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83911000119104: Severe obesity (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2016. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3289704018 Severe obesity en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3289802013 Severe obesity (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core


5 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Severe obesity Is a Obesity (disorder) true Inferred relationship Some
Severe obesity Has definitional manifestation Obese (finding) false Inferred relationship Some
Severe obesity Interprets Body weight measure true Inferred relationship Some 1
Severe obesity Has interpretation Above reference range (qualifier value) true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group
Severe obesity complicating pregnancy Is a True Severe obesity Inferred relationship Some
A rare genetic form of obesity characterised by severe early-onset obesity, hyperphagia, insulin resistance with hyperinsulinaemia, reduced adult final height, delayed speech and language development and a tendency for social isolation and aggressive behaviour. Is a True Severe obesity Inferred relationship Some
A rare genetic form of obesity with characteristics of severe early-onset obesity, hyperphagia and variable presence of cognitive impairment and behavioral disorder, including autistic spectrum behavior, impaired concentration and memory deficit. Some patients present with Prader-Willi-like features such as hypotonia, developmental delay, intellectual disability, short stature, hypopituitarism and dysmorphic facial features. Is a True Severe obesity Inferred relationship Some
A rare genetic non-syndromic obesity disease with characteristics of severe early-onset obesity associated with major hyperphagia and endocrine abnormalities resulting from leptin receptor deficiency. Caused by homozygous mutation in the gene encoding the leptin receptor (LEPR) on chromosome 1p31. Is a True Severe obesity Inferred relationship Some
A rare syndromic obesity characterized by early-onset severe obesity, hyperphagia and global developmental delay with specific impairment of short term memory and language delay. Patients may represent moderate intellectual disability, stereotyped behaviors, autistic features, impaired nociception, hypotonia and seizures. Facial asymmetry and streak ovaries were also reported in a few cases. Is a True Severe obesity Inferred relationship Some

This concept is not in any reference sets

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