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39937001: Skin structure (body structure)

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
66527011 Skin en Synonym (core metadata concept) Active Entire term 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
274021000077119 structure de la peau fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
922751000172111 peau fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
946531000172113 cutis fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

1747 descendants. Search Descendants:

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 partie de 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 Region consisting of all body skin and directly related mucosa but excluding mucosa within the body such as the mucous membrane of the urinary bladder. true Inferred relationship Some
Inbound Relationships Type Active Source Characteristic Refinability Group
Neutrophilic eccrine hidradenitis Finding site True Skin structure Inferred relationship Some 3
Malignant pyoderma Finding site True Skin structure Inferred relationship Some 3
Abscess of skin during pregnancy (disorder) Finding site True Skin structure Inferred relationship Some 1
Open wound of skin (disorder) Finding site True Skin structure Inferred relationship Some 1
Diascopy procedure Procedure site - Direct (attribute) True Skin structure Inferred relationship Some 1
Neonatal skin maturity optical reader (physical object) This attribute represents the site where the device is intended to reside in or on the body. True Skin structure Inferred relationship Some
Keratinocytic epidermal carcinoma of skin (disorder) Finding site True Skin structure Inferred relationship Some 1
Neonatal infection of skin caused by Candida Finding site True Skin structure Inferred relationship Some 1
A rare inherited connective tissue disorder characterised by skin hyperextensibility, widened atrophic scars and generalised joint hypermobility. The disease is caused by heterozygous mutation in the collagen alpha-2(V) gene (COL5A2) on chromosome 2q31. Finding site True Skin structure Inferred relationship Some 2
Eruption of skin caused by Salmonella (disorder) Finding site True Skin structure Inferred relationship Some 1
Eruption of skin caused by Salmonella enterica enterica serovar Typhi (disorder) Finding site True Skin structure Inferred relationship Some 1
Electrodesiccation of lesion of skin Procedure site - Direct (attribute) True Skin structure Inferred relationship Some 1
Eruption of skin caused by Salmonella Paratyphi Finding site True Skin structure Inferred relationship Some 1
Eruption of skin caused by Salmonella Paratyphi A (disorder) Finding site True Skin structure Inferred relationship Some 1
Eruption of skin caused by Salmonella Paratyphi B (disorder) Finding site True Skin structure Inferred relationship Some 1
Eruption of skin caused by Salmonella Paratyphi C Finding site True Skin structure Inferred relationship Some 1
Photo-induced Stevens-Johnson syndrome (disorder) Finding site True Skin structure Inferred relationship Some 1
Photo-induced Stevens-Johnson syndrome (disorder) Finding site True Skin structure Inferred relationship Some 3
Photo-induced Stevens-Johnson syndrome (disorder) Finding site True Skin structure Inferred relationship Some 4
Destruction of multiple fibroepithelial polyps using electrical energy (procedure) Procedure site - Direct (attribute) True Skin structure Inferred relationship Some 1
Cauterization of fibroepithelial polyp using electrical energy (procedure) Procedure site - Direct (attribute) True Skin structure Inferred relationship Some 1
Rosacea, erythematous telangiectatic type (disorder) Finding site True Skin structure Inferred relationship Some 2
Sézary syndrome of inguinal lymph nodes (disorder) Finding site True Skin structure Inferred relationship Some 1
Mycosis fungoides of axillary lymph nodes (disorder) Finding site True Skin structure Inferred relationship Some 1
Congenital cutaneous mastocytosis Finding site True Skin structure Inferred relationship Some 2
Phymatous rosacea (disorder) Finding site True Skin structure Inferred relationship Some 1
Lupus panniculitis Finding site True Skin structure Inferred relationship Some 3
Skin test Procedure site True Skin structure Inferred relationship Some 1
Kveim test skin biopsy Procedure site True Skin structure Inferred relationship Some 3
Injection of Kveim antigen into skin Procedure site True Skin structure Inferred relationship Some 2
Dermographia test Procedure site True Skin structure Inferred relationship Some 2
