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237655001: X-linked hypoparathyroidism (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
356186014 Hypoparathyroidism - X-linked en Synonym Active Only initial character case insensitive SNOMED CT core module
4637475012 X-linked hypoparathyroidism (disorder) en Fully specified name Active Entire term case sensitive SNOMED CT core module
4637476013 X-linked hypoparathyroidism en Synonym Active Entire term case sensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
X-linked hypoparathyroidism Is a Hypoparathyroidism true Inferred relationship Existential restriction modifier
X-linked hypoparathyroidism Finding site Parathyroid structure true Inferred relationship Existential restriction modifier 2
X-linked hypoparathyroidism Interprets Nutritional deficiency false Inferred relationship Existential restriction modifier
X-linked hypoparathyroidism Finding site Entire endocrine gonad false Inferred relationship Existential restriction modifier
X-linked hypoparathyroidism Has definitional manifestation Decreased hormone secretion false Inferred relationship Existential restriction modifier
X-linked hypoparathyroidism Has interpretation Decreased true Inferred relationship Existential restriction modifier 1
X-linked hypoparathyroidism Interprets Hormone secretion, function true Inferred relationship Existential restriction modifier 1
X-linked hypoparathyroidism Is a X-linked hereditary disease true Inferred relationship Existential restriction modifier
X-linked hypoparathyroidism Is a Hereditary disorder of endocrine system 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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