurrent with haematologic disorder
• \Developmental disorder\Developmental hereditary disorder\Albinism\Albinism co-occurrent with haematologic disorder
• \Developmental disorder\Congenital anomaly\Albinism\Albinism co-occurrent with haematologic disorder

Status: current, Defined. Date: 31-Jan 2016. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3289782017	Albinism co-occurrent with hematologic disorder (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core
3289788018	Albinism co-occurrent with hematologic disorder	en	Synonym	Active	Case insensitive	SNOMED CT core
3289808012	Albinism co-occurrent with haematologic disorder	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

Unit of use quantity reference set

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