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238980001: Systemic disease affecting skin (disorder)


Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2019. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3773322014 Systemic disease affecting skin (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3773621012 Systemic disease affecting skin en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
2611000188115 pathologies systémiques avec manifestations cutanées fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


33 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Systemic disease affecting skin (disorder) Is a Disorder of skin (disorder) true Inferred relationship Some
Systemic disease affecting skin (disorder) Finding site Skin structure true Inferred relationship Some 1
Systemic disease affecting skin (disorder) Is a Systemic disease true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group
Meningococcal rash Is a False Systemic disease affecting skin (disorder) Inferred relationship Some
Disorder of soft tissue due to diabetes mellitus (disorder) Is a False Systemic disease affecting skin (disorder) Inferred relationship Some
Familial Mediterranean fever Is a False Systemic disease affecting skin (disorder) Inferred relationship Some
Glucagonoma syndrome Is a False Systemic disease affecting skin (disorder) Inferred relationship Some
Acquired epidermolysis bullosa Is a False Systemic disease affecting skin (disorder) Inferred relationship Some
Pyoderma gangrenosum (disorder) Is a False Systemic disease affecting skin (disorder) Inferred relationship Some
Acute febrile neutrophilic dermatosis Is a False Systemic disease affecting skin (disorder) Inferred relationship Some
Nephrogenic systemic fibrosis (disorder) Is a False Systemic disease affecting skin (disorder) Inferred relationship Some
CREST syndrome Is a True Systemic disease affecting skin (disorder) Inferred relationship Some
Systemic amyloidosis affecting skin (disorder) Is a True Systemic disease affecting skin (disorder) Inferred relationship Some
CRST syndrome Is a True Systemic disease affecting skin (disorder) Inferred relationship Some
Immunoglobulin A vasculitis Is a False Systemic disease affecting skin (disorder) Inferred relationship Some
A rare autoinflammatory syndrome with characteristics of the presence of features of relapsing polychondritis and Behcet disease in the same individual. This includes cartilage inflammation of the ears, nose, throat and rib cage as well as recurrent oral and genital ulcers respectively. Patients may also present ocular involvement (in particular anterior uveitis or scleritis), arthritis, fever, colitis, thrombophlebitis, and central nervous system vasculitis or in rare cases arterial aneurysms. Symptoms of polychondritis occur secondary to those of Behcet disease in the vast majority of cases. Is a False Systemic disease affecting skin (disorder) Inferred relationship Some
Cutaneous polyarteritis nodosa Is a True Systemic disease affecting skin (disorder) Inferred relationship Some
Severe systemic illness-induced cutaneous atrophy Is a True Systemic disease affecting skin (disorder) Inferred relationship Some
Rheumatoid arthritis with nailfold and finger-pulp infarcts (disorder) Is a False Systemic disease affecting skin (disorder) Inferred relationship Some
Necrotizing vasculitis due to mixed cryoglobulinemia (disorder) Is a True Systemic disease affecting skin (disorder) Inferred relationship Some
Lupus erythematosus-associated urticarial vasculitis (disorder) Is a False Systemic disease affecting skin (disorder) Inferred relationship Some
Drug-induced lymphocytic vasculitis (disorder) Is a False Systemic disease affecting skin (disorder) Inferred relationship Some
Infantile systemic hyalinosis (ISH) is a very rare disorder belonging to the heterogeneous group of genetic fibromatoses and is characterized by progressive joint contractures, skin abnormalities, severe chronic pain and widespread deposition of hyaline material in many tissues such as the skin, skeletal muscle, cardiac muscle, gastrointestinal tract, lymph nodes, spleen, thyroid, and adrenal glands. Is a False Systemic disease affecting skin (disorder) Inferred relationship Some
Behcet disease of skin (disorder) Is a True Systemic disease affecting skin (disorder) Inferred relationship Some
Mast cell leukemia affecting skin (disorder) Is a True Systemic disease affecting skin (disorder) Inferred relationship Some
Cutaneous complication of rheumatoid disease (disorder) Is a True Systemic disease affecting skin (disorder) Inferred relationship Some
Systemic onset juvenile chronic arthritis Is a False Systemic disease affecting skin (disorder) Inferred relationship Some
Adult onset Still's disease Is a True Systemic disease affecting skin (disorder) Inferred relationship Some
Crohn's disease of vulva (disorder) Is a True Systemic disease affecting skin (disorder) Inferred relationship Some
Crohn's disease of penis (disorder) Is a True Systemic disease affecting skin (disorder) Inferred relationship Some
Crohn's disease of scrotum (disorder) Is a True Systemic disease affecting skin (disorder) Inferred relationship Some
A rare genetic disease characterised by infantile or childhood onset of abnormal growth of hyalinised fibrous tissue, giving rise to multiple cutaneous nodules and/or pearly papules predominantly affecting the scalp, ears, neck, face, hands, and feet. Involvement of other organs results in gingival hyperplasia, osteolytic bone lesions, and joint contractures. Some patients exhibit visceral involvement with intractable diarrhoea, increased susceptibility to infections, and severe failure to thrive. Is a True Systemic disease affecting skin (disorder) Inferred relationship Some
Crohn's disease of parastomal skin Is a True Systemic disease affecting skin (disorder) Inferred relationship Some
A rare genetic systemic or rheumatologic disease characterized by infantile onset of skin anomalies (such as delayed wound healing with atrophic scars and mild alopecia with dry and brittle hair), retinal rod degeneration with night blindness, degenerative myopathy with muscle weakness, myalgia, and cramps, osteoarthritis, joint laxity, prolapse of internal organs, floating kidney syndrome, malabsorption syndrome, and hypothyroidism. The phenotype has been reported to be more severe in women than in men. Is a True Systemic disease affecting skin (disorder) Inferred relationship Some
A rare genetic autoinflammatory syndrome with skin involvement characterised by cold-induced urticarial rash without angioedema starting in infancy and systemic inflammation due to autosomal dominant mutations in the coagulation factor 12 (F-12) gene. In addition to cold-induced, non-pruritic urticarial rash, patients present with headache, mild to severe arthralgia, fatigue, subfebrile evening temperature, chills, and malaise. Systemic symptoms worsen during the cold season and over the years. Is a True Systemic disease affecting skin (disorder) Inferred relationship Some
Bullous systemic lupus erythematosus Is a True Systemic disease affecting skin (disorder) Inferred relationship Some
Rash of systemic lupus erythematosus Is a True Systemic disease affecting skin (disorder) Inferred relationship Some
Lupus panniculitis Is a True Systemic disease affecting skin (disorder) Inferred relationship Some
Lupus erythematosus-associated necrotizing vasculitis (disorder) Is a True Systemic disease affecting skin (disorder) Inferred relationship Some

This concept is not in any reference sets

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