39937001: Skin structure (body structure)

SNOMED CT Concept\Body structure\Anatomical or acquired body structure (body structure)\Anatomical structure\...

\An anatomical structure that consists of the maximal set of organ parts so connected to one another that together they constitute a self-contained unit of macroscopic anatomy, distinct both morphologically and functionally from other such units. Together with other organs, an organ constitutes an organ system or a body part. An organ is divisible into organ parts but not organs (examples: femur, biceps, liver, heart, aorta, sciatic nerve, ovary).\Skin structure

\Body tissue structure (body structure)\Structure of soft tissue (body structure)\Skin and/or subcutaneous tissue structure (body structure)\Skin structure

\Body region structure\Skin and/or subcutaneous tissue structure (body structure)\Skin structure

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

Descriptions:

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Skin structure	Is a	Structure of integumentary system (body structure)	false	Inferred relationship	Some
Skin structure	Is a	An anatomical structure that consists of the maximal set of organ parts so connected to one another that together they constitute a self-contained unit of macroscopic anatomy, distinct both morphologically and functionally from other such units. Together with other organs, an organ constitutes an organ system or a body part. An organ is divisible into organ parts but not organs (examples: femur, biceps, liver, heart, aorta, sciatic nerve, ovary).	true	Inferred relationship	Some
Skin structure	Is a	Skin and/or subcutaneous tissue structure (body structure)	true	Inferred relationship	Some
Skin structure	del af	Entire skin AND subcutaneous tissue	false	Additional relationship	Some
Skin structure	Is a	Structure of skin and/or surface epithelium (body structure)	true	Inferred relationship	Some
Skin structure	Is a	Structure of skin and/or skin-associated mucous membrane	true	Inferred relationship	Some

