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1186807002: Hereditary growth hormone deficiency (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
4667738012 Hereditary growth hormone deficiency (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
4667739016 Hereditary growth hormone deficiency en Synonym Active Entire term case insensitive SNOMED CT core module


2 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hereditary growth hormone deficiency Is a Hereditary disorder of endocrine system true Inferred relationship Existential restriction modifier
Hereditary growth hormone deficiency Is a Hereditary disorder of nervous system true Inferred relationship Existential restriction modifier
Hereditary growth hormone deficiency Is a Growth hormone deficiency true Inferred relationship Existential restriction modifier
Hereditary growth hormone deficiency Finding site Structure of pars distalis of pituitary true Inferred relationship Existential restriction modifier 1

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

This concept is not in any reference sets

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