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18200000: Autosomal recessive isolated somatotropin deficiency (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
30739018 Autosomal recessive isolated somatotropin deficiency en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
30740016 Isolated growth hormone deficiency type I en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
30741017 Pituitary dwarfism type I en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
745590012 Autosomal recessive isolated somatotropin deficiency (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
30739018 Autosomal recessive isolated somatotropin deficiency en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
30739018 Autosomal recessive isolated somatotropin deficiency en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
30740016 Isolated growth hormone deficiency type I en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
30741017 Pituitary dwarfism type I en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
745590012 Autosomal recessive isolated somatotropin deficiency (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
745590012 Autosomal recessive isolated somatotropin deficiency (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
5809611000241115 déficit autosomique récessif isolé en somatotropine fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5809631000241112 nanisme hypophysaire de type 1 fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5809651000241116 déficit isolé en hormone de croissance de type I fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5809611000241115 déficit autosomique récessif isolé en somatotropine fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5809631000241112 nanisme hypophysaire de type 1 fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5809651000241116 déficit isolé en hormone de croissance de type I fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Autosomal recessive isolated somatotropin deficiency Is a Pituitary dwarfism true Inferred relationship Existential restriction modifier (core metadata concept)
Autosomal recessive isolated somatotropin deficiency Is a Isolated somatotropin deficiency true Inferred relationship Existential restriction modifier (core metadata concept)
Autosomal recessive isolated somatotropin deficiency Finding site Entire endocrine gonad (body structure) false Inferred relationship Existential restriction modifier (core metadata concept)
Autosomal recessive isolated somatotropin deficiency Finding site Pars anterior of pituitary gland false Inferred relationship Existential restriction modifier (core metadata concept)
Autosomal recessive isolated somatotropin deficiency Interprets Nutritional deficiency state false Inferred relationship Existential restriction modifier (core metadata concept)
Autosomal recessive isolated somatotropin deficiency Associated morphology Congenital deficiency false Inferred relationship Existential restriction modifier (core metadata concept)
Autosomal recessive isolated somatotropin deficiency Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Autosomal recessive isolated somatotropin deficiency Finding site Structure of distal part of pituitary true Inferred relationship Existential restriction modifier (core metadata concept) 1
Autosomal recessive isolated somatotropin deficiency Pathological process (attribute) Pathological developmental process (qualifier value) false Inferred relationship Existential restriction modifier (core metadata concept) 2
Autosomal recessive isolated somatotropin deficiency Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Autosomal recessive isolated somatotropin deficiency Due to Growth hormone deficiency (disorder) true Inferred relationship Existential restriction modifier (core metadata concept) 2
Autosomal recessive isolated somatotropin deficiency Interprets Height / growth measure (observable entity) true Inferred relationship Existential restriction modifier (core metadata concept) 3

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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