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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
Infestation by Demodex phylloides Finding site False Skin structure Inferred relationship Some 2
Congenital diffuse lipomatosis Finding site True Skin structure Inferred relationship Some 1
Leprechaunism syndrome Finding site True Skin structure Inferred relationship Some 2
Neuropathic ulcer of toe due to type 2 diabetes mellitus (disorder) Finding site False Skin structure Inferred relationship Some 4
Neuropathic ulcer of foot due to type 2 diabetes mellitus (disorder) Finding site False Skin structure Inferred relationship Some 4
Pigmented purpuric lichenoid dermatitis of Gougerot and Blum Finding site True Skin structure Inferred relationship Some 6
Cutaneous diphtheria Finding site True Skin structure Inferred relationship Some 1
Benign lymphocytic infiltration of Jessner Finding site True Skin structure Inferred relationship Some 2
Giant cell pneumonia Finding site True Skin structure Inferred relationship Some 1
Pneumonia due to measles (disorder) Finding site True Skin structure Inferred relationship Some 1
Neuropathic ulcer of foot due to diabetes mellitus (disorder) Finding site False Skin structure Inferred relationship Some 4
Removal of leeches (procedure) Procedure site - Indirect (attribute) True Skin structure Inferred relationship Some 1
Eruptive collagenoma Finding site False Skin structure Inferred relationship Some 2
Familial cutaneous collagenoma Finding site False Skin structure Inferred relationship Some 2
Psoriatic arthritis with distal interphalangeal joint involvement Finding site False Skin structure Inferred relationship Some 5
Francois syndrome Finding site True Skin structure Inferred relationship Some 1
Dry skin dermatitis Finding site False Skin structure Inferred relationship Some 2
Gonococcal arthritis dermatitis syndrome Finding site True Skin structure Inferred relationship Some 2
Psoriasis of nail Finding site True Skin structure Inferred relationship Some 3
Psoriatic nail dystrophy (disorder) Finding site True Skin structure Inferred relationship Some 2
Psoriatic nail pitting Finding site True Skin structure Inferred relationship Some 2
Neonatal adnexal polyp Finding site True Skin structure Inferred relationship Some 2
Platinum sensitivity Finding site True Skin structure Inferred relationship Some 2
Skin disease attributable to corticosteroid therapy (disorder) Finding site True Skin structure Inferred relationship Some 1
Vulval lichen sclerosus, childhood form (disorder) Finding site False Skin structure Inferred relationship Some 2
Lepromatous anterior uveitis (disorder) Finding site True Skin structure Inferred relationship Some 2
Seborrhoeic keratosis Finding site True Skin structure Inferred relationship Some 1
Lichen sclerosus of female genitalia Finding site False Skin structure Inferred relationship Some 2
Anetoderma secondary to syphilis (disorder) Finding site True Skin structure Inferred relationship Some 1
Tar keratosis (disorder) Finding site True Skin structure Inferred relationship Some 1
Juvenile xanthogranuloma of skin (disorder) Finding site True Skin structure Inferred relationship Some 1
Werner syndrome Finding site True Skin structure Inferred relationship Some 1
Lipogranulomatosis subcutanea of Rothmann and Makai Finding site True Skin structure Inferred relationship Some 6
Izumi fever Finding site True Skin structure Inferred relationship Some 2
Chronic migratory panniculitis Finding site False Skin structure Inferred relationship Some 6
Perinatal cutaneous ecchymoses Finding site True Skin structure Inferred relationship Some 1
Perinatal cutaneous petechiae (disorder) Finding site True Skin structure Inferred relationship Some 1
Pigmented actinic keratosis (disorder) Finding site True Skin structure Inferred relationship Some 1
Hyperkeratotic actinic keratosis Finding site True Skin structure Inferred relationship Some 1
Inflamed seborrheic keratosis (disorder) Finding site True Skin structure Inferred relationship Some 2
Superficial ulcer of skin of pacemaker pulse generator site Finding site True Skin structure Inferred relationship Some 1
Painful pigmented pressure papules Finding site True Skin structure Inferred relationship Some 1
A rare malformation syndrome characterized by generalized multiple steatocystomas and natal teeth. Finding site True Skin structure Inferred relationship Some 2
