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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
purpura thrombopénique idiopathique Finding site False Skin structure Inferred relationship Some 3
Infection-associated purpura Finding site True Skin structure Inferred relationship Some 1
Cryoglobulinemic purpura Finding site True Skin structure Inferred relationship Some 1
Posttransfusion purpura Finding site False Skin structure Inferred relationship Some 2
Purpura rheumatica Finding site False Skin structure Inferred relationship Some 1
Stellate pseudoscar in senile purpura (disorder) Finding site True Skin structure Inferred relationship Some 1
Acquired thrombotic thrombocytopenic purpura (disorder) Finding site False Skin structure Inferred relationship Some 5
purpura Finding site False Skin structure Inferred relationship Some 1
Purpura simplex Finding site True Skin structure Inferred relationship Some 1
Senile purpura Finding site True Skin structure Inferred relationship Some 1
Immunoglobulin A vasculitis Finding site False Skin structure Inferred relationship Some 2
Benign primary hypergammaglobulinemic purpura Finding site True Skin structure Inferred relationship Some 1
Traumatic petechiae Finding site True Skin structure Inferred relationship Some 1
dermatite ocra di Favre Finding site False Skin structure Inferred relationship Some 1
Steroid purpura Finding site True Skin structure Inferred relationship Some 1
Stasis purpura Finding site True Skin structure Inferred relationship Some 1
Thrombotic thrombocytopenic purpura Finding site True Skin structure Inferred relationship Some 5
Non-thrombocytopenic purpura Finding site True Skin structure Inferred relationship Some 1
Primary non-thrombocytopenic purpura Finding site True Skin structure Inferred relationship Some 1
Thrombocytopenic purpura associated with metabolic disorder (disorder) Finding site True Skin structure Inferred relationship Some 2
Purpuric disorder (disorder) Finding site True Skin structure Inferred relationship Some 1
Metabolic purpura Finding site True Skin structure Inferred relationship Some 1
On examination - mouth - purpuric spots Finding site False Skin structure Inferred relationship Some 4
Skin disorder due to phototherapy (disorder) Finding site True Skin structure Inferred relationship Some 1
PUVA therapy-associated basal cell carcinoma Finding site False Skin structure Inferred relationship Some 2
Syphilitic leukoderma Finding site False Skin structure Inferred relationship Some 2
Pseudoporphyria due to PUVA therapy Finding site True Skin structure Inferred relationship Some 1
PUVA phototherapy burn Finding site False Skin structure Inferred relationship Some 1
Phototherapy skin rash Finding site False Skin structure Inferred relationship Some 2
PUVA therapy-associated malignant melanoma Finding site False Skin structure Inferred relationship Some 2
Psoralen and long-wave ultraviolet radiation (PUVA) keratosis Finding site True Skin structure Inferred relationship Some 1
Burn of skin due to and following ultraviolet light therapy Finding site True Skin structure Inferred relationship Some 1
Adverse effect from PUVA photochemotherapy Finding site False Skin structure Inferred relationship Some 1
PUVA therapy-associated skin malignancy Finding site False Skin structure Inferred relationship Some 2
PUVA therapy-associated squamous cell carcinoma Finding site False Skin structure Inferred relationship Some 2
Bronze baby Finding site False Skin structure Inferred relationship Some 1
PUVA acne Finding site False Skin structure Inferred relationship Some 1
PUVA-induced pruritus Finding site True Skin structure Inferred relationship Some 1
Dermal-fat-fascia graft Procedure site - Direct (attribute) False Skin structure Inferred relationship Some 2
Allergic contact dermatitis caused by iodophore (disorder) Finding site True Skin structure Inferred relationship Some 1
Allergic contact dermatitis caused by povidone iodine (disorder) Finding site True Skin structure Inferred relationship Some 1
Progeroid syndrome, Petty type is a rare premature aging syndrome characterized by pre-and postnatal growth retardation, a congenital premature-aged appearance with distinctive craniofacial dysmorphism (wide calvaria with large open anterior fontanel and wide metopic suture, broad forehead, small face, micrognathia), markedly diminished subcutaneous fat, cutis laxa and wrinkled skin, without delay in psychomotor development. Scant, brittle hair, hypoplastic nails and delayed, abnormal dentition, as well as hypoplastic distal phalanges, umbilical hernia and eye abnormalities (myopia/hyperopia, strabismus), are also commonly associated. Finding site True Skin structure Inferred relationship Some 1
Allergic contact dermatitis caused by iodine (disorder) Finding site True Skin structure Inferred relationship Some 1
Epidermal burn of multiple sites Finding site True Skin structure Inferred relationship Some 1
Cutaneous rhinosporidiosis (disorder) Finding site True Skin structure Inferred relationship Some 1
Diffuse cutaneous leishmaniasis Finding site True Skin structure Inferred relationship Some 1
