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70819003: Erythema (morphologic abnormality)

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
117640019 Erythema en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
810916018 Erythema (morphologic abnormality) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
1080921000241114 érythème fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

3 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Erythema Is a Eruption true Inferred relationship Some
Inbound Relationships Type Active Source Characteristic Refinability Group
Erythema papulatum Associated morphology False Erythema Inferred relationship Some 1
Erythema dyschromicum perstans Associated morphology False Erythema Inferred relationship Some 1
Erythema annulare centrifugum (disorder) Associated morphology False Erythema Inferred relationship Some 1
Drug-induced Stevens-Johnson syndrome Associated morphology False Erythema Inferred relationship Some 1
Staphylococcal intertrigo Associated morphology False Erythema Inferred relationship Some 1
Erythroderma caused by vancomycin Associated morphology False Erythema Inferred relationship Some 2
Roseolar erythema (disorder) Associated morphology False Erythema Inferred relationship Some 1
Streptococcal intertrigo Associated morphology False Erythema Inferred relationship Some 1
Erythema multiforme Associated morphology True Erythema Inferred relationship Some 1
Other specified erythema multiforme Associated morphology False Erythema Inferred relationship Some 1
Erythema multiforme NOS Associated morphology False Erythema Inferred relationship Some 1
A type of superficial inflammatory dermatitis occurring where two skin surfaces are in apposition. Intertrigo occurs in the skin fold and results from friction, heat, moisture and may lead to skin infection. Associated morphology False Erythema Inferred relationship Some 1
Erythema vesiculosum Associated morphology False Erythema Inferred relationship Some 1
Candidal intertrigo Associated morphology False Erythema Inferred relationship Some 1
Diffuse inflammatory erythema (disorder) Associated morphology False Erythema Inferred relationship Some 1
Persistent erythema of skin Associated morphology True Erythema Inferred relationship Some 1
Erythema tuberculatum Associated morphology False Erythema Inferred relationship Some 1
Familial annular erythema Associated morphology False Erythema Inferred relationship Some 1
Primary erythromelalgia (disorder) Associated morphology False Erythema Inferred relationship Some 1
Erythema of mucous membrane of oral vestibule Associated morphology True Erythema Inferred relationship Some 1
Oral erythematous candidiasis Associated morphology True Erythema Inferred relationship Some 1
Erythema urticatum Associated morphology False Erythema Inferred relationship Some 1
Erythematous mucosa Associated morphology False Erythema Inferred relationship Some 1
Erythema multiforme of pregnancy Associated morphology True Erythema Inferred relationship Some 1
Erythema multiforme, epidermal type (disorder) Associated morphology True Erythema Inferred relationship Some 1
Annular erythema caused by drug (disorder) Associated morphology False Erythema Inferred relationship Some 1
Erythema multiforme due to malignancy (disorder) Associated morphology True Erythema Inferred relationship Some 1
Acral erythema due to cytotoxic therapy (disorder) Associated morphology False Erythema Inferred relationship Some 1
Annular erythema Associated morphology False Erythema Inferred relationship Some 1
Erythema fugax Associated morphology False Erythema Inferred relationship Some 1
Erythema marginatum in acute rheumatic fever Associated morphology False Erythema Inferred relationship Some 1
Erythema chronica migrans Associated morphology False Erythema Inferred relationship Some 1
Primate erythroparvovirus 1 infection (disorder) Associated morphology False Erythema Inferred relationship Some 1
Erythema at injection site Associated morphology True Erythema Inferred relationship Some 1
État érythémateux Associated morphology False Erythema Inferred relationship Some 1
A limited form of Stevens-Johnson syndrome/toxic epidermal necrolysis spectrum characterised by destruction and detachment of the skin epithelium, involving less than 10% of the body surface area, and mucous membranes. Onset usually occurs 4-28 days after administration of the causal medication and is most frequently associated with anticonvulsants, antibacterial sulfonamides, allopurinol, nevirapine, and oxicams (non-steroidal anti-inflammatory drugs), but many other medications have also been implicated. The disease is not induced by medication in 15% of cases. Histology is characterised by an epidermal necrolysis. Multiple disabling long-term sequelae (especially cutaneous, ocular and psychological) are frequent. Associated morphology False Erythema Inferred relationship Some 1
[X]Erythema in other diseases classified elsewhere Associated morphology False Erythema Inferred relationship Some 1
Herpes iris Associated morphology True Erythema Inferred relationship Some 1
Candidiasis of finger web Associated morphology False Erythema Inferred relationship Some 1
Secondary erythromelalgia (disorder) Associated morphology False Erythema Inferred relationship Some 1
Exanthematous disorder Associated morphology True Erythema Inferred relationship Some 1
Periorbital erythema Associated morphology True Erythema Inferred relationship Some 1
Granulosis rubra nasi Associated morphology False Erythema Inferred relationship Some 1
Palmar erythema Associated morphology True Erythema Inferred relationship Some 1
érythème médicamenteux Associated morphology False Erythema Inferred relationship Some 1
Necrolytic migratory erythema Associated morphology False Erythema Inferred relationship Some 1
Erythema elevatum diutinum Associated morphology True Erythema Inferred relationship Some 1
érythème médicamenteux Associated morphology False Erythema Inferred relationship Some 1
érythème noueux lépreux Associated morphology False Erythema Inferred relationship Some 1
Lipogranulomatosis subcutanea of Rothmann and Makai Associated morphology False Erythema Inferred relationship Some 2
Acute erythema Associated morphology True Erythema Inferred relationship Some 1
Erythema Associated morphology True Erythema Inferred relationship Some 1
Idiopathic erythema Associated morphology True Erythema Inferred relationship Some 1
