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Skin Diseases, Genetic
MeSH Descriptor Data 2025
Details
Qualifiers
MeSH Tree Structures
Concepts
MeSH Heading
Skin Diseases, Genetic
Tree Number(s)
C16.320.850
C17.800.827
Unique ID
D012873
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/D012873
Annotation
general or unspecified; prefer specifics
Scope Note
Diseases of the skin with a genetic component, usually the result of various inborn errors of metabolism.
Entry Version
SKIN DIS GENET
Entry Term(s)
Genetic Skin Diseases
NLM Classification #
WR 218
Previous Indexing
Skin Diseases (1975-1997)
Public MeSH Note
98
History Note
98; use explode 1970-97
Date Established
1998/01/01
Date of Entry
1999/01/01
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]
Genetic Diseases, Inborn [C16.320]
Adrenal Hyperplasia, Congenital [C16.320.033]
Alagille Syndrome [C16.320.051]
alpha 1-Antitrypsin Deficiency [C16.320.060]
Anemia, Hemolytic, Congenital [C16.320.070]
Anemia, Hypoplastic, Congenital [C16.320.077]
Ataxia Telangiectasia [C16.320.080]
Autoimmune Lymphoproliferative Syndrome [C16.320.089]
Blood Coagulation Disorders, Inherited [C16.320.099]
Brugada Syndrome [C16.320.100]
CADASIL [C16.320.129]
Camurati-Engelmann Syndrome [C16.320.144]
Cardiomyopathy, Hypertrophic, Familial [C16.320.160]
CHARGE Syndrome [C16.320.165]
Cherubism [C16.320.170]
Chromosome Disorders [C16.320.180]
Ciliopathies [C16.320.184]
Costello Syndrome [C16.320.188]
Cystic Fibrosis [C16.320.190]
Donohue Syndrome [C16.320.215]
Dwarfism [C16.320.240]
Eye Diseases, Hereditary [C16.320.290]
Familial Multiple Lipomatosis [C16.320.298]
Frasier Syndrome [C16.320.306]
GATA2 Deficiency [C16.320.314]
Genetic Diseases, X-Linked [C16.320.322]
Genetic Diseases, Y-Linked [C16.320.338]
Hajdu-Cheney Syndrome [C16.320.355]
Hemoglobinopathies [C16.320.365]
Hereditary Autoinflammatory Diseases [C16.320.382]
Heredodegenerative Disorders, Nervous System [C16.320.400]
Hyper-IgM Immunodeficiency Syndrome [C16.320.413]
Hyperthyroxinemia, Familial Dysalbuminemic [C16.320.427]
Imprinting Disorders [C16.320.447]
Kallmann Syndrome [C16.320.467]
Kartagener Syndrome [C16.320.480]
Laminopathies [C16.320.488]
Lennox Gastaut Syndrome [C16.320.495]
Loeys-Dietz Syndrome [C16.320.510]
Marfan Syndrome [C16.320.540]
Metabolism, Inborn Errors [C16.320.565]
Muscular Dystrophies [C16.320.577]
Myasthenic Syndromes, Congenital [C16.320.590]
Nail-Patella Syndrome [C16.320.600]
Neoplastic Syndromes, Hereditary [C16.320.700]
Oculocerebrorenal Syndrome [C16.320.709]
Orofaciodigital Syndromes [C16.320.714]
Osteoarthropathy, Primary Hypertrophic [C16.320.718]
Osteochondrodysplasias [C16.320.728]
Osteogenesis Imperfecta [C16.320.737]
Pain Insensitivity, Congenital [C16.320.775]
Pelger-Huet Anomaly [C16.320.784]
Primary Immunodeficiency Diseases [C16.320.798]
Pycnodysostosis [C16.320.812]
Renal Tubular Transport, Inborn Errors [C16.320.831]
Skin Diseases, Genetic [C16.320.850]
Albinism [C16.320.850.080]
Cutis Laxa [C16.320.850.180]
Darier Disease [C16.320.850.190]
Dermatitis, Atopic [C16.320.850.210]