Puncture test Procedure site True Skin structure Inferred relationship Some 2
Scratch test Procedure site - Direct (attribute) True Skin structure Inferred relationship Some 1
Prausnitz-Kustner test Procedure site True Skin structure Inferred relationship Some 2
Skin test for leprosy Procedure site True Skin structure Inferred relationship Some 2
Lepromin H skin test Procedure site False Skin structure Inferred relationship Some 2
Lepromin A skin test Procedure site False Skin structure Inferred relationship Some 2
Mitsuda reaction to lepromin Procedure site True Skin structure Inferred relationship Some 1
Curette test of skin Procedure site True Skin structure Inferred relationship Some 2
Kveim test Procedure site True Skin structure Inferred relationship Some 2
Skin testing: metals (procedure) Procedure site False Skin structure Inferred relationship Some 2
Intradermal test of type 1 hypersensitivity (procedure) Procedure site False Skin structure Inferred relationship Some 1
Subcutaneous test of type 1 hypersensitivity Procedure site False Skin structure Inferred relationship Some 1
Contact sensitivity test Procedure site True Skin structure Inferred relationship Some 2
Dinitrochlorobenzene contact sensitivity test Procedure site True Skin structure Inferred relationship Some 1
Hypersensitivity skin testing Procedure site True Skin structure Inferred relationship Some 1
Type 1 hypersensitivity skin test Procedure site False Skin structure Inferred relationship Some 2
Superficial contusion of skin (disorder) Finding site True Skin structure Inferred relationship Some 1
Plaque-like dermatofibrosarcoma protuberans (disorder) Finding site True Skin structure Inferred relationship Some 1
Mycoplasma pneumoniae induced rash and mucositis (disorder) Finding site True Skin structure Inferred relationship Some 2
A combination of congenital hyperpigmented and hypopigmented skin lesions coexisting in the same individual. Finding site True Skin structure Inferred relationship Some 1
A combination of congenital hyperpigmented and hypopigmented skin lesions coexisting in the same individual. Finding site True Skin structure Inferred relationship Some 2
Excision of pilonidal sinus and closure with skin flap (procedure) Procedure site - Direct (attribute) True Skin structure Inferred relationship Some 2
Excision of pilonidal sinus and grafting of skin (procedure) Procedure site - Direct (attribute) True Skin structure Inferred relationship Some 2
Atypical melanocytic hyperplasia of skin (disorder) Finding site True Skin structure Inferred relationship Some 1
A rare developmental defect during embryogenesis characterised by unilateral inflammatory and scaling skin lesions with ipsilateral visceral and limb anomalies. Finding site True Skin structure Inferred relationship Some 1
Atypical blue nevus of skin (disorder) Finding site True Skin structure Inferred relationship Some 1
Introduction into skin (procedure) Procedure site - Indirect (attribute) True Skin structure Inferred relationship Some 1
Replacement of tissue expander of skin with permanent prosthesis Procedure site - Indirect (attribute) True Skin structure Inferred relationship Some 3
PENS syndrome is a rare, genetic, neurocutaneous syndrome characterized by the presence of randomly distributed, small, white to yellowish, multiple, rounded or irregular polycyclically-shaped, epidermal keratotic papules and plaques of gem-like appearance with a rough surface, typically located on the trunk and proximal limbs, associated with variable neurological abnormalities, including psychomotor delay, epilepsy, speech and language impairment and attention deficit-hyperactivity disorder. Clumsiness, dyslexia and ophthalmological abnormalities have also been reported. Finding site True Skin structure Inferred relationship Some 4
Neurocutaneous melanosis Finding site True Skin structure Inferred relationship Some 2
Herpes zoster dermatitis (disorder) Finding site True Skin structure Inferred relationship Some 3
A rare genetic neurometabolic disease with characteristics of prenatal and postnatal growth retardation, hypotonia, failure to thrive, large and late-closing fontanel, development delay, cutis laxa, joint laxity, progeroid appearance and dysmorphic facial features. In addition, corneal opacities, cataracts, myopia, seizures, hyperreflexia and athetoid movements have also been associated. Finding site True Skin structure Inferred relationship Some 4