A rare inflammatory bowel disease characterized by early cutaneous photosensitivity manifesting by sun-induced facial erythematous and vesicular lesions and severe recurrent colitis which lead to untreatable diarrhea. There have been no further descriptions in the literature since 1991. Finding site True Skin structure Inferred relationship Some 1
A rare arthrogryposis syndrome characterized by the association of multiple congenital joint contractures (of the large joints, fingers and toes) and hyperkeratosis (i.e. thick, scaling and fissured skin), with death occurring in early infancy. There have been no further reports in the literature since 1993. Finding site True Skin structure Inferred relationship Some 3
Change of diaper (procedure) Procedure site - Indirect (attribute) True Skin structure Inferred relationship Some 1
schwannomatose Finding site False Skin structure Inferred relationship Some 3
A rare secondary neonatal autoimmune disease characterized by generalized weakness, severe hypotonia, absent or reduced deep tendon reflexes, and highly elevated serum creatine kinase levels presenting in the neonatal period. Perifascicular atrophy in the presence of a diffuse perivascular inflammatory cell exudate is observed on muscle biopsy. Finding site True Skin structure Inferred relationship Some 2
Spitzoid neoplasm of uncertain malignant potential (disorder) Finding site True Skin structure Inferred relationship Some 1
Acquired cutaneous lymphangiectasia Finding site True Skin structure Inferred relationship Some 2
Congenital cutaneous lymphangiectasia Finding site False Skin structure Inferred relationship Some 2
Amoeboma of skin Finding site True Skin structure Inferred relationship Some 1
Primary cutaneous CD4 positive small and medium T-cell lymphoproliferative disorder (disorder) Finding site True Skin structure Inferred relationship Some 1
Chronic excoriation of skin (disorder) Finding site True Skin structure Inferred relationship Some 1
Cutaneous insect bite reaction Finding site True Skin structure Inferred relationship Some 1
Irritant contact blepharoconjunctivitis Finding site False Skin structure Inferred relationship Some 3
Late manifestations of infection of skin caused by Borrelia (disorder) Finding site True Skin structure Inferred relationship Some 1
Late syphilis of skin Finding site True Skin structure Inferred relationship Some 1
Malignant pilonidal cyst Finding site False Skin structure Inferred relationship Some 1
Malignant pilonidal cyst Finding site False Skin structure Inferred relationship Some 2
Necrobiotic granulomatous skin disorder Finding site True Skin structure Inferred relationship Some 1
Squamous cell carcinoma in situ of skin caused by sunlight (disorder) Finding site True Skin structure Inferred relationship Some 1
Focal facial dermal dysplasias (FFDD) are rare ectodermal dysplasias, characterized by congenital bitemporal (resembling forceps marks) or preauricular scar-like lesions associated with additional facial and or systematic manifestations. 4 types of FFDD are described. FFDD types II and III present with a variable facial dysmorphism including distichiasis (upper lashes) or lacking eyelashes, and upward slanting and thinned lateral eyebrows with a flattened nasal bridge and full upper lip. FFDD types I and IV are infrequently associated with extra-cutaneous anomalies. Finding site True Skin structure Inferred relationship Some 2
Focal facial dermal dysplasia type I (FFDD1), also known as Brauer syndrome, is a focal facial dysplasia with characteristics of congenital bitemporal cutis aplasia. The bitemporal rarely unilateral hypoplastic scar-like lesions in FFDD, resembling forceps marks, are usually the only manifestations of FFDD1. Most patients usually have normal intelligence. Transmitted in an autosomal dominant manner with full penetrance. Finding site True Skin structure Inferred relationship Some 2
Focal facial dermal dysplasia type II (FFDD2) is a focal facial dermal dysplasia with characteristics of congenital bitemporal scar-like depressions with additional facial dysmorphic features. Cardiac and genital or urinary abnormalities have been rarely noted. Developmental delay, severe intellectual disability, behavioural problems, and learning difficulties may be observed. Transmitted in an autosomal dominant manner with variable expressivity and incomplete penetrance. Finding site True Skin structure Inferred relationship Some 2
