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770680004: Prader-Willi-like syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2019. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3702087010 Prader-Willi-like syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
3702088017 Prader-Willi-like syndrome (disorder) en Fully specified name Active Entire term case sensitive SNOMED CT core module


3 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Prader-Willi-like syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 2
Prader-Willi-like syndrome Interprets Measured body weight true Inferred relationship Existential restriction modifier 4
Prader-Willi-like syndrome Is a Obesity true Inferred relationship Existential restriction modifier
Prader-Willi-like syndrome Finding site Gonadal endocrine structure true Inferred relationship Existential restriction modifier 3
Prader-Willi-like syndrome Is a Multiple malformation syndrome with facial defects as major feature true Inferred relationship Existential restriction modifier
Prader-Willi-like syndrome Is a Multiple malformation syndrome with unusual brain and/or neuromuscular findings true Inferred relationship Existential restriction modifier
Prader-Willi-like syndrome Is a Congenital hypogonadotropic hypogonadism true Inferred relationship Existential restriction modifier
Prader-Willi-like syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 3
Prader-Willi-like syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Prader-Willi-like syndrome Finding site Face structure true Inferred relationship Existential restriction modifier 1
Prader-Willi-like syndrome Finding site Structure of pars distalis of pituitary true Inferred relationship Existential restriction modifier 2
Prader-Willi-like syndrome Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier 1
Prader-Willi-like syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Prader-Willi-like syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 3
Prader-Willi-like syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 2
Prader-Willi-like syndrome Has interpretation Above reference range true Inferred relationship Existential restriction modifier 4
Prader-Willi-like syndrome Is a Genetic disease true Inferred relationship Existential restriction modifier

Inbound Relationships Type Active Source Characteristic Refinability Group
6q16 microdeletion syndrome Is a True Prader-Willi-like syndrome Inferred relationship Existential restriction modifier
SIM bHLH transcription factor 1-related Prader-Willi-like syndrome Is a True Prader-Willi-like syndrome Inferred relationship Existential restriction modifier
MAGE family member L2-related Prader-Willi-like syndrome Is a True Prader-Willi-like syndrome Inferred relationship Existential restriction modifier

This concept is not in any reference sets

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