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1,089 Possible Causes for Epidermolysis Bullosa Simplex

  • Hereditary Renal Cell Carcinoma

    Molecular pathology of epidermolysis bullosa simplex Most cases of epidermolysis bullosa simplex are associated with mutations of the genes coding for keratins 5 and 14.[emedicine.medscape.com] Epidermolysis bullosa simplex Epidermolysis bullosa simplex (EBS) is the most common type of EB, accounting for about 70 percent of all cases.[epidermolysisbullosanews.com] What are the clinical features of epidermolysis bullosa? Epidermolysis bullosa simplex (EBS) For more details, see Epidermolysis bullosa simplex.[dermnetnz.org]

  • Epidermolysis Bullosa

    Can epidermolysis bullosa simplex be cured?[britishskinfoundation.org.uk] Type Locus & Gene OMIM Epidermolysis bullosa simplex with migratory circinate erythema 12q13 (KRT5) 609352 Epidermolysis bullosa simplex with mottled pigmentation.[en.wikipedia.org] GeneReview Scope Epidermolysis Bullosa Simplex: Included Phenotypes Epidermolysis bullosa simplex with mottled pigmentation (EBS-MP) Epidermolysis bullosa simplex, generalized[ncbi.nlm.nih.gov]

  • Dystrophic Epidermolysis Bullosa

    bullosa DDEB, dominant dystrophic epidermolysis bullosa DebRA, Dystrophic Epidermolysis Bullosa Research Association EBS, epidermolysis bullosa simplex HS-RDEB, Hallopeau[doi.org] 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] Molecular pathology of epidermolysis bullosa simplex Most cases of epidermolysis bullosa simplex are associated with mutations of the genes coding for keratins 5 and 14.[emedicine.medscape.com]

  • Epidermolysis Bullosa Simplex

    Epidermolysis Bullosa Simplex. 1998 Oct 7 [updated 2016 Oct 13].[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] bullosa simplex with migratory circinate erythema 12q13 ( KRT5 ) 609352 Epidermolysis bullosa simplex with mottled pigmentation.[en.wikipedia.org]

  • Junctional Epidermolysis Bullosa

    On DermNet NZ Epidermolysis bullosa Epidermolysis bullosa simplex Dystrophic epidermolysis bullosa Kindler syndrome Epidermolysis bullosa pruriginosa Epidermolysis bullosa[dermnetnz.org] bullosa acquisita epidermolysis bullosa dystrophica epidermolysis bullosa simplex Epidermolysis Bullosa with Deficiency of Galactosylhydroxylysyl Glucosyltransferase Epidermolysis[rgd.mcw.edu] bullosa simplex with hypodontia Epidermolysis bullosa simplex with mottled pigmentation Epidermolysis bullosa simplex with neuromuscular disease Epidermolysis bullosa simplex[icd9data.com]

  • Long QT Syndrome 1

    bullosa simplex with muscular dystrophy Epidermolysis bullosa simplex of Ogna plakophilin : Skin fragility syndrome Arrhythmogenic right ventricular dysplasia 9 centrosome[en.wikipedia.org] […] of Siemens ) KRT3 ( Meesmann juvenile epithelial corneal dystrophy ) KRT4 ( White sponge nevus ) KRT5 ( Epidermolysis bullosa simplex ) KRT8 ( Familial cirrhosis ) KRT10[en.wikipedia.org] ( Epidermolytic hyperkeratosis ) KRT12 ( Meesmann juvenile epithelial corneal dystrophy ) KRT13 ( White sponge nevus ) KRT14 ( Epidermolysis bullosa simplex ) KRT17 ( Steatocystoma[en.wikipedia.org]

  • Long QT Syndrome 5

    bullosa simplex with muscular dystrophy Epidermolysis bullosa simplex of Ogna plakophilin : Skin fragility syndrome Arrhythmogenic right ventricular dysplasia 9 centrosome[en.wikipedia.org] […] of Siemens ) KRT3 ( Meesmann juvenile epithelial corneal dystrophy ) KRT4 ( White sponge nevus ) KRT5 ( Epidermolysis bullosa simplex ) KRT8 ( Familial cirrhosis ) KRT10[en.wikipedia.org] ( Epidermolytic hyperkeratosis ) KRT12 ( Meesmann juvenile epithelial corneal dystrophy ) KRT13 ( White sponge nevus ) KRT14 ( Epidermolysis bullosa simplex ) KRT17 ( Steatocystoma[en.wikipedia.org]

  • Pachyonychia Congenita

    BACKGROUND: Painful foot blistering is a common problem in patients with epidermolysis bullosa simplex (EBS) and pachyonychia congenita (PC).[ncbi.nlm.nih.gov] bullosa simplex.[ncbi.nlm.nih.gov] A novel three-nucleotide deletion in the helix 2B region of keratin 14 in epidermolysis bullosa simplex: ΔE375. Hum. molec.[doi.org]

  • Deafness, Autosomal Dominant 23

    bullosa simplex with muscular dystrophy Epidermolysis bullosa simplex of Ogna plakophilin : Skin fragility syndrome Arrhythmogenic right ventricular dysplasia 9 centrosome[ipfs.io] bullosa simplex, Ogna type (O-EBS) [MIM: 131950 ] PLG P00747 non-pleiotropic Plasminogen deficiency (PLGD) [MIM: 217090 ] PLOD1 Q02809 non-pleiotropic Ehlers-Danlos syndrome[sbg.bio.ic.ac.uk] […] of Siemens ) KRT3 ( Meesmann juvenile epithelial corneal dystrophy ) KRT4 ( White sponge nevus ) KRT5 ( Epidermolysis bullosa simplex ) KRT8 ( Familial cirrhosis ) KRT10[ipfs.io]

  • Pretibial Dystrophic Epidermolysis Bullosa

    Molecular pathology of epidermolysis bullosa simplex Most cases of epidermolysis bullosa simplex are associated with mutations of the genes coding for keratins 5 and 14.[emedicine.medscape.com] Epidermolysis Bullosa Simplex A form of epidermolysis bullosa characterized by serous bullae that heal without scarring.[bioportfolio.com] What are the clinical features of epidermolysis bullosa? Epidermolysis bullosa simplex (EBS) For more details, see Epidermolysis bullosa simplex.[dermnetnz.org]

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