Chronic erythema Associated morphology True Erythema Inferred relationship Some 1
Erythema of skin Associated morphology False Erythema Inferred relationship Some 1
Erythema of skin Associated morphology True Erythema Inferred relationship Some 1
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). Associated morphology False Erythema Inferred relationship Some 1
Coccidioidomycosis with erythema multiforme Associated morphology True Erythema Inferred relationship Some 3
Erythema multiforme co-occurrent with ulcer of oral mucous membrane Associated morphology False Erythema Inferred relationship Some 3
Less serious form of hypersensitivity reaction which occurs in response to medicines, infections, or illness. Associated morphology False Erythema Inferred relationship Some 2
Severe mucocutaneous reactions; skin detachment of 10 to 30 percent of body surface area most commonly triggered by medications, characterised by extensive necrosis and detachment of the epidermis. Associated morphology False Erythema Inferred relationship Some 3
Erythema multiforme, mixed dermal-epidermal type Associated morphology True Erythema Inferred relationship Some 2
Drug-induced Stevens-Johnson syndrome Associated morphology True Erythema Inferred relationship Some 4
Generalized pustular psoriasis, exanthematous type Associated morphology True Erythema Inferred relationship Some 2
Chronic migratory panniculitis Associated morphology False Erythema Inferred relationship Some 4
Gingival disease due to erythema multiforme Associated morphology False Erythema Inferred relationship Some 3
Linear gingival erythema Associated morphology True Erythema Inferred relationship Some 1
Linear gingival erythema caused by fungus (disorder) Associated morphology False Erythema Inferred relationship Some 3
Acute erythematous eruption of skin Associated morphology True Erythema Inferred relationship Some 2
Neonatal erythroderma Associated morphology True Erythema Inferred relationship Some 2
A limited form of Stevens-Johnson syndrome/toxic epidermal necrolysis spectrum characterised by destruction and detachment of the skin epithelium, involving less than 10% of the body surface area, and mucous membranes. Onset usually occurs 4-28 days after administration of the causal medication and is most frequently associated with anticonvulsants, antibacterial sulfonamides, allopurinol, nevirapine, and oxicams (non-steroidal anti-inflammatory drugs), but many other medications have also been implicated. The disease is not induced by medication in 15% of cases. Histology is characterised by an epidermal necrolysis. Multiple disabling long-term sequelae (especially cutaneous, ocular and psychological) are frequent. Associated morphology True Erythema Inferred relationship Some 4
Stevens-Johnson and toxic epidermal necrolysis overlap syndrome caused by drug (disorder) Associated morphology True Erythema Inferred relationship Some 11
Severe mucocutaneous reactions; skin detachment of 10 to 30 percent of body surface area most commonly triggered by medications, characterised by extensive necrosis and detachment of the epidermis. Associated morphology True Erythema Inferred relationship Some 1
Rubeola scarlatinosa Associated morphology True Erythema Inferred relationship Some 1
Dukes-Filatow disease Associated morphology False Erythema Inferred relationship Some 1
Streptococcal toxin-mediated perineal erythema Associated morphology True Erythema Inferred relationship Some 1
Parapsoriasis lichenoides Associated morphology True Erythema Inferred relationship Some 3
Small plaque parapsoriasis Associated morphology True Erythema Inferred relationship Some 4
Parapsoriasis en plaques Associated morphology True Erythema Inferred relationship Some 4
Large plaque parapsoriasis Associated morphology True Erythema Inferred relationship Some 4
Parapsoriasis Associated morphology True Erythema Inferred relationship Some 3
Parapsoriasis atrophicans Associated morphology True Erythema Inferred relationship Some 3
Parapsoriasis herpetiformis Associated morphology True Erythema Inferred relationship Some 3
Parapsoriasis papulata Associated morphology True Erythema Inferred relationship Some 3
Parapsoriasis varioliformis Associated morphology True Erythema Inferred relationship Some 3
Erythema of mucous membrane of mouth due to and following traumatic injury (disorder) Associated morphology True Erythema Inferred relationship Some 3
Mucous membrane erythema Associated morphology True Erythema Inferred relationship Some 1
Erythema multiforme due to viral disease (disorder) Associated morphology True Erythema Inferred relationship Some 1
Necrolytic acral erythema (disorder) Associated morphology True Erythema Inferred relationship Some 3
Erythema palmare hereditarium is a rare, benign, congenital genetic skin disorder characterised by permanent and asymptomatic erythema of the palmar and, less frequently, the solar surfaces. In most cases, it presents with sharply demarcated redness of the thenar and hypothenar eminences, as well as the palmar aspect of the phalanges, with scattered telangiectasia spots that do not cause any discomfort (pain, itching or burning) to the patient. Associated morphology True Erythema Inferred relationship Some 1
Roseola infantum caused by human herpesvirus 6 Associated morphology False Erythema Inferred relationship Some 3
Hemorrhagic rubella Associated morphology True Erythema Inferred relationship Some 1
Rubella in mother complicating pregnancy, childbirth AND/OR puerperium Associated morphology True Erythema Inferred relationship Some 1
rubéole maternelle durant la grossesse : bébé pas encore accouché Associated morphology False Erythema Inferred relationship Some 1
Roseola infantum caused by human herpesvirus 7 Associated morphology False Erythema Inferred relationship Some 3
Pneumonia due to measles (disorder) Associated morphology True Erythema Inferred relationship Some 1
Subacute sclerosing panencephalitis Associated morphology False Erythema Inferred relationship Some 2
Varicella Associated morphology False Erythema Inferred relationship Some 2
Rubella pneumonia (disorder) Associated morphology False Erythema Inferred relationship Some 2
maladie virale caractérisée par un exanthème Associated morphology False Erythema Inferred relationship Some 1
Exanthema subitum Associated morphology False Erythema Inferred relationship Some 2

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