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37495007: Familial adrenocortical hypoplasia (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
62535012 Familial adrenocortical hypoplasia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
62536013 Familial Addison disease en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
62537016 Familial cytomegalic adrenocortical hypoplasia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
769367015 Familial adrenocortical hypoplasia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
62535012 Familial adrenocortical hypoplasia en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
62535012 Familial adrenocortical hypoplasia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
62536013 Familial Addison disease en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
62537016 Familial cytomegalic adrenocortical hypoplasia en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
62537016 Familial cytomegalic adrenocortical hypoplasia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
769367015 Familial adrenocortical hypoplasia (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
769367015 Familial adrenocortical hypoplasia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
66611000077111 hypoplasie corticosurrénale familiale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
66611000077111 hypoplasie corticosurrénale familiale fr Synonym (core metadata concept) Active Entire term 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
Familial adrenocortical hypoplasia Is a Adrenal cortical hypofunction false Inferred relationship Existential restriction modifier (core metadata concept)
Familial adrenocortical hypoplasia Is a Reproductive system hereditary disorder (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
Familial adrenocortical hypoplasia Is a Hereditary disorder of endocrine system (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Familial adrenocortical hypoplasia Is a Familial disease true Inferred relationship Existential restriction modifier (core metadata concept)
Familial adrenocortical hypoplasia Finding site Adrenal cortex structure false Inferred relationship Existential restriction modifier (core metadata concept)
Familial adrenocortical hypoplasia Associated morphology Hypoplasia false Inferred relationship Existential restriction modifier (core metadata concept)
Familial adrenocortical hypoplasia Finding site Entire endocrine gonad (body structure) false Inferred relationship Existential restriction modifier (core metadata concept)
Familial adrenocortical hypoplasia Is a Adrenal cortical hypofunction (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
Familial adrenocortical hypoplasia Is a Congenital hypoplasia of adrenal gland (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Familial adrenocortical hypoplasia Associated morphology Hypoplasia true Inferred relationship Existential restriction modifier (core metadata concept) 1
Familial adrenocortical hypoplasia Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Familial adrenocortical hypoplasia Finding site Adrenal cortex structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Familial adrenocortical hypoplasia Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Familial adrenocortical hypoplasia Is a Developmental hereditary 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

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