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36 relations: Afro-textured hair, Arrhythmogenic right ventricular dysplasia, Bullous impetigo, Corneodesmosin, Desmocollin, Desmoglein-1, Desmoglein-2, Desmoglein-3, Desmoglein-4, Desmoplakin, DSC2, Hair loss, Hypertrichosis simplex of the scalp, IgA pemphigus, Keratoderma, Lethal acantholytic epidermolysis bullosa, List of cutaneous conditions, List of genes mutated in cutaneous conditions, List of histologic stains that aid in diagnosis of cutaneous conditions, List of immunofluorescence findings for autoimmune bullous conditions, List of keratins expressed in the human integumentary system, List of target antigens in pemphigus, Monilethrix, Naxos syndrome, Palmoplantar keratoderma, Paraneoplastic pemphigus, Pemphigus erythematosus, Pemphigus foliaceus, Pemphigus vegetans, Pemphigus vulgaris, Plakoglobin, Plakophilin-1, Plakophilin-2, Skin fragility syndrome, Staphylococcal scalded skin syndrome, Stevens–Johnson syndrome.
Afro-textured hair
Afro-textured hair is the natural hair texture of certain populations in Africa, the African diaspora, Oceania and Asia.
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Arrhythmogenic right ventricular dysplasia
Arrhythmogenic right ventricular dysplasia (ARVD), or arrhythmogenic right ventricular cardiomyopathy (ARVC), is an inherited heart disease.
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Bullous impetigo
Bullous Impetigo is a skin condition that characteristically occurs in the newborn, and is caused by a bacterial infection, presenting with bullae.
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Corneodesmosin
Corneodesmosin is a protein that in humans is encoded by the CDSN gene.
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Desmocollin
Desmocollin is a type of cadherin.
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Desmoglein-1
Desmoglein-1 is a protein that in humans is encoded by the DSG1 gene.
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Desmoglein-2
Desmoglein-2 is a protein that in humans is encoded by the DSG2 gene.
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Desmoglein-3
Desmoglein-3 is a protein that in humans is encoded by the DSG3 gene.
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Desmoglein-4
Desmoglein-4 is a protein that in humans is encoded by the DSG4 gene.
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Desmoplakin
Desmoplakin is a protein in humans that is encoded by the DSP gene.
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DSC2
Desmocollin-2 is a protein that in humans is encoded by the DSC2 gene.
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Hair loss
Hair loss, also known as alopecia or baldness, refers to a loss of hair from part of the head or body.
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Hypertrichosis simplex of the scalp
Hypertrichosis simplex of the scalp is a cutaneous condition caused by defects in the corneodesmosin protein.
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IgA pemphigus
IgA pemphigus is a subtype of pemphigus with two distinct forms.
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Keratoderma
Keratoderma is a hornlike skin condition.
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Lethal acantholytic epidermolysis bullosa
Lethal acantholytic epidermolysis bullosa is a fatal genetic skin disorder caused by mutations in DSP.
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List of cutaneous conditions
Many conditions affect the human integumentary system—the organ system covering the entire surface of the body and composed of skin, hair, nails, and related muscle and glands.
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List of genes mutated in cutaneous conditions
A number of gene mutations have been linked to conditions of or affecting the human integumentary system.
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List of histologic stains that aid in diagnosis of cutaneous conditions
A number of histologic stains are used in the field of dermatology that aid in the diagnosis of conditions of or affecting the human integumentary system.
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List of immunofluorescence findings for autoimmune bullous conditions
Several cutaneous conditions can be diagnosed with the aid of immunofluorescence studies.
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List of keratins expressed in the human integumentary system
There are many different keratin proteins normally expressed in the human integumentary system.
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List of target antigens in pemphigus
Circulating auto-antibodies in the human body can target normal parts of the skin leading to disease.
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Monilethrix
Monilethrix (also referred to as beaded hair) is a rare autosomal dominant hair disease that results in short, fragile, broken hair that appears beaded.
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Naxos syndrome
Naxos disease (also known as "Diffuse non-epidermolytic palmoplantar keratoderma with woolly hair and cardiomyopathy," "Diffuse palmoplantar keratoderma with woolly hair and arrhythmogenic right ventricular cardiomyopathy firstly described in Naxos island by Dr Nikos Protonotarios," and "Naxos disease") is a cutaneous condition characterized by a palmoplantar keratoderma.
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Palmoplantar keratoderma
Palmoplantar keratodermas are a heterogeneous group of disorders characterized by abnormal thickening of the palms and soles.
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Paraneoplastic pemphigus
Paraneoplastic pemphigus is an autoimmune disorder stemming from an underlying tumor.
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Pemphigus erythematosus
Pemphigus erythematosus (also known as "Senear–Usher syndrome") is simply a localized form of pemphigus foliaceus with features of lupus erythematosus.
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Pemphigus foliaceus
Pemphigus foliaceus is an autoimmune blistering disease (bullous disorder) of the skin.
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Pemphigus vegetans
Pemphigus vegetans is a localized form of pemphigus vulgaris.
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Pemphigus vulgaris
Pemphigus vulgaris is a rare chronic blistering skin disease and the most common form of pemphigus.
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Plakoglobin
Plakoglobin, also known as junction plakoglobin or gamma-catenin, is a protein that in humans is encoded by the JUP gene.
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Plakophilin-1
Plakophilin-1 is a protein that in humans is encoded by the PKP1 gene.
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Plakophilin-2
Plakophilin-2 is a protein that in humans is encoded by the PKP2 gene.
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Skin fragility syndrome
Skin fragility syndrome (also known as "plakophilin 1 deficiency") is a cutaneous condition characterized by trauma-induced blisters and erosions.
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Staphylococcal scalded skin syndrome
Staphylococcal scalded skin syndrome (SSSS), also known as pemphigus neonatorum or Ritter's disease, or localized bullous impetigo is a dermatological condition caused by Staphylococcus aureus.
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Stevens–Johnson syndrome
Stevens–Johnson syndrome (SJS) is a type of severe skin reaction.
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