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237653008: Familial primary hyperparathyroidism (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
356183018 Familial hyperparathyroidism en Synonym Active Entire term case insensitive SNOMED CT core module
356184012 Familial primary hyperparathyroidism en Synonym Active Entire term case insensitive SNOMED CT core module
626412019 Familial primary hyperparathyroidism (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module

2 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Familial primary hyperparathyroidism Is a Primary hyperparathyroidism true Inferred relationship Existential restriction modifier
Familial primary hyperparathyroidism Finding site Parathyroid structure true Inferred relationship Existential restriction modifier 2
Familial primary hyperparathyroidism Finding site Entire endocrine gonad false Inferred relationship Existential restriction modifier
Familial primary hyperparathyroidism Has definitional manifestation Increased hormone secretion false Inferred relationship Existential restriction modifier
Familial primary hyperparathyroidism Has interpretation Increased true Inferred relationship Existential restriction modifier 1
Familial primary hyperparathyroidism Interprets Hormone secretion, function true Inferred relationship Existential restriction modifier 1
Inbound Relationships Type Active Source Characteristic Refinability Group
Hyperparathyroidism-jaw tumor syndrome Is a True Familial primary hyperparathyroidism Inferred relationship Existential restriction modifier
Familial isolated hyperparathyroidism Is a True Familial primary hyperparathyroidism Inferred relationship Existential restriction modifier

This concept is not in any reference sets

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