FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.8.2  |  FHIR Version n/a  User: [n/a]

95329006: Autoimmune skin disease (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
157909010 Autoimmune skin disease en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
839459017 Autoimmune skin disease (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
1235900011 Autoimmune diseases affecting skin en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
2002881000005114 Autoimmun hudsygdom da Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Danish module (core metadata concept)


115 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Autoimmune skin disease Is a Autoimmune disease true Inferred relationship Some
Autoimmune skin disease Is a Disorder of skin (disorder) true Inferred relationship Some
Autoimmune skin disease Finding site Skin structure false Inferred relationship Some
Autoimmune skin disease Finding site Structure of immune system (body structure) false Inferred relationship Some
Autoimmune skin disease Pathological process (attribute) Autoimmune process false Inferred relationship Some
Autoimmune skin disease Has definitional manifestation Immune system finding false Inferred relationship Some
Autoimmune skin disease Finding site Skin structure true Inferred relationship Some 1
Autoimmune skin disease Pathological process (attribute) Autoimmune process true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group
Dermatitis herpetiformis Is a False Autoimmune skin disease Inferred relationship Some
Thyroid-associated dermopathy Is a False Autoimmune skin disease Inferred relationship Some
Sclerodermiform reaction Is a True Autoimmune skin disease Inferred relationship Some
Eosinophilic cellulitis Is a False Autoimmune skin disease Inferred relationship Some
Eosinophilic spongiosis Is a True Autoimmune skin disease Inferred relationship Some
Postinfective immunoglobulin A vasculitis (disorder) Is a False Autoimmune skin disease Inferred relationship Some
Benign lymphocytic infiltration of Jessner Is a True Autoimmune skin disease Inferred relationship Some
Idiopatisk trombocytopenisk purpura Is a False Autoimmune skin disease Inferred relationship Some
Mixed collagen vascular disease Is a False Autoimmune skin disease Inferred relationship Some
Dermatomyositis Is a False Autoimmune skin disease Inferred relationship Some
Pemphigus Is a False Autoimmune skin disease Inferred relationship Some
Cutaneous lupus erythematosus Is a True Autoimmune skin disease Inferred relationship Some
Kutan anafylaksi Is a False Autoimmune skin disease Inferred relationship Some
Pemphigoid Is a False Autoimmune skin disease Inferred relationship Some
Linear IgA dermatosis Is a True Autoimmune skin disease Inferred relationship Some
Rash of systemic lupus erythematosus Is a False Autoimmune skin disease Inferred relationship Some
[X]Bullous disorders Is a False Autoimmune skin disease Inferred relationship Some
Dermatitis herpetiformis Is a False Autoimmune skin disease Inferred relationship Some
A rare genetic disease that manifests in childhood or early adolescence with a combination of chronic mucocutaneous candidiasis, hypoparathyroidism and autoimmune adrenal failure. The first manifestation of the disease (usually candidiasis) occurs in childhood with other manifestations appearing progressively. The most common autoimmune endocrine involvement is hypoparathyroidism (79-96% of cases). Adrenal failure most often manifests with concurrent mineralocorticoid and glucocorticoid deficiency (78% of cases). The disease is caused by mutations of the AIRE gene (21q22.3) coding for the AIRE transcription factor, which is involved in immune tolerance mechanisms and contributes to the negative selection of autoreactive T lymphocytes in the thymus, lymph nodes and spleen. Transmission is autosomal recessive. Is a False Autoimmune skin disease Inferred relationship Some
Immunoglobulin A vasculitis Is a False Autoimmune skin disease Inferred relationship Some
Dermatomyositis (disorder) Is a False Autoimmune skin disease Inferred relationship Some
Mixed collagen vascular disease (disorder) Is a True Autoimmune skin disease Inferred relationship Some
Acquired epidermolysis bullosa Is a True Autoimmune skin disease Inferred relationship Some
Toxic diffuse goiter with acropachy Is a False Autoimmune skin disease Inferred relationship Some
Toxic diffuse goiter with pretibial myxedema Is a False Autoimmune skin disease Inferred relationship Some
Herpes gestationis Is a False Autoimmune skin disease Inferred relationship Some
Conjunctivitis associated with autoimmune skin disorder (disorder) Is a False Autoimmune skin disease Inferred relationship Some
