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419097006: Danon disease (disorder)


Status: current, Primitive. Date: 31-Jan 2006. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
2574361014 Danon disease (disorder) en Fully specified name Active Case sensitive SNOMED CT core
2577707016 Danon disease en Synonym Active Case sensitive SNOMED CT core
4634468019 Glycogenosis due to LAMP-2 deficiency en Synonym Active Initial character case insensitive SNOMED CT core
4634469010 Lysosomal glycogen storage disease with normal acid maltase activity en Synonym Active Case insensitive SNOMED CT core
4634470011 Glycogen storage disease due to LAMP-2 deficiency en Synonym Active Initial character case insensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Danon disease Is a X-linked recessive hereditary disease true Inferred relationship Some
Danon disease Is a Cardiomyopathy true Inferred relationship Some
Danon disease Is a X-linked hereditary disease false Inferred relationship Some
Danon disease Is a Cardiovascular system hereditary disorder true Inferred relationship Some
Danon disease Is a Multisystem disorder false Inferred relationship Some
Danon disease Is a Glycogen storage disease true Inferred relationship Some
Danon disease Finding site Myocardium structure true Inferred relationship Some 2
Danon disease Occurrence Congenital true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Cardiovascular finding reference set

Problem/Diagnosis reference set

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