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38576000: Nonfamilial hyperinsulinemic isolated somatotropin deficiency (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
64963016 Nonfamilial hyperinsulinemic isolated somatotropin deficiency en Synonym Active Entire term case insensitive SNOMED CT core module
64964010 Ateliotic dwarfism with hyperinsulinemia en Synonym Active Entire term case insensitive SNOMED CT core module
491305010 Ateliotic dwarfism with hyperinsulinaemia en Synonym Active Entire term case insensitive SNOMED CT core module
491306011 Nonfamilial hyperinsulinaemic isolated somatotropin deficiency en Synonym Active Entire term case insensitive SNOMED CT core module
774488012 Nonfamilial hyperinsulinemic isolated somatotropin deficiency (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Nonfamilial hyperinsulinemic isolated somatotropin deficiency Is a Isolated somatotropin deficiency true Inferred relationship Existential restriction modifier
Nonfamilial hyperinsulinemic isolated somatotropin deficiency Interprets Nutritional deficiency false Inferred relationship Existential restriction modifier
Nonfamilial hyperinsulinemic isolated somatotropin deficiency Finding site Pars anterior of pituitary gland false Inferred relationship Existential restriction modifier
Nonfamilial hyperinsulinemic isolated somatotropin deficiency Finding site Entire endocrine gonad false Inferred relationship Existential restriction modifier
Nonfamilial hyperinsulinemic isolated somatotropin deficiency Finding site Structure of pars distalis of pituitary true Inferred relationship Existential restriction modifier 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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