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1186807002: hereditaire groeihormoondeficiëntie (aandoening)


Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 30-Nov 2021. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
4667738012 Hereditary growth hormone deficiency (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
4667739016 Hereditary growth hormone deficiency en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
13245481000146119 hereditaire groeihormoondeficiëntie nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
13245491000146117 hereditaire groeihormoondeficiëntie (aandoening) nl Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
13306041000146110 erfelijke deficiëntie van groeihormoon nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)


3 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hereditary growth hormone deficiency (disorder) Is a Hereditary disorder of endocrine system (disorder) true Inferred relationship Some
Hereditary growth hormone deficiency (disorder) Is a Hereditary disorder of nervous system true Inferred relationship Some
Hereditary growth hormone deficiency (disorder) Is a Growth hormone deficiency (disorder) true Inferred relationship Some
Hereditary growth hormone deficiency (disorder) Finding site Structure of pars distalis of pituitary (body structure) true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group
Growth delay due to insulin-like growth factor type 1 deficiency (disorder) Is a True Hereditary growth hormone deficiency (disorder) Inferred relationship Some
Cataract, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, skeletal dysplasia syndrome (disorder) Is a True Hereditary growth hormone deficiency (disorder) Inferred relationship Some
Congenital isolated growth hormone deficiency Is a True Hereditary growth hormone deficiency (disorder) Inferred relationship Some

This concept is not in any reference sets

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