Recurrent cutaneous leishmaniasis Finding site True Skin structure Inferred relationship Some 1
Disseminated anergic leishmaniasis Finding site True Skin structure Inferred relationship Some 1
Classical zoonotic cutaneous leishmaniasis Finding site True Skin structure Inferred relationship Some 1
Indian anthroponotic cutaneous leishmaniasis Finding site True Skin structure Inferred relationship Some 1
Cutaneous toxoplasmosis Finding site True Skin structure Inferred relationship Some 1
Polypoid cutaneous rhinosporidiosis Finding site True Skin structure Inferred relationship Some 1
Lupoid leishmaniasis Finding site True Skin structure Inferred relationship Some 1
Middle Eastern zoonotic cutaneous leishmaniasis Finding site True Skin structure Inferred relationship Some 1
Wet form of cutaneous leishmaniasis Finding site True Skin structure Inferred relationship Some 1
Bush yaws Finding site True Skin structure Inferred relationship Some 1
Zoonotic form of cutaneous leishmaniasis Finding site True Skin structure Inferred relationship Some 1
American cutaneous/mucocutaneous Leishmaniasis (disorder) Finding site True Skin structure Inferred relationship Some 1
Post-kala-azar dermal leishmaniasis Finding site True Skin structure Inferred relationship Some 1
Indian zoonotic cutaneous leishmaniasis Finding site True Skin structure Inferred relationship Some 1
Late cutaneous leishmaniasis Finding site True Skin structure Inferred relationship Some 1
Sahelian zoonotic cutaneous leishmaniasis Finding site True Skin structure Inferred relationship Some 1
Infection by Leishmania aethiopica Finding site True Skin structure Inferred relationship Some 1
Leishmania brasiliensis complex cutaneous leishmaniasis (disorder) Finding site True Skin structure Inferred relationship Some 1
Diffuse cutaneous leishmaniasis caused by Leishmania aethiopica Finding site True Skin structure Inferred relationship Some 1
Dry form of cutaneous leishmaniasis Finding site True Skin structure Inferred relationship Some 1
Laser destruction of verruca Procedure site - Direct (attribute) True Skin structure Inferred relationship Some 1
Cutaneous leishmaniasis Finding site True Skin structure Inferred relationship Some 1
Diffuse cutaneous New World leishmaniasis (disorder) Finding site True Skin structure Inferred relationship Some 1
Infection by Leishmania tropica minor Finding site True Skin structure Inferred relationship Some 1
Leishmania recidiva (disorder) Finding site True Skin structure Inferred relationship Some 1
Trichomoniasis affecting skin (disorder) Finding site True Skin structure Inferred relationship Some 1
American trypanosomiasis affecting skin (disorder) Finding site True Skin structure Inferred relationship Some 1
Asian desert cutaneous leishmaniasis Finding site True Skin structure Inferred relationship Some 1
Hypertrichosis cubiti is a rare hair anomaly characterized by symmetrical, congenital or early-onset, bilateral hypertrichosis localized on the extensor surfaces of the upper extremities (especially the elbows). Short stature, or other abnormalities, such as developmental delay, facial anomalies and intellectual disability, may or may not be associated. Finding site False Skin structure Inferred relationship Some 3
X-linked reticulate pigmentary disorder is an extremely rare skin disease described in only four families to date and characterized in males by diffuse reticulate brown hyperpigmented skin lesions developing in early childhood and a variety of systemic manifestations (recurrent pneumonia, corneal opacification, gastrointestinal inflammation, urethral stricture, failure to thrive, hypohidrosis, digital clubbing, and unruly hair and flared eyebrows), while in females, there is only cutaneous involvement with the development in early childhood of localized brown hyperpigmented skin lesions following the lines of Blaschko. This disease was first considered as a cutaneous amyloidosis, but amyloid deposits are an inconstant feature. Finding site True Skin structure Inferred relationship Some 1
Pemphigus vulgaris of gingival mucous membrane (disorder) Finding site False Skin structure Inferred relationship Some 2
A rare superficial pemphigus disease characterized by severe intractable pruritus with erythematous or urticarial plaques and sometimes vesicles organized in a herpetiform pattern. Mucosae are generally spared. Eosinophilia in peripheral blood and low titers of circulating autoantibodies are observed in many cases. Histology can show an aspect of either pemphigus (superficial or deep), or an intraepidermal infiltrate rich in eosinophils (eosinophilic spongiosis). Finding site True Skin structure Inferred relationship Some 1
Congenital panfollicular nevus is a rare, benign, skin tumor disorder characterized by the presence of congenital, large (few centimeters), elevated, well-circumscribed, pink-tan, multinodular, non-ulcerative, bosselated-surface skin lesions located on the neck, scalp or hand and which enlarge with time. Histologically, hamartomatous proliferation containing irregularly arranged, malformed hair follicles in various stages of development, surrounded by fibrous tissue and densely distributed within the dermis is observed. Finding site True Skin structure Inferred relationship Some 1
