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71578002: Steroid 21-monooxygenase deficiency, salt wasting type (disorder)

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2016. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
118912012 Steroid 21-monooxygenase deficiency, salt wasting type en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
118913019 Congenital adrenal hyperplasia, type 2 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
200220011 21-hydroxylase deficiency, salt wasting type en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
811759010 Steroid 21-monooxygenase deficiency, salt wasting type (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
118912012 Steroid 21-monooxygenase deficiency, salt wasting type en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
118912012 Steroid 21-monooxygenase deficiency, salt wasting type en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
118913019 Congenital adrenal hyperplasia, type 2 en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
118913019 Congenital adrenal hyperplasia, type 2 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
200220011 21-hydroxylase deficiency, salt wasting type en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
200220011 21-hydroxylase deficiency, salt wasting type en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
200220011 21-hydroxylase deficiency, salt wasting type en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
811759010 Steroid 21-monooxygenase deficiency, salt wasting type (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
811759010 Steroid 21-monooxygenase deficiency, salt wasting type (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Steroid 21-monooxygenase deficiency, salt wasting type (disorder) Is a Salt-losing congenital adrenal hyperplasia (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Steroid 21-monooxygenase deficiency, salt wasting type (disorder) Finding site Adrenal cortex structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Steroid 21-monooxygenase deficiency, salt wasting type (disorder) Finding site Entire endocrine gonad (body structure) false Inferred relationship Existential restriction modifier (core metadata concept)
Steroid 21-monooxygenase deficiency, salt wasting type (disorder) Associated morphology Congenital hyperplasia false Inferred relationship Existential restriction modifier (core metadata concept) 1
Steroid 21-monooxygenase deficiency, salt wasting type (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Steroid 21-monooxygenase deficiency, salt wasting type (disorder) Is a Deficiency of steroid 21-monooxygenase false Inferred relationship Existential restriction modifier (core metadata concept)
Steroid 21-monooxygenase deficiency, salt wasting type (disorder) Associated morphology Hyperplasia true Inferred relationship Existential restriction modifier (core metadata concept) 1
Steroid 21-monooxygenase deficiency, salt wasting type (disorder) Is a Congenital anomaly of adrenal gland false Inferred relationship Existential restriction modifier (core metadata concept)
Steroid 21-monooxygenase deficiency, salt wasting type (disorder) Associated morphology Congenital hyperplasia false Inferred relationship Existential restriction modifier (core metadata concept) 3
Steroid 21-monooxygenase deficiency, salt wasting type (disorder) Finding site Adrenal cortex structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Steroid 21-monooxygenase deficiency, salt wasting type (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 3
Steroid 21-monooxygenase deficiency, salt wasting type (disorder) Associated morphology Hyperplasia false Inferred relationship Existential restriction modifier (core metadata concept) 2
Steroid 21-monooxygenase deficiency, salt wasting type (disorder) Finding site Adrenal cortex structure false Inferred relationship Existential restriction modifier (core metadata concept) 3
Steroid 21-monooxygenase deficiency, salt wasting type (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Steroid 21-monooxygenase deficiency, salt wasting type (disorder) Finding site Adrenal cortex structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Steroid 21-monooxygenase deficiency, salt wasting type (disorder) Due to 21-hydroxylase deficiency false Inferred relationship Existential restriction modifier (core metadata concept)
Steroid 21-monooxygenase deficiency, salt wasting type (disorder) Is a Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Steroid 21-monooxygenase deficiency, salt wasting type (disorder) Due to Deficiency of steroid 21-monooxygenase true Inferred relationship Existential restriction modifier (core metadata concept) 2
Steroid 21-monooxygenase deficiency, salt wasting type (disorder) Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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