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45235005: Mild steroid 21-hydroxylase deficiency (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
75420016 Mild steroid 21-hydroxylase deficiency en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
782452013 Mild steroid 21-hydroxylase deficiency (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
75420016 Mild steroid 21-hydroxylase deficiency en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
75420016 Mild steroid 21-hydroxylase deficiency en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
782452013 Mild steroid 21-hydroxylase deficiency (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
782452013 Mild steroid 21-hydroxylase deficiency (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
4537731000241112 déficit léger en stéroïde 21-hydroxylase fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
4537731000241112 déficit léger en stéroïde 21-hydroxylase 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
Mild steroid 21-hydroxylase deficiency Is a Steroid 21-monooxygenase deficiency, simple virilizing type false Inferred relationship Existential restriction modifier (core metadata concept)
Mild steroid 21-hydroxylase deficiency Is a Deficiency of steroid 21-monooxygenase true Inferred relationship Existential restriction modifier (core metadata concept)
Mild steroid 21-hydroxylase deficiency Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Mild steroid 21-hydroxylase deficiency Associated morphology Glandular hyperplasia false Inferred relationship Existential restriction modifier (core metadata concept)
Mild steroid 21-hydroxylase deficiency Finding site Adrenal cortex structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Mild steroid 21-hydroxylase deficiency Finding site Entire endocrine gonad (body structure) false Inferred relationship Existential restriction modifier (core metadata concept)
Mild steroid 21-hydroxylase deficiency Associated morphology Congenital hyperplasia false Inferred relationship Existential restriction modifier (core metadata concept) 1
Mild steroid 21-hydroxylase deficiency Severity Mild false 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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