FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.4-SNAPSHOT  |  FHIR Version n/a  User: [n/a]

237655001: X-linked hypoparathyroidism (disorder)

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

Descriptions:

Id Description Lang Type Status Case? Module
356186014 Hypoparathyroidism - X-linked en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
4637475012 X-linked hypoparathyroidism (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
4637476013 X-linked hypoparathyroidism en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
356186014 Hypoparathyroidism - X-linked en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
626415017 Hypoparathyroidism - X-linked (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
4637475012 X-linked hypoparathyroidism (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
4637476013 X-linked hypoparathyroidism en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
5019361000241114 hypoparathyroïdie liée au chromosome X fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5019361000241114 hypoparathyroïdie liée au chromosome X fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

0 descendants.

Expanded Value Set

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

This concept is not in any reference sets

Back to Start