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2298005: Goltz syndrome (disorder)

Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2020. Module: SNOMED CT core

Descriptions:

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Goltz syndrome	Is a	Congenital hamartosis	false	Inferred relationship	Some
Goltz syndrome	Is a	Congenital anomaly of face	false	Inferred relationship	Some
Goltz syndrome	Is a	Nevi, hamartomas and developmental anomalies	false	Inferred relationship	Some
Goltz syndrome	Is a	Disorder of skin AND/OR subcutaneous tissue of head (disorder)	false	Inferred relationship	Some
Goltz syndrome	Is a	Congenital anomaly of integument	false	Inferred relationship	Some
Goltz syndrome	Finding site	Skin of part of face	false	Inferred relationship	Some
Goltz syndrome	Occurrence	Congenital	false	Inferred relationship	Some
Goltz syndrome	Finding site	Dermis structure (body structure)	false	Inferred relationship	Some	1
Goltz syndrome	Associated morphology	Hypoplasia	false	Inferred relationship	Some	1
Goltz syndrome	Is a	Congenital anomaly of skin	false	Inferred relationship	Some
Goltz syndrome	Is a	Skin lesion	false	Inferred relationship	Some
Goltz syndrome	Associated morphology	anomalie congénitale	false	Inferred relationship	Some	2
Goltz syndrome	Associated morphology	Hamartoma	false	Inferred relationship	Some
Goltz syndrome	Finding site	Skin structure	false	Inferred relationship	Some	2
Goltz syndrome	Associated morphology	anomalie congénitale	false	Inferred relationship	Some	2
Goltz syndrome	Finding site	Skin structure	false	Inferred relationship	Some	2
Goltz syndrome	Associated morphology	Hypoplasia	false	Inferred relationship	Some	1
Goltz syndrome	Finding site	Dermis structure (body structure)	false	Inferred relationship	Some	1
Goltz syndrome	Occurrence	Congenital	false	Inferred relationship	Some	3
Goltz syndrome	Is a	Congenital hamartoma (disorder)	false	Inferred relationship	Some
Goltz syndrome	Occurrence	Congenital	false	Inferred relationship	Some	4
Goltz syndrome	Associated morphology	Hamartoma	false	Inferred relationship	Some	4
Goltz syndrome	Associated morphology	Hypoplasia	false	Inferred relationship	Some	3
Goltz syndrome	Finding site	Dermis structure (body structure)	false	Inferred relationship	Some	3
Goltz syndrome	Occurrence	Congenital	false	Inferred relationship	Some	2
Goltz syndrome	Associated morphology	Hamartoma	false	Inferred relationship	Some	2
Goltz syndrome	Pathological process (attribute)	Pathological developmental process	false	Inferred relationship	Some	2
Goltz syndrome	Pathological process (attribute)	Pathological developmental process	false	Inferred relationship	Some	1
Goltz syndrome	Occurrence	Congenital	false	Inferred relationship	Some	1

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

Reference Sets

Concept inactivation indicator reference set

SAME AS association reference set (foundation metadata concept)

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Id	Description	Lang	Type	Status	Case?	Module
4954016	Goltz syndrome	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
4955015	Focal dermal hypoplasia syndrome	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
4956019	Goltz-Gorlin syndrome	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
752449013	Goltz syndrome (disorder)	en	Fully specified name	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
3035263018	Goltz-Gorlin (dermal hypoplasia) syndrome	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
3036043010	Goltz Gorlin syndrome	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core