Pyrroline-5-carboxylate reductase 1 related de Barsy syndrome Finding site True Skin structure Inferred relationship Some 4
An association reported in a single kindred characterized by the variable presence of the following features: anetodermia (macular atrophy of the skin), multiple exostoses, and brachydactyly type E. There have been no further descriptions in the literature since 1985. Finding site True Skin structure Inferred relationship Some 3
Incision and drainage of pustule (procedure) Procedure site - Direct (attribute) True Skin structure Inferred relationship Some 1
Incision and drainage of pustule (procedure) Procedure site - Indirect (attribute) True Skin structure Inferred relationship Some 2
Incision and drainage of cyst of skin Procedure site - Direct (attribute) True Skin structure Inferred relationship Some 1
Incision and drainage of cyst of skin Procedure site - Indirect (attribute) True Skin structure Inferred relationship Some 2
Exacerbation of psoriasis (disorder) Finding site True Skin structure Inferred relationship Some 1
Eruptive xanthoma Finding site True Skin structure Inferred relationship Some 2
Diffuse normolipemic plane xanthomatosis (disorder) Finding site True Skin structure Inferred relationship Some 2
Application of cosmetic camouflage (procedure) Procedure site - Direct (attribute) True Skin structure Inferred relationship Some 1
Neonatal inflammatory skin and bowel disease is a rare, life-threatening, autoinflammatory syndrome with immune deficiency disorder characterized by early-onset, life-long inflammation, affecting the skin and bowel, associated with recurrent infections. Patients present perioral and perianal psoriasiform erythema and papular eruption with pustules, failure to thrive associated with chronic malabsorptive diarrhea, intercurrent gastrointestinal infections and feeding troubles, as well as absent, short or broken hair and trichomegaly. Recurrent cutaneous and pulmonary infections lead to recurrent blepharitis, otitis externa and bronchiolitis. Finding site True Skin structure Inferred relationship Some 1
Granulomatous slack skin disease Finding site True Skin structure Inferred relationship Some 3
Linear atrophoderma of Moulin (disorder) Finding site True Skin structure Inferred relationship Some 2
A rare, acquired, dermis elastic tissue disorder with decreased elastic tissue characterized by multiple, asymptomatic, well demarcated, flat, hypopigmented atrophic macular skin lesions distributed over upper trunk and proximal upper limbs. Histopathological examination reveals atrophic epidermis with decreased basal pigmentation, perivascular mononuclear infiltration in the upper dermis, and disorganized, hyalinized, coarse collagen bundles, and variable loss of elastic fibers in the dermis. Finding site True Skin structure Inferred relationship Some 3
Excision of lymphedematous tissue and split thickness graft of skin (procedure) Procedure site - Direct (attribute) True Skin structure Inferred relationship Some 2
Oculocutaneous albinism type 8 (disorder) Finding site True Skin structure Inferred relationship Some 1
Biopsy of skin of fetus (procedure) Procedure site - Direct (attribute) True Skin structure Inferred relationship Some 1
Infantile pustular psoriasis Finding site True Skin structure Inferred relationship Some 4
A rare, genetic, autoinflammatory syndrome with immune deficiency disease characterized by recurrent and severe flares of generalized pustular psoriasis associated with high fever, asthenia, and systemic inflammation, due to IL36R antagonist deficiency. Psoriatic nail changes (e.g. pitting and onychomadesis) and ichthyosis may occasionally be associated. Finding site True Skin structure Inferred relationship Some 5
Pityriasis rubra pilaris Finding site True Skin structure Inferred relationship Some 4
Pityriasis rubra (Hebra) Finding site True Skin structure Inferred relationship Some 4
Nail dystrophy due to pityriasis rubra pilaris (disorder) Finding site True Skin structure Inferred relationship Some 6
Pityriasis rubra pilaris due to human immunodeficiency virus infection (disorder) Finding site True Skin structure Inferred relationship Some 5
Therapeutic paraffin bath Procedure site - Indirect (attribute) True Skin structure Inferred relationship Some 1
A rare mosaic form of Legius syndrome with findings typical of Legius syndrome, namely multiple cafe-au-lait macules (CALMs) with or without axillary or inguinal freckling. Mosaic form is caused by postzygotic pathogenic variants in SPRED1 gene. In mosaic Legius syndrome the allelic/tissue distribution of the pathogenic SPRED1-variant clearly suggests mosaicism and/or the distribution of CALMs is segmental. The phenotype can be milder than in Legius syndrome. Finding site True Skin structure Inferred relationship Some 1
