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1,984 Possible Causes for Caused by Mutation in the Laminin Gamma-2 Gene, Epidermolysis Bullosa, Syndactyly Does Not Occur

  • Herlitz Disease

    Mutations in genes coding for laminin-332 subunits (alpha-3 chain, laminin beta-3 chain, laminin gamma-2 chain), collagen XVII ( BP180 ), a6 integrin, and b4 integrin have[emedicine.medscape.com] What is Herlitz Junctional Epidermolysis Bullosa, LAMB3-related?[counsyl.com] Martin Carter Springer Science & Business Media , ٠٦‏/١٢‏/٢٠١٢ - 302 من الصفحات Because skin blisters are the initial manifestation of epidermolysis bullosa (EB), patients[books.google.com]

  • Hereditary Renal Cell Carcinoma

    Mutations in genes coding for laminin-332 subunits (alpha-3 chain, laminin beta-3 chain, laminin gamma-2 chain), collagen XVII (BP180), a6 integrin, and b4 integrin have been[emedicine.medscape.com] Dystrophic epidermolysis bullosa (DEB) is one of the major forms of epidermolysis bullosa.[ghr.nlm.nih.gov] On DermNet NZ Epidermolysis bullosa simplex Junctional epidermolysis bullosa Dystrophic epidermolysis bullosa Kindler syndrome Epidermolysis bullosa pruriginosa Epidermolysis[dermnetnz.org]

    Missing: Syndactyly Does Not Occur
  • Junctional Epidermolysis Bullosa

    Each gene encodes one of the three chains of heterotrimer laminin-332 proteins (including the alpha-3 chain, beta-3 chain and gamma-2-chain) responsible for the adherence[ncbi.nlm.nih.gov] bullosa (disorder) congenital junctional epidermolysis bullosa EBJ JEB Epidermolysis bullosa atrophicans Epidermolysis bullosa, junctional edit English junctional epidermolysis[wikidata.org] Mutations in genes coding for laminin-332 subunits (alpha-3 chain, laminin beta-3 chain, laminin gamma-2 chain), collagen XVII ( BP180 ), a6 integrin, and b4 integrin have[emedicine.medscape.com]

    Missing: Syndactyly Does Not Occur
  • Epidermolysis Bullosa

    Mutations in genes coding for laminin-332 subunits (alpha-3 chain, laminin beta-3 chain, laminin gamma-2 chain), collagen XVII ( BP180 ), a6 integrin, and b4 integrin have[emedicine.com] epidermolysis bullosa.[symptoma.com] Types Types of Epidermolysis Bullosa The different forms of epidermolysis bullosa include: Epidermolysis bullosa simplex —tissue separation and blistering occur in the top[niams.nih.gov]

    Missing: Syndactyly Does Not Occur
  • Epidermolysis Bullosa Simplex

    Mutations in genes coding for laminin-332 subunits (alpha-3 chain, laminin beta-3 chain, laminin gamma-2 chain), collagen XVII ( BP180 ), a6 integrin, and b4 integrin have[emedicine.com] Epidermolysis bullosa simplex is one of a group of genetic conditions called epidermolysis bullosa that cause the skin to be very fragile and to blister easily.[ghr.nlm.nih.gov] […] encoding keratin 5 or keratin 14 Epidermolysis bullosa simplex (disorder) Epidermolysis bullosa simplex Weber–Cockayne syndrome Statements Epidermolysis bullosa simplex Identifiers[wikidata.org]

    Missing: Syndactyly Does Not Occur
  • Dystrophic Epidermolysis Bullosa

    Mutations in genes coding for laminin-332 subunits (alpha-3 chain, laminin beta-3 chain, laminin gamma-2 chain), collagen XVII ( BP180 ), a6 integrin, and b4 integrin have[emedicine.medscape.com] Dystrophic epidermolysis bullosa (DEB) is one of the major forms of epidermolysis bullosa.[ghr.nlm.nih.gov] bullosa acquisita.There exist other types of inherited epidermolysis bullosa, junctional epidermolysis bullosa and epidermolysis bullosa simplex, which are not related to[en.wikipedia.org]

    Missing: Syndactyly Does Not Occur
  • Epidermolysis Bullosa Pruriginosa

    Mutations in genes coding for laminin-332 subunits (alpha-3 chain, laminin beta-3 chain, laminin gamma-2 chain), collagen XVII ( BP180 ), a6 integrin, and b4 integrin have[emedicine.medscape.com] Epidermolysis bullosa pruriginosa is a rare clinical subtype of dystrophic epidermolysis bullosa characterized by intense pruritus, secondary scratching-induced lesions, and[ncbi.nlm.nih.gov] Epidermolysis bullosa pruriginosa (EBP) is a rare subtype of dystrophic epidermolysis bullosa (DEB) characterized by intense pruritus, nodular or lichenoid lesions, and violaceous[ncbi.nlm.nih.gov]

    Missing: Syndactyly Does Not Occur
  • Pretibial Dystrophic Epidermolysis Bullosa

    Mutations in genes coding for laminin-332 subunits (alpha-3 chain, laminin beta-3 chain, laminin gamma-2 chain), collagen XVII ( BP180 ), a6 integrin, and b4 integrin have[emedicine.medscape.com] Abstract Pretibial epidermolysis bullosa is a rare variant of dystrophic epidermolysis bullosa, characterized by bullae and violaceous lichenoid papules and plaques of the[ncbi.nlm.nih.gov] Keywords: Collagen type VII, Epidermolysis bullosa dystrophica, Lichen planus INTRODUCTION Epidermolysis bullosa (EB) is a heterogenous group of mechano-bullous genetic disorders[ncbi.nlm.nih.gov]

    Missing: Syndactyly Does Not Occur
  • Epidermolysis Bullosa Simplex Type Cockayne-Touraine

    Mutations in genes coding for laminin 5 subunits (alpha-3 chain, laminin beta-3 chain, laminin gamma-2 chain), collagen XVII (BP180), a6 integrin, and b4 integrin have been[dermaamin.com] Prognosis - Epidermolysis bullosa simplex- Cockayne-Touraine type Not supplied. Treatment - Epidermolysis bullosa simplex- Cockayne-Touraine type Not supplied.[checkorphan.org] Martin Carter Springer Science & Business Media, ٠٦‏/١٢‏/٢٠١٢ - 302 من الصفحات Because skin blisters are the initial manifestation of epidermolysis bullosa (EB), patients[books.google.com]

    Missing: Syndactyly Does Not Occur
  • Epidermolysis Bullosa Simplex Type Kobner

    Mutations in genes coding for laminin-332 subunits (alpha-3 chain, laminin beta-3 chain, laminin gamma-2 chain), collagen XVII ( BP180 ), a6 integrin, and b4 integrin have[emedicine.medscape.com] epidermolysis epidermolysis epidermolysis bullosa epidermolysis bullosa epidermolysis bullosa epidermolysis bullosa Epidermolysis Bullosa Action Network Epidermolysis Bullosa[acronyms.thefreedictionary.com] Epidermolysis bullosa hereditaria.[dovemed.com]

    Missing: Syndactyly Does Not Occur

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