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Results 1 - 10 of 11 for Other genetic dermis disorder
  1. Progressive osseous heteroplasia 
    Progressive osseous heteroplasia is a disorder in which bone forms within skin and muscle tissue. Bone that forms outside the skeleton is called heterotopic or ectopic ...
    https://medlineplus.gov/.../progressive-osseous-heteroplasia - Genetics
  2. Junctional epidermolysis bullosa 
    ... Testing Registry: Junctional epidermolysis bullosa gravis of Herlitz Genetic Testing Registry: Junctional epidermolysis ... ClinicalTrials.gov EPIDERMOLYSIS BULLOSA, JUNCTIONAL 1A, INTERMEDIATE; ...
    https://medlineplus.gov/.../junctional-epidermolysis-bullosa - Genetics
  3. LAMC2 gene 
    The LAMC2 gene provides instructions for making one part (subunit) of a protein called laminin 332 (formerly known as laminin 5). This protein is made up of ...
    https://medlineplus.gov/genetics/gene/lamc2 - Genetics
  4. COL17A1 gene 
    The COL17A1 gene provides instructions for making a protein that is used to assemble type XVII collagen. Collagens are a family of proteins that strengthen ...
    https://medlineplus.gov/genetics/gene/col17a1 - Genetics
  5. LAMB3 gene 
    The LAMB3 gene provides instructions for making one part (subunit) of a protein called laminin 332 (formerly known as laminin 5). This protein is made up of ...
    https://medlineplus.gov/genetics/gene/lamb3 - Genetics
  6. LAMA3 gene 
    The LAMA3 gene provides instructions for making one part (subunit) of a protein called laminin 332 (formerly known as laminin 5). This protein is made up of ...
    https://medlineplus.gov/genetics/gene/lama3 - Genetics
  7. Dystrophic epidermolysis bullosa 
    ... epidermolysis bullosa Genetic Testing Registry: Epidermolysis bullosa dystrophica Genetic Testing Registry: Recessive ... ClinicalTrials.gov EPIDERMOLYSIS BULLOSA DYSTROPHICA, AUTOSOMAL DOMINANT; ...
    https://medlineplus.gov/.../dystrophic-epidermolysis-bullosa - Genetics
  8. Primary localized cutaneous amyloidosis 
    ... to be related conditions that arise through similar disease mechanisms. The genetic basis of nodular amyloidosis is unknown.The OSMR ... Genetic Testing Registry: Amyloidosis, primary localized cutaneous, 2 Genetic Testing Registry: Amyloidosis, primary localized ... ClinicalTrials.gov AMYLOIDOSIS, PRIMARY LOCALIZED CUTANEOUS, 1; ...
    https://medlineplus.gov/.../primary-localized-cutaneous-amyloidosis - Genetics
  9. Kindler epidermolysis bullosa 
    ... Kindler syndrome Kindler's syndrome Poikiloderma of Kindler Genetic Testing Registry: Kindler syndrome Kindler epidermolysis bullosa National Organization for Rare Disorders (NORD) KINDLER SYNDROME; KNDLRS PubMed Ashton GH, McLean ...
    https://medlineplus.gov/.../condition/kindler-epidermolysis-bullosa - Genetics
  10. FERMT1 gene 
    ... in people with Kindler epidermolysis bullosa (EB). This disorder is a rare type of epidermolysis bullosa, which is a group of genetic conditions that cause the skin to be very ...
    https://medlineplus.gov/genetics/gene/fermt1 - Genetics
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