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3652007: Overproduction of growth hormone (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
7168017 Overproduction of growth hormone en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
7170014 Hypersomatotropism en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
768282016 Overproduction of growth hormone (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
1742461000005110 Overproduktion af væksthormon da Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Danish module (core metadata concept)


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Overproduction of growth hormone (disorder) Is a Hyperpituitarism true Inferred relationship Some
Overproduction of growth hormone (disorder) Finding site Entire endocrine gonad (body structure) false Inferred relationship Some
Overproduction of growth hormone (disorder) Finding site Pars anterior of pituitary gland false Inferred relationship Some
Overproduction of growth hormone (disorder) Interprets Increased hormone secretion false Inferred relationship Some
Overproduction of growth hormone (disorder) Finding site Adenohypophysis structure true Inferred relationship Some 2
Overproduction of growth hormone (disorder) Has definitional manifestation Increased hormone production false Inferred relationship Some
Overproduction of growth hormone (disorder) Has interpretation Increased true Inferred relationship Some 1
Overproduction of growth hormone (disorder) Interprets Hormone production true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group
A rare genetic endocrine disease with characteristics of early-onset (before the age of five years old) excessive acceleration of linear growth and body size due to pituitary mixed growth hormone and prolactin secreting adenomas and/or mixed-cell pituitary hyperplasia. Patients present gigantism and may associate acromegalic features (for example coarse facial features, frontal bossing, prognathism, increased interdental space) as well as marked enlargement of hands and feet, soft tissue swelling, appetite increase and acanthosis nigricans. Due to True Overproduction of growth hormone (disorder) Inferred relationship Some 3
A type of familial infantile gigantism caused by microduplication of Xq26.3. Onset usually occurs in the first year of life in previously normal infants. Patients present with gigantism and may associate acromegalic features (e.g. coarse facial features, frontal bossing, prognathism, increased interdental space) as well as marked enlargement of hands and feet, soft tissue swelling, appetite increase and acanthosis nigricans. May present as a sporadic condition or as familial isolated pituitary adenomas. Due to True Overproduction of growth hormone (disorder) Inferred relationship Some 3
Hypersomatotropic gigantism Due to True Overproduction of growth hormone (disorder) Inferred relationship Some 1

This concept is not in any reference sets

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