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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
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
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 Only initial character case insensitive (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
4535149016 Laron syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3385111001000110 Laron-Syndrom de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
4514721000241111 anomalie génétique du récepteur de la somatotropine - type Laron fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
4514721000241111 anomalie génétique du récepteur de la somatotropine - type Laron fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3385111001000110 Laron-Syndrom de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

2 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Laron-type isolated somatotropin defect Is a Pituitary dwarfism false Inferred relationship Existential restriction modifier (core metadata concept)
Laron-type isolated somatotropin defect Is a Short stature disorder (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Laron-type isolated somatotropin defect Associated morphology anomalie du développement false Inferred relationship Existential restriction modifier (core metadata concept)
Laron-type isolated somatotropin defect Interprets Nutritional deficiency state false Inferred relationship Existential restriction modifier (core metadata concept)
Laron-type isolated somatotropin defect Finding site Pars anterior of pituitary gland false Inferred relationship Existential restriction modifier (core metadata concept)
Laron-type isolated somatotropin defect Associated morphology Congenital deficiency false Inferred relationship Existential restriction modifier (core metadata concept)
Laron-type isolated somatotropin defect Finding site Entire endocrine gonad (body structure) false Inferred relationship Existential restriction modifier (core metadata concept)
Laron-type isolated somatotropin defect Finding site Adenohypophysis structure false Inferred relationship Existential restriction modifier (core metadata concept)
Laron-type isolated somatotropin defect Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Laron-type isolated somatotropin defect Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Laron-type isolated somatotropin defect Is a Dwarfism false Inferred relationship Existential restriction modifier (core metadata concept)
Laron-type isolated somatotropin defect Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Laron-type isolated somatotropin defect Is a Developmental hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Laron-type isolated somatotropin defect Interprets Height / growth measure (observable entity) true Inferred relationship Existential restriction modifier (core metadata concept) 2
Inbound Relationships Type Active Source Characteristic Refinability Group
Growth hormone receptor absent Is a True Laron-type isolated somatotropin defect Inferred relationship Existential restriction modifier (core metadata concept)
Growth hormone receptor abnormality (disorder) Is a True Laron-type isolated somatotropin defect Inferred relationship Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

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