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238852002: Fibrotic disorder of skin (disorder)

Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2021. Module: SNOMED CT core

Descriptions:

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Fibrotic disorder of skin	Is a	Degenerative skin disorder	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Fibrotic disorder of skin	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Fibrotic disorder of skin	Associated morphology	Fibrosis (morphologic abnormality)	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Fibrotic disorder of skin	Associated morphology	dégénérescence	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Fibrotic disorder of skin	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Fibrotic disorder of skin	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Fibrotic disorder of skin	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Fibrotic disorder of skin	Is a	Degenerative skin disorder (disorder)	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Fibrotic disorder of skin	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Fibrotic disorder of skin	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Fibrotic disorder of skin	Is a	Fibrosis of the skin (disorder)	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Fibrotic disorder of skin	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Fibrotic disorder of skin	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Fibrotic disorder of skin	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Fibrotic disorder of skin	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Fibrotic disorder of skin	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Fibrotic disorder of skin	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Fibrotic disorder of skin	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Fibrotic disorder of skin	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Fibrotic disorder of skin	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Fibrotic disorder of skin	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Fibrotic disorder of skin	Finding site	Skin and/or subcutaneous tissue structure (body structure)	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Fibrotic disorder of skin	Associated morphology	Degenerative abnormality (morphologic abnormality)	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
A very rare disorder belonging to the heterogeneous group of genetic fibromatoses and with characteristics of progressive joint contractures, skin abnormalities, severe chronic pain and widespread deposition of hyaline material in many tissues such as the skin, skeletal muscle, cardiac muscle, gastrointestinal tract, lymph nodes, spleen, thyroid and adrenal glands. Caused by mutations in anthrax toxin receptor 2 gene (ANTRX2) on chromosome 4q21. Transmitted as an autosomal recessive trait.	Is a	False	Fibrotic disorder of skin	Inferred relationship	Existential restriction modifier (core metadata concept)
Infantile stiff skin syndrome	Is a	False	Fibrotic disorder of skin	Inferred relationship	Existential restriction modifier (core metadata concept)
Juvenile colloid milium (disorder)	Is a	False	Fibrotic disorder of skin	Inferred relationship	Existential restriction modifier (core metadata concept)
Acquired colloid milium	Is a	False	Fibrotic disorder of skin	Inferred relationship	Existential restriction modifier (core metadata concept)
Pseudo-ainhum	Is a	False	Fibrotic disorder of skin	Inferred relationship	Existential restriction modifier (core metadata concept)
Fascial hernia of legs	Is a	False	Fibrotic disorder of skin	Inferred relationship	Existential restriction modifier (core metadata concept)
Ainhum (disorder)	Is a	False	Fibrotic disorder of skin	Inferred relationship	Existential restriction modifier (core metadata concept)
Elastosis perforans serpiginosa	Is a	False	Fibrotic disorder of skin	Inferred relationship	Existential restriction modifier (core metadata concept)
Reactive perforating collagenosis	Is a	False	Fibrotic disorder of skin	Inferred relationship	Existential restriction modifier (core metadata concept)
Fibrosis of the skin (disorder)	Is a	False	Fibrotic disorder of skin	Inferred relationship	Existential restriction modifier (core metadata concept)
Infantile stiff skin syndrome (disorder)	Is a	False	Fibrotic disorder of skin	Inferred relationship	Existential restriction modifier (core metadata concept)
Lethal tight skin contracture syndrome (disorder)	Is a	False	Fibrotic disorder of skin	Inferred relationship	Existential restriction modifier (core metadata concept)

Reference Sets

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

SAME AS association reference set (foundation metadata concept)

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
357973013	Fibrotic disorder of skin	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
627789010	Fibrotic disorder of skin (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
357973013	Fibrotic disorder of skin	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
357973013	Fibrotic disorder of skin	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
627789010	Fibrotic disorder of skin (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
627789010	Fibrotic disorder of skin (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core