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1186807002: Hereditary growth hormone deficiency (disorder)


Status: current, Defined. 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 Case insensitive SNOMED CT core
4667739016 Hereditary growth hormone deficiency en Synonym Active Case insensitive SNOMED CT core


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 Some
Hereditary growth hormone deficiency Is a Hereditary disorder of nervous system true Inferred relationship Some
Hereditary growth hormone deficiency Is a Growth hormone deficiency true Inferred relationship Some
Hereditary growth hormone deficiency Finding site Structure of distal part of pituitary true Inferred relationship Some 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 Some
Cataract, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, skeletal dysplasia syndrome Is a True Hereditary growth hormone deficiency Inferred relationship Some

Reference Sets

Clinical finding foundation reference set

Problem/Diagnosis reference set

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