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38196001: Laron-type isolated somatotropin defect (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
63917019 Laron-type isolated somatotropin defect en Synonym Active Entire term case sensitive SNOMED CT core module
63918012 Laron-type dwarfism en Synonym Active Entire term case sensitive SNOMED CT core module
63919016 Laron dwarfism en Synonym Active Entire term case sensitive SNOMED CT core module
63920010 Laron-type pituitary dwarfism en Synonym Active Entire term case sensitive SNOMED CT core module
771912011 Laron-type isolated somatotropin defect (disorder) en Fully specified name Active Entire term case sensitive SNOMED CT core module
4535149016 Laron syndrome en Synonym Active Entire term case sensitive SNOMED CT core 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
Laron-type isolated somatotropin defect Is a Short stature disorder true Inferred relationship Existential restriction modifier
Laron-type isolated somatotropin defect Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier
Laron-type isolated somatotropin defect Interprets Nutritional deficiency false Inferred relationship Existential restriction modifier
Laron-type isolated somatotropin defect Finding site Pars anterior of pituitary gland false Inferred relationship Existential restriction modifier
Laron-type isolated somatotropin defect Associated morphology Congenital deficiency false Inferred relationship Existential restriction modifier
Laron-type isolated somatotropin defect Finding site Entire endocrine gonad false Inferred relationship Existential restriction modifier
Laron-type isolated somatotropin defect Finding site Adenohypophysis structure false Inferred relationship Existential restriction modifier
Laron-type isolated somatotropin defect Occurrence Congenital false Inferred relationship Existential restriction modifier
Laron-type isolated somatotropin defect Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier
Laron-type isolated somatotropin defect Is a Dwarfism false Inferred relationship Existential restriction modifier
Laron-type isolated somatotropin defect Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Laron-type isolated somatotropin defect Is a Developmental hereditary disorder true Inferred relationship Existential restriction modifier
Laron-type isolated somatotropin defect Interprets Height / growth measure true Inferred relationship Existential restriction modifier 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
Growth hormone receptor abnormality Is a True Laron-type isolated somatotropin defect Inferred relationship Existential restriction modifier

This concept is not in any reference sets

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