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237687003: Isolated growth hormone deficiency - autosomal dominant (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
356231015 Autosomal dominant isolated somatotropin deficiency en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
356232010 Isolated growth hormone deficiency - autosomal dominant en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
626450013 Isolated growth hormone deficiency - autosomal dominant (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Autosomal dominant isolated somatotropin deficiency localisation d'une constatation (attribut) Structure of pars distalis of pituitary (body structure) true Inferred relationship Some 1
Autosomal dominant isolated somatotropin deficiency localisation d'une constatation (attribut) Entire endocrine gonad (body structure) false Inferred relationship Some
Autosomal dominant isolated somatotropin deficiency localisation d'une constatation (attribut) Pars anterior of pituitary gland false Inferred relationship Some
Autosomal dominant isolated somatotropin deficiency interprète (attribut) Nutritional deficiency state false Inferred relationship Some
Autosomal dominant isolated somatotropin deficiency est un(e) (attribut) Isolated somatotropin deficiency true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Client's clinical problems, conditions, diagnoses, symptoms, findings, complaints reference set (foundation metadata concept)

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