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1217515007: Autosomal dominant familial isolated hypoparathyroidism (disorder)


Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 30-Apr 2022. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
5036553015 Autosomal dominant familial isolated hypoparathyroidism (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
5036554014 Autosomal dominant familial isolated hypoparathyroidism en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Autosomal dominant familial isolated hypoparathyroidism (disorder) est un(e) (attribut) Autosomal dominant hereditary disorder true Inferred relationship Some
Autosomal dominant familial isolated hypoparathyroidism (disorder) est un(e) (attribut) Familial isolated hypoparathyroidism (disorder) true Inferred relationship Some
Autosomal dominant familial isolated hypoparathyroidism (disorder) localisation d'une constatation (attribut) Parathyroid structure true Inferred relationship Some 2
Autosomal dominant familial isolated hypoparathyroidism (disorder) interprète (attribut) Hormone secretion true Inferred relationship Some 1
Autosomal dominant familial isolated hypoparathyroidism (disorder) a pour interprétation (attribut) Decreased true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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