Focal facial dermal dysplasia type III (FFDD3) is a rare focal facial dermal dysplasia with primary characteristics of congenital bitemporal scar-like depressions and a typical but variable facial dysmorphism. Caused by homozygous mutations in the TWIST2 gene, which encodes a bHLH transcription factor involved in dermal facial development in mammals. However, the majority of unrelated FFDD3 patients evaluated have had normal TWIST2 sequences, indicating the molecular genetic heterogeneity of the disorder. Many cases are sporadic. Inheritance is autosomal recessive for patients with TWIST2 mutations. Finding site True Skin structure Inferred relationship Some 2
Focal facial dermal dysplasia type IV (FFDD4) is a rare focal facial dysplasia with characteristics of congenital isolated preauricular and/or cheek blister scar-like lesions. Affected FFDD4 patients typically do not present with extra-cutaneous manifestations, although in a small number of cases, a hair collar sign (circumscription of the cutaneous lesion with terminal hairs), polyps on the buccal mucosa with a similar distribution pattern, and developmental delay have been reported. An autosomal recessive trait. Finding site True Skin structure Inferred relationship Some 2
Pimple of skin Finding site True Skin structure Inferred relationship Some 1
Neuropathic ulcer of heel due to type 2 diabetes mellitus Finding site False Skin structure Inferred relationship Some 4
Neuropathic ulcer of midfoot due to type 2 diabetes mellitus Finding site False Skin structure Inferred relationship Some 4
Injection site dermatitis Finding site True Skin structure Inferred relationship Some 3
Rough skin (finding) Finding site True Skin structure Inferred relationship Some 1
Sinus of skin following surgical procedure Finding site True Skin structure Inferred relationship Some 1
Suppurative sinus of skin Finding site True Skin structure Inferred relationship Some 1
Suppurative sinus of skin Finding site True Skin structure Inferred relationship Some 2
Skin specimen obtained by excision, frozen section (specimen) Specimen source topography True Skin structure Inferred relationship Some 1
Exogenous dermatitis Finding site True Skin structure Inferred relationship Some 1
Ochronosis caused by hydroquinone (disorder) Finding site True Skin structure Inferred relationship Some 1
Exogenous ochronosis (disorder) Finding site True Skin structure Inferred relationship Some 1
Ochronosis due to homogentisate 1,2-dioxygenase deficiency (disorder) Finding site True Skin structure Inferred relationship Some 1
Familial granulomatous inflammatory arthritis, dermatitis and uveitis (disorder) Finding site True Skin structure Inferred relationship Some 3
Poikiloderma of Civatte Finding site True Skin structure Inferred relationship Some 2
Normal color of skin over lesion (finding) Finding site True Skin structure Inferred relationship Some 1
On examination - skin over lesion hot Finding site False Skin structure Inferred relationship Some 1
Hot skin over lesion Finding site True Skin structure Inferred relationship Some 1
Cold skin over lesion Finding site True Skin structure Inferred relationship Some 1
On examination - skin over lesion cold Finding site False Skin structure Inferred relationship Some 1
Warm skin over lesion Finding site True Skin structure Inferred relationship Some 1
On examination - skin over lesion warm Finding site False Skin structure Inferred relationship Some 1
Normal temperature of skin over lesion Finding site True Skin structure Inferred relationship Some 1
Redness of skin over lesion Finding site True Skin structure Inferred relationship Some 1
On examination - skin red over lesion Finding site False Skin structure Inferred relationship Some 1
Atrophic lichen planus Finding site True Skin structure Inferred relationship Some 4
Pigmented purpuric lichenoid dermatitis of Gougerot and Blum Finding site True Skin structure Inferred relationship Some 7
Oral lichen planus Finding site True Skin structure Inferred relationship Some 4
Lichen planus-lupus erythematosus overlap Finding site True Skin structure Inferred relationship Some 5
Lichen planus of scalp Finding site True Skin structure Inferred relationship Some 4
Lichen planus of palms and soles Finding site True Skin structure Inferred relationship Some 4
Ulcerative lichen planus of palms and soles Finding site True Skin structure Inferred relationship Some 4
Nail pterygium in lichen planus (disorder) Finding site True Skin structure Inferred relationship Some 4
Mutilating lichen planus of fingers and toes Finding site True Skin structure Inferred relationship Some 4

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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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