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Skin Abnormalities
MeSH Descriptor Data 2024
Details
Qualifiers
MeSH Tree Structures
Concepts
MeSH Heading
Skin Abnormalities
Tree Number(s)
C16.131.831
C17.800.804
Unique ID
D012868
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/D012868
Annotation
for congenital structural abnormalities only; general or unspecified; prefer specifics
Scope Note
Congenital structural abnormalities of the skin.
Entry Version
SKIN ABNORM
Entry Term(s)
Abnormalities, Skin
NLM Classification #
WR 218
Previous Indexing
Skin/abnormalities (1966-1997)
Public MeSH Note
98
History Note
98; use explode 1985-97
Date Established
1998/01/01
Date of Entry
1984/05/02
Revision Date
2019/05/24
Allowable Qualifiers
blood (BL)
cerebrospinal fluid (CF)
chemically induced (CI)
classification (CL)
complications (CO)
diagnosis (DI)
diagnostic imaging (DG)
diet therapy (DH)
drug therapy (DT)
economics (EC)
embryology (EM)
enzymology (EN)
epidemiology (EP)
ethnology (EH)
etiology (ET)
genetics (GE)
history (HI)
immunology (IM)
metabolism (ME)
microbiology (MI)
mortality (MO)
nursing (NU)
parasitology (PS)
pathology (PA)
physiopathology (PP)
prevention & control (PC)
psychology (PX)
radiotherapy (RT)
rehabilitation (RH)
surgery (SU)
therapy (TH)
urine (UR)
veterinary (VE)
virology (VI)
Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
Congenital Abnormalities [C16.131]
Abnormalities, Drug-Induced [C16.131.042]
Abnormalities, Multiple [C16.131.077]
Abnormalities, Radiation-Induced [C16.131.080]
Abnormalities, Severe Teratoid [C16.131.085]
Aicardi Syndrome [C16.131.162]
Cardiovascular Abnormalities [C16.131.240]
Chromosome Disorders [C16.131.260]
Congenital Microtia [C16.131.287]
Digestive System Abnormalities [C16.131.314]
Eye Abnormalities [C16.131.384]
Hernias, Diaphragmatic, Congenital [C16.131.433]
Lymphatic Abnormalities [C16.131.482]
Musculoskeletal Abnormalities [C16.131.621]
Nervous System Malformations [C16.131.666]
Respiratory System Abnormalities [C16.131.740]
Situs Inversus [C16.131.810]
Skin Abnormalities [C16.131.831]
Acrodermatitis [C16.131.831.066]
Carney Complex [C16.131.831.108]
Dyskeratosis Congenita [C16.131.831.150]
Ectodermal Dysplasia [C16.131.831.350]
Ehlers-Danlos Syndrome [C16.131.831.428]
Epidermolysis Bullosa [C16.131.831.493]
Ichthyosis [C16.131.831.512]
Incontinentia Pigmenti [C16.131.831.580]
Port-Wine Stain [C16.131.831.675]
Prolidase Deficiency [C16.131.831.720]
Pseudoxanthoma Elasticum [C16.131.831.766]
Rothmund-Thomson Syndrome [C16.131.831.775]
Sclerema Neonatorum [C16.131.831.812]
Trichothiodystrophy Syndromes [C16.131.831.874]
Xeroderma Pigmentosum [C16.131.831.936]
Stomatognathic System Abnormalities [C16.131.850]
Thyroid Dysgenesis [C16.131.894]
Urogenital Abnormalities [C16.131.939]
Skin and Connective Tissue Diseases [C17]
Skin Diseases [C17.800]
Acneiform Eruptions [C17.800.030]
Angiolymphoid Hyperplasia with Eosinophilia [C17.800.060]
Breast Diseases [C17.800.090]
Calcinosis Cutis [C17.800.113]
Cutaneous Fistula [C17.800.135]
Dermatitis [C17.800.174]
Dermatomyositis [C17.800.185]
Erythema [C17.800.229]
Exanthema [C17.800.257]
Facial Dermatoses [C17.800.271]
Foot Diseases [C17.800.321]
Hair Diseases [C17.800.329]
Hand Dermatoses [C17.800.338]
Keratoacanthoma [C17.800.417]
Keratosis [C17.800.428]
Leg Dermatoses [C17.800.446]
Lipomatosis [C17.800.463]
Lupus Erythematosus, Cutaneous [C17.800.480]
Morgellons Disease [C17.800.518]
Nail Diseases [C17.800.529]
Necrobiotic Disorders [C17.800.550]
Necrolytic Migratory Erythema [C17.800.551]
Nephrogenic Fibrosing Dermopathy [C17.800.553]
Panniculitis [C17.800.566]
Photosensitivity Disorders [C17.800.600]
Pigmentation Disorders [C17.800.621]
Prurigo [C17.800.674]
Pruritus [C17.800.685]
Pyoderma [C17.800.695]
Rosacea [C17.800.716]
Scalp Dermatoses [C17.800.738]
Scleredema Adultorum [C17.800.751]
Scleroderma, Localized [C17.800.767]
Scleroderma, Systemic [C17.800.784]
Sebaceous Gland Diseases [C17.800.794]
Skin Abnormalities [C17.800.804]
Acrodermatitis [C17.800.804.066]
Anetoderma [C17.800.804.108]
Dyskeratosis Congenita [C17.800.804.150]
Ectodermal Dysplasia [C17.800.804.350]
Ehlers-Danlos Syndrome [C17.800.804.428]
Epidermolysis Bullosa [C17.800.804.493]
Ichthyosis [C17.800.804.512]
Incontinentia Pigmenti [C17.800.804.580]
Port-Wine Stain [C17.800.804.675]
Pseudoxanthoma Elasticum [C17.800.804.766]
Rothmund-Thomson Syndrome [C17.800.804.775]
Sclerema Neonatorum [C17.800.804.812]
Trichothiodystrophy Syndromes [C17.800.804.874]
Xeroderma Pigmentosum [C17.800.804.936]
Skin Diseases, Eczematous [C17.800.815]
Skin Diseases, Genetic [C17.800.827]
Skin Diseases, Infectious [C17.800.838]
Skin Diseases, Metabolic [C17.800.849]
Skin Diseases, Papulosquamous [C17.800.859]
Skin Diseases, Vascular [C17.800.862]
Skin Diseases, Vesiculobullous [C17.800.865]
Skin Neoplasms [C17.800.882]
Skin Ulcer [C17.800.893]
Sweat Gland Diseases [C17.800.946]
Xanthogranuloma, Juvenile [C17.800.973]
Expand All
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Skin Abnormalities
Preferred
Concept UI
M0019926
Scope Note
Congenital structural abnormalities of the skin.
Terms
Skin Abnormalities
Preferred Term
Term UI
T037935
Date
01/01/1999
LexicalTag
NON
ThesaurusID
NLM (1985)
Abnormalities, Skin
Term UI
T037934
Date
02/20/1997
LexicalTag
NON
ThesaurusID
NLM (1998)
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