Skin Diseases, Genetic

Diseases of the skin with a genetic component, usually the result of various inborn errors of metabolism.

Year introduced: 1998

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Subheadings:

Restrict to MeSH Major Topic.

Do not include MeSH terms found below this term in the MeSH hierarchy.

Tree Number(s): C16.320.850, C17.800.827

MeSH Unique ID: D012873

Entry Terms:

• Genetic Skin Diseases
• Disease, Genetic Skin
• Diseases, Genetic Skin
• Genetic Skin Disease
• Skin Disease, Genetic

Previous Indexing:

• Skin Diseases (1975-1997)

All MeSH Categories
Diseases Category
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
Skin Diseases, Genetic
Albinism
Albinism, Ocular
Albinism, Oculocutaneous +
Piebaldism
Cutis Laxa
Darier Disease
Dermatitis, Atopic
Dyskeratosis Congenita
Ectodermal Dysplasia
Ectodermal Dysplasia 1, Anhidrotic
Ectodermal Dysplasia 3, Anhidrotic
Ectodermal Dysplasia, Hypohidrotic, Autosomal Recessive
Ellis-Van Creveld Syndrome
Focal Dermal Hypoplasia
Focal Facial Dermal Dysplasias
Neurocutaneous Syndromes
Pachyonychia Congenita +
Ehlers-Danlos Syndrome
Ehlers-Danlos Syndrome, Type IV
Epidermolysis Bullosa
Epidermolysis Bullosa Dystrophica
Epidermolysis Bullosa Simplex
Epidermolysis Bullosa, Junctional
Erythrokeratodermia Variabilis
Hyaline Fibromatosis Syndrome
Ichthyosiform Erythroderma, Congenital
Hyperkeratosis, Epidermolytic
Ichthyosis, Lamellar
Ichthyosis Bullosa of Siemens
Ichthyosis Vulgaris
Ichthyosis, X-Linked
Incontinentia Pigmenti
Keratoderma, Palmoplantar
Keratoderma, Palmoplantar, Diffuse +
Papillon-Lefevre Disease
Leukokeratosis, Hereditary Mucosal
Lipoid Proteinosis of Urbach and Wiethe
Monilethrix
Netherton Syndrome
Pemphigus, Benign Familial
Porokeratosis
Porphyria, Erythropoietic
Porphyrias, Hepatic
Coproporphyria, Hereditary
Porphyria Cutanea Tarda
Porphyria, Acute Intermittent
Porphyria, Hepatoerythropoietic
Porphyria, Variegate
Protoporphyria, Erythropoietic
Prolidase Deficiency
Pseudoxanthoma Elasticum
Rothmund-Thomson Syndrome
Sjogren-Larsson Syndrome
Trichothiodystrophy Syndromes
Xeroderma Pigmentosum

All MeSH Categories
Diseases Category
Skin and Connective Tissue Diseases
Skin Diseases
Skin Diseases, Genetic
Albinism
Albinism, Ocular
Albinism, Oculocutaneous +
Piebaldism
Cutis Laxa
Darier Disease
Dermatitis, Atopic
Dyskeratosis Congenita
Ectodermal Dysplasia
Ectodermal Dysplasia 1, Anhidrotic
Ectodermal Dysplasia 3, Anhidrotic
Ectodermal Dysplasia, Hypohidrotic, Autosomal Recessive
Ellis-Van Creveld Syndrome
Focal Dermal Hypoplasia
Focal Facial Dermal Dysplasias
Neurocutaneous Syndromes
Pachyonychia Congenita +
Ehlers-Danlos Syndrome
Ehlers-Danlos Syndrome, Type IV
Epidermolysis Bullosa
Epidermolysis Bullosa Acquisita
Epidermolysis Bullosa Dystrophica
Epidermolysis Bullosa Simplex
Epidermolysis Bullosa, Junctional
Erythrokeratodermia Variabilis
Hereditary Autoinflammatory Diseases
Behcet Syndrome
Cryopyrin-Associated Periodic Syndromes
Hyaline Fibromatosis Syndrome
Ichthyosiform Erythroderma, Congenital
Hyperkeratosis, Epidermolytic
Ichthyosis, Lamellar
Ichthyosis Bullosa of Siemens
Ichthyosis Vulgaris
Ichthyosis, X-Linked
Incontinentia Pigmenti
Keratoderma, Palmoplantar
Keratoderma, Palmoplantar, Diffuse +
Papillon-Lefevre Disease
Leukokeratosis, Hereditary Mucosal
Monilethrix
Muir-Torre Syndrome
Netherton Syndrome
Pemphigus, Benign Familial
Porokeratosis
Porphyria, Erythropoietic
Porphyrias, Hepatic
Coproporphyria, Hereditary
Porphyria Cutanea Tarda
Porphyria, Acute Intermittent
Porphyria, Hepatoerythropoietic
Porphyria, Variegate
Protoporphyria, Erythropoietic
Pseudoxanthoma Elasticum
Rothmund-Thomson Syndrome
Sjogren-Larsson Syndrome
Trichothiodystrophy Syndromes
Xeroderma Pigmentosum