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237687003: Isolated growth hormone deficiency - autosomal dominant (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
356231015 Autosomal dominant isolated somatotropin deficiency en Synonym Active Entire term case insensitive SNOMED CT core module
356232010 Isolated growth hormone deficiency - autosomal dominant en Synonym Active Entire term case insensitive SNOMED CT core module
626450013 Isolated growth hormone deficiency - autosomal dominant (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
Isolated growth hormone deficiency - autosomal dominant Is a Isolated somatotropin deficiency true Inferred relationship Existential restriction modifier
Isolated growth hormone deficiency - autosomal dominant Finding site Entire endocrine gonad false Inferred relationship Existential restriction modifier
Isolated growth hormone deficiency - autosomal dominant Finding site Pars anterior of pituitary gland false Inferred relationship Existential restriction modifier
Isolated growth hormone deficiency - autosomal dominant Interprets Nutritional deficiency false Inferred relationship Existential restriction modifier
Isolated growth hormone deficiency - autosomal dominant 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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