FHIR © HL7.org | Server Home | FHIR Server FHIR Server 3.7.10 | FHIR Version n/a User: [n/a]

89392001: Prader-Willi syndrome (disorder)

SNOMED CT Concept\Clinical finding\...

\Finding of head and neck region\Head finding\...

\Finding of brain\Disorder of brain\Limbic disorder\Disorder of hypothalamus\Disorder of pituitary gland\...

\Hypopituitarism\Hypogonadotropic hypogonadism\Congenital hypogonadotropic hypogonadism\Prader-Willi syndrome

\Disorder of anterior pituitary\Hypogonadotropic hypogonadism\Congenital hypogonadotropic hypogonadism\Prader-Willi syndrome

\Disorder of head\Disorder of brain\Limbic disorder\Disorder of hypothalamus\Disorder of pituitary gland\...

\Hypopituitarism\Hypogonadotropic hypogonadism\Congenital hypogonadotropic hypogonadism\Prader-Willi syndrome

\Disorder of anterior pituitary\Hypogonadotropic hypogonadism\Congenital hypogonadotropic hypogonadism\Prader-Willi syndrome

\Disease\Genetic disease\Prader-Willi syndrome
\Disease\Disorder of embryonic structure\Disorder of hypothalamus\Disorder of pituitary gland\Hypopituitarism\Hypogonadotropic hypogonadism\Congenital hypogonadotropic hypogonadism\Prader-Willi syndrome
\Disease\Disorder of embryonic structure\Disorder of hypothalamus\Disorder of pituitary gland\Disorder of anterior pituitary\Hypogonadotropic hypogonadism\Congenital hypogonadotropic hypogonadism\Prader-Willi syndrome
\Disease\Disorder of body system\Disorder of endocrine system\Disorder of pituitary gland\Hypopituitarism\Hypogonadotropic hypogonadism\Congenital hypogonadotropic hypogonadism\Prader-Willi syndrome
\Disease\Disorder of body system\Disorder of endocrine system\Disorder of pituitary gland\Disorder of anterior pituitary\Hypogonadotropic hypogonadism\Congenital hypogonadotropic hypogonadism\Prader-Willi syndrome
\Disease\Disorder of body system\Disorder of endocrine system\Disorder of endocrine gonad\Hypogonadism\Hypogonadotropic hypogonadism\Congenital hypogonadotropic hypogonadism\Prader-Willi syndrome
\Disease\Disorder of body system\Disorder of nervous system\Disorder of the central nervous system\Disorder of brain\Limbic disorder\Disorder of hypothalamus\Disorder of pituitary gland\Hypopituitarism\Hypogonadotropic hypogonadism\Congenital hypogonadotropic hypogonadism\Prader-Willi syndrome
\Disease\Disorder of body system\Disorder of nervous system\Disorder of the central nervous system\Disorder of brain\Limbic disorder\Disorder of hypothalamus\Disorder of pituitary gland\Disorder of anterior pituitary\Hypogonadotropic hypogonadism\Congenital hypogonadotropic hypogonadism\Prader-Willi syndrome
\Disease\Disorder of body system\Disorder of the genitourinary system\Disorder of reproductive system\Disorder of endocrine gonad\Hypogonadism\Hypogonadotropic hypogonadism\Congenital hypogonadotropic hypogonadism\Prader-Willi syndrome
\Disease\Disorder of trunk\Disorder of abdominopelvic segment of trunk\Disorder of the genitourinary system\Disorder of reproductive system\Disorder of endocrine gonad\Hypogonadism\Hypogonadotropic hypogonadism\Congenital hypogonadotropic hypogonadism\Prader-Willi syndrome
\Disease\Disorder of head\Disorder of brain\Limbic disorder\Disorder of hypothalamus\Disorder of pituitary gland\Hypopituitarism\Hypogonadotropic hypogonadism\Congenital hypogonadotropic hypogonadism\Prader-Willi syndrome
\Disease\Disorder of head\Disorder of brain\Limbic disorder\Disorder of hypothalamus\Disorder of pituitary gland\Disorder of anterior pituitary\Hypogonadotropic hypogonadism\Congenital hypogonadotropic hypogonadism\Prader-Willi syndrome
\Disease\Congenital disease\Congenital hypogonadotropic hypogonadism\Prader-Willi syndrome
\Disease\Congenital disease\Congenital malformation\Congenital malformation syndrome\Multiple system malformation syndrome\Prader-Willi syndrome
\Disease\Developmental disorder\Neurodevelopmental disorder\Prader-Willi syndrome
\Disease\Developmental disorder\Congenital malformation\Congenital malformation syndrome\Multiple system malformation syndrome\Prader-Willi syndrome

