8632008: Schwartz syndrome (disorder)

Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2017. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

15240011 Schwartz syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core

828560014 Schwartz syndrome (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core

15240011 Schwartz syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core

828560014 Schwartz syndrome (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core

828560014 Schwartz syndrome (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Schwartz syndrome	Is a	Congenital anomaly of endocrine gland	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Schwartz syndrome	Is a	Syndrome of inappropriate vasopressin secretion	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Schwartz syndrome	Is a	Multiple malformation syndrome with unusual brain and/or neuromuscular findings	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Schwartz syndrome	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Schwartz syndrome	Finding site	Entire endocrine gonad (body structure)	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Schwartz syndrome	Finding site	Pars nervosa of pituitary gland	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Schwartz syndrome	Is a	Congenital anomaly of pituitary gland	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Schwartz syndrome	Associated morphology	Congenital malformation	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Schwartz syndrome	Finding site	Brain structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Schwartz syndrome	Finding site	Neurohypophysis structure (body structure)	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Schwartz syndrome	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Schwartz syndrome	Associated morphology	anomalie du développement	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

Reference Sets

Concept inactivation indicator attribute value reference set (foundation metadata concept)

POSSIBLY EQUIVALENT TO association reference set