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419097006: Danon disease (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2006. Module: SNOMED CT core module

Descriptions:

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


0 descendants.

Expanded Value Set


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

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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