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1217515007: Autosomal dominant familial isolated hypoparathyroidism (disorder)


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

Descriptions:

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


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Autosomal dominant familial isolated hypoparathyroidism Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier
Autosomal dominant familial isolated hypoparathyroidism Is a Familial isolated hypoparathyroidism true Inferred relationship Existential restriction modifier
Autosomal dominant familial isolated hypoparathyroidism Finding site Parathyroid structure true Inferred relationship Existential restriction modifier 2
Autosomal dominant familial isolated hypoparathyroidism Interprets Hormone secretion, function true Inferred relationship Existential restriction modifier 1
Autosomal dominant familial isolated hypoparathyroidism Has interpretation Decreased true Inferred relationship Existential restriction modifier 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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