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765326001: Familial glucocorticoid deficiency (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2018. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3657918013 Familial glucocorticoid deficiency (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3657919017 Familial glucocorticoid deficiency 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
Familial glucocorticoid deficiency Is a Hereditary disorder of endocrine system false Inferred relationship Existential restriction modifier
Familial glucocorticoid deficiency Finding site Adrenal cortex structure true Inferred relationship Existential restriction modifier 1
Familial glucocorticoid deficiency Occurrence Congenital false Inferred relationship Existential restriction modifier 1
Familial glucocorticoid deficiency Is a Adrenal cortical hypofunction false Inferred relationship Existential restriction modifier
Familial glucocorticoid deficiency Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier
Familial glucocorticoid deficiency Occurrence Congenital true Inferred relationship Existential restriction modifier 2
Familial glucocorticoid deficiency Is a Adrenocorticotropic hormone resistance syndrome true Inferred relationship Existential restriction modifier
Familial glucocorticoid deficiency Finding site Thyroid structure true Inferred relationship Existential restriction modifier 2
Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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