FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.13  |  FHIR Version n/a  User: [n/a]

702949005: Proopiomelanocortin deficiency syndrome (disorder)


Status: current, Primitive. Date: 31-Jul 2014. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3006608012 Obesity, early-onset, adrenal insufficiency, and red hair en Synonym Active Case insensitive SNOMED CT core
3006609016 Proopiomelanocortin deficiency syndrome en Synonym Active Case insensitive SNOMED CT core
3006616015 Proopiomelanocortin deficiency syndrome (disorder) en Fully specified name Active Case insensitive SNOMED CT core
3007005019 Proopiomelanocortin deficiency causes severe obesity beginning at an early age. Affected individuals also have low levels of adrenocorticotropic hormone (ACTH) and tend to have red hair and pale skin. en Definition Active Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Proopiomelanocortin deficiency syndrome Has interpretation Above reference range true Inferred relationship Some 1
Proopiomelanocortin deficiency syndrome Is a Morbid obesity true Inferred relationship Some
Proopiomelanocortin deficiency syndrome Is a ACTH deficiency true Inferred relationship Some
Proopiomelanocortin deficiency syndrome Finding site Adrenal structure true Inferred relationship Some 3
Proopiomelanocortin deficiency syndrome Finding site Structure of distal part of pituitary true Inferred relationship Some 2
Proopiomelanocortin deficiency syndrome Has definitional manifestation Obese false Inferred relationship Some
Proopiomelanocortin deficiency syndrome Interprets Body weight measure true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

Back to Start