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237655001: X-linked hypoparathyroidism (disorder)


Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
356186014 Hypoparathyroidism - X-linked en Synonym Active Initial character case insensitive SNOMED CT core
4637475012 X-linked hypoparathyroidism (disorder) en Fully specified name Active Case sensitive SNOMED CT core
4637476013 X-linked hypoparathyroidism en Synonym Active Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


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

Problem/Diagnosis reference set

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