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Keratom	Finding site	False	Skin structure	Inferred relationship	Some	1
adult dermatomyosit	Finding site	False	Skin structure	Inferred relationship	Some	1
Familial partial lipodystrophy	Finding site	False	Skin structure	Inferred relationship	Some	1
Localized pustular psoriasis	Finding site	True	Skin structure	Inferred relationship	Some	1
Bipedicled sensory flap	Procedure site - Indirect (attribute)	False	Skin structure	Inferred relationship	Some	1
Mucoepidermoid carcinoma of skin	Finding site	True	Skin structure	Inferred relationship	Some	1
Lichen planus of lips	Finding site	False	Skin structure	Inferred relationship	Some	1
Lichenoid drug eruption	Finding site	True	Skin structure	Inferred relationship	Some	1
Addison melanoderma	Finding site	True	Skin structure	Inferred relationship	Some	1
Café-au-lait macules with pulmonary stenosis (disorder)	Finding site	False	Skin structure	Inferred relationship	Some	1
Contact dermatitis caused by scabicide	Finding site	False	Skin structure	Inferred relationship	Some	1
Dermatosis due to hair as foreign body (disorder)	Finding site	True	Skin structure	Inferred relationship	Some	1
anden diatermi af hud	Procedure site - Direct (attribute)	False	Skin structure	Inferred relationship	Some	1
Contact urticaria artefacta (disorder)	Finding site	True	Skin structure	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.	Finding site	False	Skin structure	Inferred relationship	Some	2
Lamelløs iktyose OG invagineret trikoreksi-syndrom	Finding site	False	Skin structure	Inferred relationship	Some	1
Metastatic basal cell carcinoma (disorder)	Finding site	True	Skin structure	Inferred relationship	Some	1
Hypermelanosis following phototherapy for neonatal jaundice (disorder)	Finding site	True	Skin structure	Inferred relationship	Some	1
Multiple benign annular creases of extremities	Finding site	False	Skin structure	Inferred relationship	Some	1
Early radiation dermatitis	Finding site	True	Skin structure	Inferred relationship	Some	1
Benign neoplasm of skin with pilar differentiation (disorder)	Finding site	True	Skin structure	Inferred relationship	Some	1
Superficial avulsion wound	Finding site	True	Skin structure	Inferred relationship	Some	1
Chemical-aggravated angioedema-urticaria (disorder)	Finding site	True	Skin structure	Inferred relationship	Some	1
Talgepiteliom	Finding site	False	Skin structure	Inferred relationship	Some	1
Glandulær cyste	Finding site	False	Skin structure	Inferred relationship	Some	1
Nonvenomous insect bite of multiple sites with infection (disorder)	Finding site	False	Skin structure	Inferred relationship	Some	1
Ulcerated angiomatous nevus (disorder)	Finding site	True	Skin structure	Inferred relationship	Some	1
Inflammatorisk hyperkeratotisk dermatose, kronisk	Finding site	False	Skin structure	Inferred relationship	Some	1
Glycerin skin test	Procedure site - Direct (attribute)	True	Skin structure	Inferred relationship	Some	1
Kasabach-Merritt syndrome	Finding site	False	Skin structure	Inferred relationship	Some	1
Basal cell papilloma hyperkeratotic type (disorder)	Finding site	True	Skin structure	Inferred relationship	Some	1
Drug-induced hypomelanosis	Finding site	True	Skin structure	Inferred relationship	Some	1
Radical excision of skin lesion	Procedure site - Direct (attribute)	True	Skin structure	Inferred relationship	Some	2
Erythromelalgia	Finding site	False	Skin structure	Inferred relationship	Some	2
Malignant neoplasm of skin with adnexal differentiation (disorder)	Finding site	True	Skin structure	Inferred relationship	Some	1
excision af morfologisk forandring i hud kontrolleret med frysesnitmikroskopi, ikke klassificeret andetsteds	Procedure site - Direct (attribute)	False	Skin structure	Inferred relationship	Some	1
A rare congenital ectodermal disorder characterized by vascularizing keratitis, hyperkeratotic skin lesions and hearing loss. Patients usually present at birth with generalized erythema and ichthyosiform scaling. The skin manifestations are progressive with erythrokeratoderma characterized by well-demarcated erythematous and keratotic plaques with a verrucous appearance predominantly located on the face, scalp, ears, elbows and knees. Hearing loss is congenital, usually sensorineural and is often profound. Caused by mutations involving the N-terminus and first extracellular loop of the GJB2 gene (13q11-q12), encoding connexin-26. Most of the reported cases are sporadic, but familial cases with autosomal dominant inheritance have been reported.	Finding site	False	Skin structure	Inferred relationship	Some	1
Moist dermatitis of rabbits	Finding site	False	Skin structure	Inferred relationship	Some	1
Infected ulcer of skin	Finding site	True	Skin structure	Inferred relationship	Some	1
Patch/plaque stage mycosis fungoides (disorder)	Finding site	True	Skin structure	Inferred relationship	Some	1
Familial localized cutaneous amyloidosis (disorder)	Finding site	True	Skin structure	Inferred relationship	Some	1
Pigmenteret xeroderma	Finding site	False	Skin structure	Inferred relationship	Some	1
Acneiform drug eruption	Finding site	True	Skin structure	Inferred relationship	Some	1
Skin sinus	Finding site	True	Skin structure	Inferred relationship	Some	1
Other distant skin flap NOS	Procedure site - Indirect (attribute)	False	Skin structure	Inferred relationship	Some	1
Clubbing of toes	Finding site	False	Skin structure	Inferred relationship	Some	3
Deep wound due to human bite (disorder)	Finding site	False	Skin structure	Inferred relationship	Some	1
Irritant contact dermatitis caused by contact with urine and/or faeces	Finding site	False	Skin structure	Inferred relationship	Some	1
Eczema of finger (disorder)	Finding site	False	Skin structure	Inferred relationship	Some	1
Basal cell papilloma clonal type (disorder)	Finding site	True	Skin structure	Inferred relationship	Some	1
Onchodermatitis	Finding site	True	Skin structure	Inferred relationship	Some	1
Dermal nerve sheath myxoma, cellular (disorder)	Finding site	True	Skin structure	Inferred relationship	Some	1
Verruca vulgaris	Finding site	True	Skin structure	Inferred relationship	Some	1
Preoperative shaving of skin	Procedure site - Direct (attribute)	True	Skin structure	Inferred relationship	Some	1
Local subcutaneous pedicle V-Y flap, fasciocutaneous	Procedure site - Indirect (attribute)	False	Skin structure	Inferred relationship	Some	1
Autosomal dominant ichthyosis (disorder)	Finding site	False	Skin structure	Inferred relationship	Some	1
Pinch graft of skin to skin	Procedure site - Direct (attribute)	True	Skin structure	Inferred relationship	Some	1