Dyskeratosis Congenita [C16.320.850.235]
Ectodermal Dysplasia [C16.320.850.250]
Ehlers-Danlos Syndrome [C16.320.850.260]
Epidermolysis Bullosa [C16.320.850.275]
Erythrokeratodermia Variabilis [C16.320.850.337]
Hyaline Fibromatosis Syndrome [C16.320.850.368]
Ichthyosiform Erythroderma, Congenital [C16.320.850.400]
Ichthyosis Bullosa of Siemens [C16.320.850.402]
Ichthyosis Vulgaris [C16.320.850.405]
Ichthyosis, X-Linked [C16.320.850.408]
Incontinentia Pigmenti [C16.320.850.420]
Keratoderma, Palmoplantar [C16.320.850.475]
Leukokeratosis, Hereditary Mucosal [C16.320.850.542]
Lipoid Proteinosis of Urbach and Wiethe [C16.320.850.595]
Monilethrix [C16.320.850.647]
Netherton Syndrome [C16.320.850.673]
Pemphigus, Benign Familial [C16.320.850.700]
Porokeratosis [C16.320.850.730]
Porphyria, Erythropoietic [C16.320.850.738]
Porphyrias, Hepatic [C16.320.850.742]
Prolidase Deficiency [C16.320.850.746]
Pseudoxanthoma Elasticum [C16.320.850.750]
Rothmund-Thomson Syndrome [C16.320.850.765]
Sjogren-Larsson Syndrome [C16.320.850.820]
Trichothiodystrophy Syndromes [C16.320.850.895]
Xeroderma Pigmentosum [C16.320.850.970]
Werner Syndrome [C16.320.925]
Yellow Nail Syndrome [C16.320.962]
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]
Skin Diseases, Eczematous [C17.800.815]
Skin Diseases, Genetic [C17.800.827]
Albinism [C17.800.827.080]
Cutis Laxa [C17.800.827.180]
Darier Disease [C17.800.827.190]
Dermatitis, Atopic [C17.800.827.210]
Dyskeratosis Congenita [C17.800.827.235]
Ectodermal Dysplasia [C17.800.827.250]
Ehlers-Danlos Syndrome [C17.800.827.260]
Epidermolysis Bullosa [C17.800.827.275]
Erythrokeratodermia Variabilis [C17.800.827.337]
Hereditary Autoinflammatory Diseases [C17.800.827.368]
Hyaline Fibromatosis Syndrome [C17.800.827.384]
Ichthyosiform Erythroderma, Congenital [C17.800.827.400]
Ichthyosis Bullosa of Siemens [C17.800.827.403]
Ichthyosis Vulgaris [C17.800.827.405]
Ichthyosis, X-Linked [C17.800.827.408]
Incontinentia Pigmenti [C17.800.827.420]
Keratoderma, Palmoplantar [C17.800.827.475]
Leukokeratosis, Hereditary Mucosal [C17.800.827.595]
Monilethrix [C17.800.827.602]
Muir-Torre Syndrome [C17.800.827.610]
Netherton Syndrome [C17.800.827.655]
Pemphigus, Benign Familial [C17.800.827.700]
Porokeratosis [C17.800.827.730]
Porphyria, Erythropoietic [C17.800.827.738]
Porphyrias, Hepatic [C17.800.827.742]
Pseudoxanthoma Elasticum [C17.800.827.750]
Rothmund-Thomson Syndrome [C17.800.827.775]
Sjogren-Larsson Syndrome [C17.800.827.820]
Trichothiodystrophy Syndromes [C17.800.827.895]
Xeroderma Pigmentosum [C17.800.827.970]
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]
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Skin Diseases, Genetic
Preferred
Concept UI
M0019934
Scope Note
Diseases of the skin with a genetic component, usually the result of various inborn errors of metabolism.
Terms
Skin Diseases, Genetic
Preferred Term
Term UI
T037954
Date
01/01/1999
LexicalTag
NON
ThesaurusID
NLM (1966)
Genetic Skin Diseases
Term UI
T037953
Date
10/21/1996
LexicalTag
NON
ThesaurusID
NLM (1998)
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