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module

148214012 Prader-Willi syndrome en Synonym Active Entire term case sensitive SNOMED CT core module

832276019 Prader-Willi syndrome (disorder) en Fully specified name Active Entire term case sensitive SNOMED CT core module

3793256012 Prader Labhart Willi syndrome en Synonym Active Entire term case sensitive SNOMED CT core module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Prader-Willi syndrome	Is a	Anomaly of chromosome pair 15	false	Inferred relationship	Existential restriction modifier
Prader-Willi syndrome	Is a	Multiple malformation syndrome with unusual brain and/or neuromuscular findings	false	Inferred relationship	Existential restriction modifier
Prader-Willi syndrome	Finding site	Chromosome pair 15	false	Inferred relationship	Existential restriction modifier	1
Prader-Willi syndrome	Finding site	Sex chromosome	false	Inferred relationship	Existential restriction modifier
Prader-Willi syndrome	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier
Prader-Willi syndrome	Finding site	Brain structure	false	Inferred relationship	Existential restriction modifier	2
Prader-Willi syndrome	Associated morphology	Alteration of chromosome structure	false	Inferred relationship	Existential restriction modifier
Prader-Willi syndrome	Associated morphology	Congenital malformation	false	Inferred relationship	Existential restriction modifier
Prader-Willi syndrome	Associated morphology	Congenital anomaly	false	Inferred relationship	Existential restriction modifier	1
Prader-Willi syndrome	Associated morphology	Congenital anomaly	false	Inferred relationship	Existential restriction modifier	1
Prader-Willi syndrome	Finding site	Chromosome pair 15	false	Inferred relationship	Existential restriction modifier	1
Prader-Willi syndrome	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier	1
Prader-Willi syndrome	Finding site	Chromosome pair 15	false	Inferred relationship	Existential restriction modifier	1
Prader-Willi syndrome	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier	2
Prader-Willi syndrome	Associated morphology	Cellular AND/OR subcellular abnormality	false	Inferred relationship	Existential restriction modifier	1
Prader-Willi syndrome	Associated morphology	Developmental anomaly	false	Inferred relationship	Existential restriction modifier	2
Prader-Willi syndrome	Associated morphology	Morphologically abnormal structure	true	Inferred relationship	Existential restriction modifier	2
Prader-Willi syndrome	Pathological process	Pathological developmental process	true	Inferred relationship	Existential restriction modifier	2
Prader-Willi syndrome	Is a	Congenital hypogonadotropic hypogonadism	true	Inferred relationship	Existential restriction modifier
Prader-Willi syndrome	Is a	Genetic disease	true	Inferred relationship	Existential restriction modifier
Prader-Willi syndrome	Is a	Neurodevelopmental disorder	true	Inferred relationship	Existential restriction modifier
Prader-Willi syndrome	Is a	Multiple system malformation syndrome	true	Inferred relationship	Existential restriction modifier
Prader-Willi syndrome	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier	3
Prader-Willi syndrome	Finding site	Structure of pars distalis of pituitary	true	Inferred relationship	Existential restriction modifier	3
Prader-Willi syndrome	Finding site	Gonadal endocrine structure	true	Inferred relationship	Existential restriction modifier	1

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Family history of Prader-Willi syndrome	Associated finding	True	Prader-Willi syndrome	Inferred relationship	Existential restriction modifier	1

This concept is not in any reference sets

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
148214012	Prader-Willi syndrome	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module
832276019	Prader-Willi syndrome (disorder)	en	Fully specified name	Active	Entire term case sensitive	SNOMED CT core module
3793256012	Prader Labhart Willi syndrome	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module