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

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

Descriptions:

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

0 descendants.

Expanded Value Set

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

This concept is not in any reference sets

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