FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.22-SNAPSHOT  |  FHIR Version n/a  User: [n/a]

128236002: Chronic disease of skin (disorder)

Status: current, 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
206487017 Chronic skin disease en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
206488010 Chronic dermatosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
206489019 Chronic disease of skin en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
732204016 Chronic disease of skin (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
109591000077119 maladie chronique de la peau fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

163 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Chronic disease of skin Is a Chronic disease true Inferred relationship Some
Chronic disease of skin Is a Disorder of skin (disorder) true Inferred relationship Some
Chronic disease of skin Finding site Skin structure true Inferred relationship Some 2
Chronic disease of skin Course Chronic false Inferred relationship Some
Chronic disease of skin Clinical course Chronic true Inferred relationship Some 1
Inbound Relationships Type Active Source Characteristic Refinability Group
Adult onset Still's disease Is a True Chronic disease of skin Inferred relationship Some
Sclerodermoid chronic graft-versus-host disease (disorder) Is a True Chronic disease of skin Inferred relationship Some
Rubeosis faciei due to diabetes mellitus (disorder) Is a True Chronic disease of skin Inferred relationship Some
Progressive nodular histiocytosis is a rare, normolipemic, non-Langerhans cell histiocytosis characterized by progressive growth of multiple to disseminated, asymptomatic skin lesions that range in appearance from yellow plaques to coalescence-prone red-brown papules, nodules and pedunculated tumors up to 5 cm in size, located typically on the face, trunk and extremities (and rarely on conjunctiva and mucous membranes). Characteristic microscopic findings include a storiform spindle cell infiltrate in the deep dermis with xanthomatous macrophages and some Touton cells in the upper dermis. It is usually not associated with systemic disease. Is a True Chronic disease of skin Inferred relationship Some
Hemodialysis-associated secondary amyloidosis of skin (disorder) Is a True Chronic disease of skin Inferred relationship Some
A rare monogenic form of cutaneous lupus erythematosus characterised by infantile or childhood onset of cold-induced erythematous papules or plaques predominantly on the fingers, toes, nose, cheeks, and ears. Recurrent ulceration of the lesions may lead to necrotic tissue destruction and mutilation. Patients may experience ischaemia of the affected acral regions. Histological findings include cutaneous perivascular inflammatory infiltrates with deposits of immunoglobulins or complement. Is a True Chronic disease of skin Inferred relationship Some
Pigmented purpuric dermatosis (disorder) Is a True Chronic disease of skin Inferred relationship Some
Progressive macular hypomelanosis Is a True Chronic disease of skin Inferred relationship Some
Recurrent venous ulcer of lower limb Is a False Chronic disease of skin Inferred relationship Some
Chronic prurigo Is a True Chronic disease of skin Inferred relationship Some
Extragenital lichen sclerosus and morphea (disorder) Is a True Chronic disease of skin Inferred relationship Some
Chronic coalescent cutaneous lobomycosis Is a True Chronic disease of skin Inferred relationship Some
Lipoid dermatoarthritis Is a True Chronic disease of skin Inferred relationship Some
A rare systemic disease characterized by generalized joint hypermobility with recurrent joint dislocations, redundant and hyperextensible skin with poor wound healing and abnormal scarring, easy bruising, and osteopenia/osteoporosis. Additional manifestations include hypotonia, delayed motor development, foot deformities, prominent superficial veins in the chest region, vascular complications (like mitral valve prolapse and aortic root dilation), hernias, dental anomalies, scoliosis, and facial dysmorphisms (like high palate, micrognathia, narrow palate). Mode of inheritance is autosomal recessive. Is a False Chronic disease of skin Inferred relationship Some
A rare inherited cancer-predisposing syndrome characterized by skin lesions, kidney tumors, and pulmonary cysts that may be associated with pneumothorax. The kidney tumors range from benign oncocytomas to malignant renal cell carcinomas including chromophobe, clear cell or papillary subtypes. Fibrofolliculomas are characterized by a circumscribed proliferation of collagen and fibroblasts surrounding distorted hair follicles from which basaloid cells protrude into the surrounding fibromucinous stroma. Other characteristic skin anomalies are trichodiscomas and acrochordons. Dermatological manifestations usually develop in the third and fourth decades of life and persist indefinitely. The syndrome is transmitted in an autosomal dominant fashion. Is a True Chronic disease of skin Inferred relationship Some
Skin changes due to chronic exposure to non-ionizing radiation Is a True Chronic disease of skin Inferred relationship Some
Exacerbation of psoriasis (disorder) Is a True Chronic disease of skin Inferred relationship Some
A rare syndromic optic nerve hypoplasia with characteristics of coloboma, osteopetrosis (particularly of the anterior ribs and femoral heads), severe microphthalmia, macrocephaly, albinism, and profound congenital deafness. Patients may also have additional eye anomalies including microcornea with pannus, dense bilateral cataracts, and translucent irides. Craniofacial dysmorphism (including frontal bossing, shallow orbits, preauricular pits, posteriorly rotated ears, micrognathia and wide palatine ridges) is also reported. Is a True Chronic disease of skin Inferred relationship Some
Sun-induced wrinkles (disorder) Is a True Chronic disease of skin Inferred relationship Some
A rare hyper-IgE syndrome with characteristics of atopic dermatitis (eczema), chronic mucocutaneous candidiasis, and elevated IgE levels due to ZNF341 deficiency. High plasma levels of IgG and low natural killer (NK) cell numbers are observed. Other major clinical features involve recurrent skin infections with skin abscesses and connective tissue abnormalities. Some patients may have recurrent lung infections. Is a True Chronic disease of skin Inferred relationship Some
Multiple sclerosis-ichthyosis-factor VIII deficiency syndrome is characterized by the association of multiple sclerosis with lamellar ichthyosis and hematological anomalies (beta thalassemia minor and a quantitative deficit of factor VIII-von Willebrand complex). Other clinical manifestations may include eye involvement (optic atrophy, diplopia), neuromuscular involvement (ataxia, pyramidal syndrome, gait disturbance) and sensory disorder. There have been no further descriptions in the literature since 1992. Is a True Chronic disease of skin Inferred relationship Some

Start Page 2 of 2

This concept is not in any reference sets

Back to Start