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237785004: Hypoadrenalism (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
356349017 Hypoadrenalism en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
626562014 Hypoadrenalism (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3506672018 Adrenal hypofunction en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
2026701000005118 Hypoadrenalisme da Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Danish module (core metadata concept)


60 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hypoadrenalism Is a Disorder of adrenal gland true Inferred relationship Some
Hypoadrenalism Finding site Entire endocrine gonad (body structure) false Inferred relationship Some
Hypoadrenalism Finding site Adrenal structure true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group
ACTH deficiency Is a True Hypoadrenalism Inferred relationship Some
Adrenal hypofunktion Is a False Hypoadrenalism Inferred relationship Some
Severe adrenal insufficiency Is a False Hypoadrenalism Inferred relationship Some
Waterhouse-Friderichsen syndrome Is a False Hypoadrenalism Inferred relationship Some
Adrenal medullary insufficiency Is a True Hypoadrenalism Inferred relationship Some
Adrenal cortical hypofunction (disorder) Is a True Hypoadrenalism Inferred relationship Some
A primary adrenal insufficiency caused by a sudden defective production of adrenal steroids (cortisol and aldosterone). It represents an emergency, thus the rapid recognition and prompt therapy are critical for survival even before the diagnosis is made. Is a False Hypoadrenalism Inferred relationship Some
A rare genetic developmental defect during embryogenesis disorder with characteristics of severe early-onset salt-wasting adrenal insufficiency and ambiguous/female external genitalia (irrespective of chromosomal sex) due to mutations in the CYP11A1 gene. Milder cases may present delayed onset of adrenal gland dysfunction and genitalia phenotype may range from normal male to female in individuals with 46,XY karyotype. Imaging studies reveal hypoplastic/absent adrenal glands and biochemical findings include low serum cortisol, mineralocorticoids, androgens and sodium with elevated potassium levels. Caused by heterozygous, compound heterozygous or homozygous mutation in the CYP11A1 gene on chromosome 15q23-q24. Is a True Hypoadrenalism Inferred relationship Some
Hypoadrenalism due to paracoccidioidomycosis (disorder) Is a True Hypoadrenalism Inferred relationship Some

This concept is not in any reference sets

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