Dermatitis as late effect of radiation (disorder) Finding site True Skin structure Inferred relationship Some 1
Occupational phototoxic reaction to skin contact with exogenous photoactive agent (disorder) Finding site True Skin structure Inferred relationship Some 1
Phototoxic reaction of skin caused by fragrance (disorder) Finding site True Skin structure Inferred relationship Some 1
Acute photoallergic dermatitis (disorder) Finding site False Skin structure Inferred relationship Some 2
Phototoxic reaction of skin caused by cosmetic Finding site True Skin structure Inferred relationship Some 1
Hidrotic ectodermal dysplasia, Christianson-Fourie type is a rare ectodermal dysplasia syndrome characterized by tricho- and onychodysplasia in association with cardiac rhythm abnormalities. Patients present with sparse scalp hair and eyelashes, absent or sparse eyebrows, dystrophic thickened nails (on fingers distal end may be lifted from the nail bed) and supraventricular tachycardia or sinus bradycardia. Finding site False Skin structure Inferred relationship Some 1
Leukoencephalopathy-palmoplantar keratoderma syndrome is a rare, genetic epidermal disease characterized by early childhood-onset of punctate palmoplantar keratoderma in association with adult-onset leukoencephalopathy manifested by progressive tetrapyramidal syndrome and cognitive deterioration. Finding site False Skin structure Inferred relationship Some 3
Thumb deformity-alopecia-pigmentation anomaly syndrome is a rare, genetic, congenital limb malformation syndrome characterized by short stature, sparse scalp hair, hypoplastic, proximally placed thumbs, and skin hyperpigmentation with areas of raindrop depigmentation. Presence of a single, upper central incisor has also been reported. There have been no further descriptions in the literature since 1988. Finding site True Skin structure Inferred relationship Some 2
Hereditary progressive mucinous histiocytosis is a rare, benign, non-Langerhans cell histiocytosis characterized by childhood or adolescence onset of multiple, small, asymptomatic, slowly progressing, skin-colored to red-brown papules with predilection for the face, dorsal hands, forearms and legs, without associated mucosal or visceral involvement. Histologically, papules are well-circumscribed, unencapsulated, nodular aggregates of histiocytes with abundant mucin in the upper and mid dermis. Finding site True Skin structure Inferred relationship Some 1
Hereditary sclerosing poikiloderma Finding site True Skin structure Inferred relationship Some 1
Pseudoleprechaunism syndrome, Patterson type is a rare, genetic, adrenal disorder characterized by congenital bronzed hyperpigmentation, cutis laxa of the hands and feet, body disproportion (comprising large hands, feet, nose and ears), hirsutism and severe intellectual disability. Patients additionally present hyperadrenocorticism, cushingoid features, premature adrenarche and diabetes mellitus, as well as skeletal deformities (not present at birth and which progress with age). There have been no further descriptions in the literature since 1981. Finding site True Skin structure Inferred relationship Some 1
Pilodental dysplasia-refractive errors syndrome is a rare ectodermal dysplasia syndrome characterized by dysplastic abnormalities of the hair and teeth (including hypodontia, abnormally shaped teeth, scalp hypotrichosis and pili annulati), follicular hyperkeratosis on the trunk and limbs, and hyperopia. Intensified delineation, reticular hyperpigmentation of the nape and astigmatism have also been reported. There have been no further descriptions in the literature since 1985. Finding site False Skin structure Inferred relationship Some 1
Cytomegalovirus infection of skin Finding site True Skin structure Inferred relationship Some 1
Human herpes virus 7 infection of skin (disorder) Finding site True Skin structure Inferred relationship Some 1
Extrasystoles-short stature-hyperpigmentation-microcephaly syndrome is a rare, genetic, malformation syndrome with short stature characterised by microcephaly, borderline intellectual disability, hyperpigmentation of the skin, short stature, and ventricular extrasystoles. Cardiac syncope may also be associated. There have been no further descriptions in the literature since 1975. Finding site True Skin structure Inferred relationship Some 1
Intermediate lesion of pinta Finding site True Skin structure Inferred relationship Some 1
Relapsing fever of North Africa Finding site True Skin structure Inferred relationship Some 1
Hyperkeratosis of pinta Finding site False Skin structure Inferred relationship Some 2
Cutaneous disorder caused by bovine papular stomatitis virus Finding site True Skin structure Inferred relationship Some 1
Neonatal viral infection of skin (disorder) Finding site True Skin structure Inferred relationship Some 1
Pinta, primary lesion Finding site True Skin structure Inferred relationship Some 1
Relapsing fever of Southwest U.S. AND/OR Mexico 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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