Postinfective immunoglobulin A vasculitis (disorder) Is a False Autoimmune skin disease Inferred relationship Some
Acute haemorrhagic oedema of childhood Is a False Autoimmune skin disease Inferred relationship Some
Conjunctivitis associated with autoimmune skin disorder (disorder) Associated with True Autoimmune skin disease Inferred relationship Some 2
Conjunctivitis associated with epidermolysis bullosa (disorder) Associated with True Autoimmune skin disease Inferred relationship Some 3
Conjunctivitis due to lichen planus (disorder) Associated with True Autoimmune skin disease Inferred relationship Some 3
Pemphigus/pemphigoid screening (procedure) Has focus False Autoimmune skin disease Inferred relationship Some
sklerodermi Is a False Autoimmune skin disease Inferred relationship Some
CREST syndrome Is a False Autoimmune skin disease Inferred relationship Some
CRST syndrome Is a False Autoimmune skin disease Inferred relationship Some
autoimmun progesteron dermatit/urticaria Is a False Autoimmune skin disease Inferred relationship Some
Pyogenic arthritis-pyoderma gangrenosum-acne syndrome is a rare pleiotropic autoinflammatory disorder of childhood, primarily affecting the joints and skin. Is a False Autoimmune skin disease Inferred relationship Some
Juvenil dermatitis herpetiformis Is a False Autoimmune skin disease Inferred relationship Some
Senil dermatitis herpetiformis Is a False Autoimmune skin disease Inferred relationship Some
A very rare secondary neonatal autoimmune disease characterised by generalised 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. Is a True Autoimmune skin disease Inferred relationship Some
Satoyoshi syndrome is a rare, multisystemic autoimmune disease mainly characterized by intermittent painful muscle spasms, alopecia (totalis or universalis in most cases) and long-lasting diarrhea that could lead to malnutrition, growth retardation, and amenorrhea. Secondary bone deformities and various endocrine anomalies may also be associated. Antinuclear antibodies are reported in many cases. Is a True Autoimmune skin disease Inferred relationship Some
Pemphigus foliaceus Is a True Autoimmune skin disease Inferred relationship Some
Autoimmune progesterone dermatitis Is a True Autoimmune skin disease Inferred relationship Some
Autoimmune urticaria (disorder) Is a True Autoimmune skin disease Inferred relationship Some
Pemphigoid vegetans Is a False Autoimmune skin disease Inferred relationship Some
A rare superficial pemphigus disease characterised by severe intractable pruritus with erythematous or urticarial plaques and vesicles organised in a herpetiform pattern. Mucosae are generally spared. Eosinophilia in peripheral blood and low titres of circulating autoantibodies are observed in many cases. Histologically, minimal or no apparent acantholysis is associated. Is a True Autoimmune skin disease Inferred relationship Some
Erythema multiforme, dermal type Is a True Autoimmune skin disease Inferred relationship Some
Psoriasis of scalp (disorder) Is a True Autoimmune skin disease Inferred relationship Some
Transient neonatal epidermolysis bullosa acquisita (disorder) Is a False Autoimmune skin disease Inferred relationship Some
Rheumatoid arthritis with nailfold and finger-pulp infarcts (disorder) Is a True Autoimmune skin disease Inferred relationship Some
Rheumatoid neutrophilic dermatitis Is a True Autoimmune skin disease Inferred relationship Some
Rheumatoid arthritis with isolated nailfold vasculitis (disorder) Is a True Autoimmune skin disease Inferred relationship Some
Alopecia areata Is a True Autoimmune skin disease Inferred relationship Some
Autoimmune subepidermal bullous dermatosis (disorder) Is a True Autoimmune skin disease Inferred relationship Some
Erythema multiforme major (disorder) Is a True Autoimmune skin disease Inferred relationship Some
Erythema marginatum in acute rheumatic fever Is a True Autoimmune skin disease Inferred relationship Some
Pretibial pemphigoid (disorder) Is a True Autoimmune skin disease Inferred relationship Some
Localised scleroderma Is a True Autoimmune skin disease Inferred relationship Some
A very rare secondary neonatal autoimmune disease with characteristics of neonatal-onset of erythematous skin lesions with a linear appearance that gradually become indurated and hyperpigmented and progressively present skin atrophy. Positive serum antibodies (in particular antinuclear antibodies and/or rheumatoid factor) may be associated. Is a True Autoimmune skin disease Inferred relationship Some
Cutaneous atrophy due to rheumatoid arthritis (disorder) Is a True Autoimmune skin disease Inferred relationship Some

This concept is not in any reference sets

Back to Start