Pilar sheath acanthoma	Finding site	True	Skin structure	Inferred relationship	Some	1
Drug-aggravated angioedema-urticaria (disorder)	Finding site	True	Skin structure	Inferred relationship	Some	1
Excessive blushing	Finding site	False	Skin structure	Inferred relationship	Some	3
excision af morfologisk forandring i hud på hovedet eller halsen, ikke klassificeret andetsteds	Procedure site - Direct (attribute)	False	Skin structure	Inferred relationship	Some	1
Follicular ichthyosis	Finding site	False	Skin structure	Inferred relationship	Some	1
Stucco keratosis (disorder)	Finding site	True	Skin structure	Inferred relationship	Some	1
Acute urticaria (disorder)	Finding site	True	Skin structure	Inferred relationship	Some	1
Local advancement flap, random pattern	Procedure site - Indirect (attribute)	False	Skin structure	Inferred relationship	Some	1
Sézary's disease NOS	Finding site	False	Skin structure	Inferred relationship	Some	1
Application of dressing for second degree burn	Procedure site - Indirect (attribute)	False	Skin structure	Inferred relationship	Some	1
Excision of pressure injury of greater femoral trochanteric region with flap reconstruction using bipedicle flap	Procedure site - Direct (attribute)	False	Skin structure	Inferred relationship	Some	2
Chronic lichenified atopic dermatitis	Finding site	True	Skin structure	Inferred relationship	Some	1
Localized vitiligo (disorder)	Finding site	True	Skin structure	Inferred relationship	Some	1
[X]Melanoma and other malignant neoplasms of skin	Finding site	False	Skin structure	Inferred relationship	Some	1
Examination of skin	Procedure site - Direct (attribute)	True	Skin structure	Inferred relationship	Some	1
Urticarial reaction to blood product (disorder)	Finding site	True	Skin structure	Inferred relationship	Some	1
Kontaktdermatit forårsaget af æg	Finding site	False	Skin structure	Inferred relationship	Some	1
Acute-on-chronic vesicular eczema of hands and feet	Finding site	False	Skin structure	Inferred relationship	Some	1
Prurigopapel	Finding site	False	Skin structure	Inferred relationship	Some	1
Contact dermatitis caused by urine (disorder)	Finding site	False	Skin structure	Inferred relationship	Some	2
Punctate palmoplantar keratoderma (disorder)	Finding site	False	Skin structure	Inferred relationship	Some	1
A rare type of keratinopathic ichthyosis characterised by the presence of severe hyperkeratotic lesions and palmoplantar keratoderma. The skin is usually normal at birth. The disease starts in early childhood with severe hyperkeratosis of yellow-brown or grey colour, and of spiky, cobblestone-like (hystrix) or verrucous appearance. Contrary to other keratinopathic ichthyoses, no skin fragility/blister formation or erythroderma is present. The disease results from heterozygous frameshift mutation in a section of the KRT1 gene encoding keratin 1 (K1). These mutations lead to an abnormal supramolecular organisation of keratin intermediate filaments and may be related to defects in cytoplasmic trafficking and integrity of cellular structures such as organelles and nucleus. Transmission is autosomal dominant but some sporadic cases have been reported.	Finding site	False	Skin structure	Inferred relationship	Some	1
Odontotrichomelic syndrome	Finding site	False	Skin structure	Inferred relationship	Some	2
Lipoatrophy (disorder)	Finding site	False	Skin structure	Inferred relationship	Some	1
[X]Superficial frostbite of other and unspecified sites	Finding site	False	Skin structure	Inferred relationship	Some	1
Syphilitic leukoderma	Finding site	True	Skin structure	Inferred relationship	Some	1
Apocrine adenocarcinoma of skin (disorder)	Finding site	True	Skin structure	Inferred relationship	Some	1
Phototoxic reaction to dye	Finding site	True	Skin structure	Inferred relationship	Some	1
Skin hypopigmented	Finding site	True	Skin structure	Inferred relationship	Some	1
Corns and callosities NOS	Finding site	False	Skin structure	Inferred relationship	Some	1
Delayed hypersensitivity skin test for coccidiodin	Procedure site - Direct (attribute)	True	Skin structure	Inferred relationship	Some	1
Local rotation flap, axial pattern	Procedure site - Indirect (attribute)	False	Skin structure	Inferred relationship	Some	1
Hajdu-Cheney syndrome	Finding site	False	Skin structure	Inferred relationship	Some	2
Superficial frostbite (disorder)	Finding site	True	Skin structure	Inferred relationship	Some	1
Sézary's disease of unspecified site	Finding site	False	Skin structure	Inferred relationship	Some	1
Ultraviolet A light therapy to skin (procedure)	Procedure site - Direct (attribute)	True	Skin structure	Inferred relationship	Some	1
Psoriasis unspecified	Finding site	False	Skin structure	Inferred relationship	Some
Generalized eczema (disorder)	Finding site	True	Skin structure	Inferred relationship	Some	1
Curry-Hall syndrome	Finding site	False	Skin structure	Inferred relationship	Some	1
Lentigo simplex (disorder)	Finding site	False	Skin structure	Inferred relationship	Some	1
Acneiform eruption (disorder)	Finding site	True	Skin structure	Inferred relationship	Some	1
Benign neoplasm of sweat gland	Finding site	False	Skin structure	Inferred relationship	Some	2
Symptomatic dermographism (disorder)	Finding site	True	Skin structure	Inferred relationship	Some	1
Other specified punch biopsy of skin	Procedure site - Direct (attribute)	False	Skin structure	Inferred relationship	Some	1

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Reference Sets

Anatomy structure and entire association reference set (foundation metadata concept)

Anatomy structure and part association reference set (foundation metadata concept)

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Id	Description	Lang	Type	Status	Case?	Module
66527011	Skin	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
66528018	Skin, NOS	en	Synonym (core metadata concept)	Inactive	Only initial character case insensitive (core metadata concept)	SNOMED CT core
66529014	Integument	en	Synonym (core metadata concept)	Inactive	Only initial character case insensitive (core metadata concept)	SNOMED CT core
492326013	Skin structure	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
776485012	Skin structure (body structure)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
2677331000005119	Hud	da	Synonym (core metadata concept)	Inactive	Entire term case insensitive (core metadata concept)	Danish module (core metadata concept)
4249211000005115	hudstruktur	da	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	Danish module (core metadata concept)