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367004: Clubbing (morphologic abnormality)

SNOMED CT Concept\Body structure\Body structure, altered from its original anatomical structure (morphologic abnormality)\Morphologically abnormal structure\...

\Growth alteration\Proliferation\Clubbing

\Lesion (morphologic abnormality)\Fibrosis AND/OR repair abnormality (morphologic abnormality)\Clubbing

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

Descriptions:

Id Description Lang Type Status Case? Module

1700014 Clubbing en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

768483012 Clubbing (morphologic abnormality) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

2605551000005115 Clubbing da Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Danish module (core metadata concept)

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Clubbing	Is a	Fibrosis AND/OR repair abnormality (morphologic abnormality)	true	Inferred relationship	Some
Clubbing	Is a	Proliferation	true	Inferred relationship	Some

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Kongenitte trommestikfingre/-tæer	Associated morphology	False	Clubbing	Inferred relationship	Some	2
Finger clubbing	Associated morphology	False	Clubbing	Inferred relationship	Some	1
Clubbing of nail	Associated morphology	False	Clubbing	Inferred relationship	Some	1
Clubbing of toes	Associated morphology	False	Clubbing	Inferred relationship	Some	1
Clubbing of toes	Associated morphology	False	Clubbing	Inferred relationship	Some	1
A form of primary hypertrophic osteoarthropathy, a rare hereditary disorder with characteristics of digital clubbing, pachydermia and subperiosteal new bone formation associated with pain, polyarthritis, cutis verticis gyrata, seborrhoea and hyperhidrosis. Three forms have been described: a complete form with pachydermia and periostitis, an incomplete form with evidence of bone abnormalities but lacking pachydermia, and a forme frusta with prominent pachydermia and minimal-to-absent skeletal changes. The disease typically begins during childhood or adolescence and may stabilise after 5-20 years of progression, or progress constantly. Mutations in the HPGD gene (4q33-q34) have been identified. The gene encodes 15-hydroxyprostaglandin dehydrogenase (15-PGDH), the main enzyme of prostaglandin degradation. Inherited as an autosomal recessive trait.	Associated morphology	True	Clubbing	Inferred relationship	Some	1
Clubbing of toes	Associated morphology	False	Clubbing	Inferred relationship	Some	1
Clubbing of toes	Associated morphology	False	Clubbing	Inferred relationship	Some	1
Clubbing of toes	Associated morphology	False	Clubbing	Inferred relationship	Some	2
Clubbing of nails associated with systemic disorder (disorder)	Associated morphology	False	Clubbing	Inferred relationship	Some	1
Clubbing of toes	Associated morphology	False	Clubbing	Inferred relationship	Some	1
Clubbing of toes	Associated morphology	False	Clubbing	Inferred relationship	Some	2
objektivt: trommestikfingre	Associated morphology	False	Clubbing	Inferred relationship	Some	1
Congenital clubnail	Associated morphology	True	Clubbing	Inferred relationship	Some	1
Kongenitte trommestikfingre/-tæer	Associated morphology	False	Clubbing	Inferred relationship	Some	2
objektivt: trommestikfingre	Associated morphology	False	Clubbing	Inferred relationship	Some	1
A form of primary hypertrophic osteoarthropathy, a rare hereditary disorder with characteristics of digital clubbing, pachydermia and subperiosteal new bone formation associated with pain, polyarthritis, cutis verticis gyrata, seborrhoea and hyperhidrosis. Three forms have been described: a complete form with pachydermia and periostitis, an incomplete form with evidence of bone abnormalities but lacking pachydermia, and a forme frusta with prominent pachydermia and minimal-to-absent skeletal changes. The disease typically begins during childhood or adolescence and may stabilise after 5-20 years of progression, or progress constantly. Mutations in the HPGD gene (4q33-q34) have been identified. The gene encodes 15-hydroxyprostaglandin dehydrogenase (15-PGDH), the main enzyme of prostaglandin degradation. Inherited as an autosomal recessive trait.	Associated morphology	False	Clubbing	Inferred relationship	Some	1
Clubbing of nails associated with systemic disorder (disorder)	Associated morphology	True	Clubbing	Inferred relationship	Some	1
Clubbing of nail	Associated morphology	True	Clubbing	Inferred relationship	Some	1
Clubbing of toes	Associated morphology	True	Clubbing	Inferred relationship	Some	1
Finger clubbing	Associated morphology	True	Clubbing	Inferred relationship	Some	1
Kongenitte trommestikfingre/-tæer	Associated morphology	False	Clubbing	Inferred relationship	Some	5
Congenital club finger (disorder)	Associated morphology	False	Clubbing	Inferred relationship	Some	3
Congenital club finger (disorder)	Associated morphology	True	Clubbing	Inferred relationship	Some	1
Hereditary clubbing	Associated morphology	True	Clubbing	Inferred relationship	Some	2

This concept is not in any reference sets

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
1700014	Clubbing	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
768483012	Clubbing (morphologic abnormality)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
2605551000005115	Clubbing	da	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	Danish module (core metadata concept)