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786037006: Familial isolated hyperparathyroidism (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2019. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3770071010 Familial isolated hyperparathyroidism (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3770072015 Familial isolated hyperparathyroidism en Synonym Active Entire term case insensitive SNOMED CT core module
3770073013 FIHPT - familial isolated hyperparathyroidism 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
Familial isolated hyperparathyroidism Interprets Hormone secretion, function true Inferred relationship Existential restriction modifier 1
Familial isolated hyperparathyroidism Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier
Familial isolated hyperparathyroidism Is a Familial primary hyperparathyroidism true Inferred relationship Existential restriction modifier
Familial isolated hyperparathyroidism Has interpretation Increased true Inferred relationship Existential restriction modifier 1
Familial isolated hyperparathyroidism Is a Hereditary disorder by system false Inferred relationship Existential restriction modifier
Familial isolated hyperparathyroidism Finding site Parathyroid structure true Inferred relationship Existential restriction modifier 2
Familial isolated hyperparathyroidism Due to Neoplasm of parathyroid gland true Inferred relationship Existential restriction modifier 3
Familial isolated hyperparathyroidism 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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