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38576000: Nonfamilial hyperinsulinemic isolated somatotropin deficiency (disorder)


Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
491305010 Ateliotic dwarfism with hyperinsulinaemia en Synonym Active Case insensitive SNOMED CT core
491306011 Nonfamilial hyperinsulinaemic isolated somatotropin deficiency en Synonym Active Case insensitive SNOMED CT core
64963016 Nonfamilial hyperinsulinemic isolated somatotropin deficiency en Synonym Active Case insensitive SNOMED CT core
64964010 Ateliotic dwarfism with hyperinsulinemia en Synonym Active Case insensitive SNOMED CT core
774488012 Nonfamilial hyperinsulinemic isolated somatotropin deficiency (disorder) en Fully specified name Active Case insensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Nonfamilial hyperinsulinaemic isolated somatotropin deficiency Is a Isolated somatotropin deficiency true Inferred relationship Some
Nonfamilial hyperinsulinaemic isolated somatotropin deficiency Finding site Structure of distal part of pituitary true Inferred relationship Some 1
Nonfamilial hyperinsulinaemic isolated somatotropin deficiency Interprets Nutritional deficiency false Inferred relationship Some
Nonfamilial hyperinsulinaemic isolated somatotropin deficiency Finding site Pars anterior of pituitary gland false Inferred relationship Some
Nonfamilial hyperinsulinaemic isolated somatotropin deficiency Finding site Entire endocrine gonad false Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Australian dialect reference set

Problem/Diagnosis reference set

Description inactivation indicator reference set

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