Infrared photocoagulation of lesion of skin Procedure site - Direct (attribute) True Skin structure Inferred relationship Some 1
Carcinomatous transformation of chromoblastomycosis Finding site True Skin structure Inferred relationship Some 2
A rare hypersensitivity reaction with characteristics of the rapid development of numerous, nonfollicular, sterile, pinhead-sized pustules on an erythematous base, predominantly occurring on the trunk, intertriginous and flexural areas, with rare, mostly oral, mucosal involvement. Fever, peripheral blood leukocytosis, and mild eosinophilia are accompanying features. Systemic involvement, with hepatic, renal or pulmonary dysfunction, occasionally occurs. Onset usually occurs 1-12 days after administration of the causal medication and is most frequently associated with beta‐lactam antibiotics, macrolides (including pristinamycin and clindamycin), diltiazem, terbinafine, (hydroxy‐)chloroquine but many other medications have also been implicated. Histology reveals spongiform, subcorneal and/or intraepidermal, pustules but this pattern is not specific (same in pustular psoriasis). Finding site True Skin structure Inferred relationship Some 1
Painting of perineal warts (procedure) Procedure site - Direct (attribute) True Skin structure Inferred relationship Some 2
Injection of corticosteroid and/or corticosteroid derivative into keloid (procedure) Procedure site - Indirect (attribute) True Skin structure Inferred relationship Some 1
A rare mosaic form of neurofibromatosis type 1 (NF1) characterised by findings typical of NF1, namely multiple cafe-au-lait macules (CALMs), cutaneous neurofibromas, skinfold freckling/lentiginous macules, iris Lisch nodules and tumours of the nervous system. Mosaic form is caused by postzygotic pathogenic variants in NF1-gene. In mosaic NF1 the allelic/tissue distribution of the pathogenic NF1-variant clearly suggests mosaicism and/or the distribution of CALMs and cutaneous neurofibromas is segmental. The phenotype can be milder than in NF1. Finding site True Skin structure Inferred relationship Some 2
A rare mosaic form of NF2-related schwannomatosis characterised by findings typical of NF2-related schwannomatosis, namely development of multiple benign nerve sheath tumours, particularly affecting the vestibular nerve. Mosaic form is caused by postzygotic pathogenic variants in NF2. In mosaic NF2-related schwannomatosis the allelic/tissue distribution of the pathogenic NF2 variant clearly suggests mosaicism. The phenotype can be milder than in NF2-related schwannomatosis. Finding site True Skin structure Inferred relationship Some 3
Marsupialization of skin lesion Procedure site - Direct (attribute) True Skin structure Inferred relationship Some 1
A form of cutaneous mastocytosis (CM) characterised by the presence of multiple hyperpigmented macules, papules or nodules associated with abnormal accumulation of mast cells in the skin. Most patients present in infancy or childhood, but onset may also occur in adulthood. Mutations in the KIT gene (4q11-q12) have been identified however this mutation is rare in the paediatric population and the aetiology and pathogenesis in these cases remains to be determined. The disease generally occurs sporadically but rare familial cases have been reported. Finding site True Skin structure Inferred relationship Some 2
A form of cutaneous mastocytosis (CM) characterised by the presence of multiple hyperpigmented macules, papules or nodules associated with abnormal accumulation of mast cells in the skin. Most patients present in infancy or childhood, but onset may also occur in adulthood. Mutations in the KIT gene (4q11-q12) have been identified however this mutation is rare in the paediatric population and the aetiology and pathogenesis in these cases remains to be determined. The disease generally occurs sporadically but rare familial cases have been reported. Finding site True Skin structure Inferred relationship Some 5
Telangiectasia macularis eruptiva perstans Finding site True Skin structure Inferred relationship Some 5
Contact dermatitis caused by medication (disorder) Finding site True Skin structure Inferred relationship Some 1
Segmental pigmentation disorder Finding site True 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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