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111941005: Familial disease (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
179087019 Familial disease en Synonym Active Entire term case insensitive SNOMED CT core module
635166017 Familial disease (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module

157 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Familial disease Is a Disease true Inferred relationship Existential restriction modifier
Inbound Relationships Type Active Source Characteristic Refinability Group
Familial patent arterial duct Is a True Familial disease Inferred relationship Existential restriction modifier
Familial hyperreninemic hypoaldosteronism type 2 Is a False Familial disease Inferred relationship Existential restriction modifier
Familial atrial tachyarrhythmia, infra-Hisian cardiac conduction disease Is a True Familial disease Inferred relationship Existential restriction modifier
Familial chylomicronemia syndrome Is a True Familial disease Inferred relationship Existential restriction modifier
Familial cerebral saccular aneurysm Is a True Familial disease Inferred relationship Existential restriction modifier
Familial hyperreninemic hypoaldosteronism type 1B Is a True Familial disease Inferred relationship Existential restriction modifier
Familial congenital nasolacrimal duct obstruction Is a True Familial disease Inferred relationship Existential restriction modifier
Familial intestinal malrotation Is a True Familial disease Inferred relationship Existential restriction modifier
Familial juvenile gout Is a True Familial disease Inferred relationship Existential restriction modifier

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This concept is not in any reference sets

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