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38196001: Laron-type isolated somatotropin defect (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
4535149016 Laron syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
63917019 Laron-type isolated somatotropin defect en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
63918012 Laron-type dwarfism en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
63919016 Laron dwarfism en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
63920010 Laron-type pituitary dwarfism en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
771912011 Laron-type isolated somatotropin defect (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core

2 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Laron-type isolated somatotropin defect Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Laron-type isolated somatotropin defect est un(e) (attribut) Developmental hereditary disorder true Inferred relationship Some
Laron-type isolated somatotropin defect interprète (attribut) Height / growth measure true Inferred relationship Some 2
Laron-type isolated somatotropin defect est un(e) (attribut) nanisme hypophysaire false Inferred relationship Some
Laron-type isolated somatotropin defect est un(e) (attribut) insuffisance staturale true Inferred relationship Some
Laron-type isolated somatotropin defect localisation d'une constatation (attribut) Adenohypophysis structure false Inferred relationship Some
Laron-type isolated somatotropin defect survenue (attribut) congénital false Inferred relationship Some
Laron-type isolated somatotropin defect est un(e) (attribut) Autosomal recessive hereditary disorder true Inferred relationship Some
Laron-type isolated somatotropin defect est un(e) (attribut) True dwarfism false Inferred relationship Some
Laron-type isolated somatotropin defect morphologie associée (attribut) Developmental abnormality false Inferred relationship Some
Laron-type isolated somatotropin defect interprète (attribut) Nutritional deficiency state false Inferred relationship Some
Laron-type isolated somatotropin defect localisation d'une constatation (attribut) Pars anterior of pituitary gland false Inferred relationship Some
Laron-type isolated somatotropin defect morphologie associée (attribut) Congenital deficiency false Inferred relationship Some
Laron-type isolated somatotropin defect localisation d'une constatation (attribut) Entire endocrine gonad (body structure) false Inferred relationship Some
Inbound Relationships Type Active Source Characteristic Refinability Group
Growth hormone receptor absent est un(e) (attribut) True Laron-type isolated somatotropin defect Inferred relationship Some
Growth hormone receptor abnormality est un(e) (attribut) True Laron-type isolated somatotropin defect Inferred relationship Some

Reference Sets

Canada English language reference set (foundation metadata concept)

Client's clinical problems, conditions, diagnoses, symptoms, findings, complaints reference set (foundation metadata concept)

Description inactivation indicator reference set

GB English

US English

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