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322 Possible Causes for Xiphotheca, tecta

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  • Deafness, Autosomal Dominant 23

    MYO3A, MYO6, MYO7A, NLRP3, OTOA, OTOF, OTOG, P2RX2, PCDH15, PNPT1, POU3F4, POU4F3, PRPS1, PTPRQ, RAI1, RDX, SERPINB6, SIX1, SLC17A8, SMPX, SLC26A4, SLC26A5, STRC, TBC1D24, TECTA[bredagenetics.com] POU4F3, PRPS1, PTPRQ, RDX, S1PR2, SALL1, SEMA3E, SERPINB6, SIX1, SIX5, SLC17A8, SLC19A2, SLC26A4, SLC26A5, SLITRK6, SMPX, SNAI2, SOX10, SPATA5, STRC, SYNE4, TBC1D24, TCOF1, TECTA[cegat.de] Mutations in the ACTG1 , CDH23 , CLDN14 , COCH , COL11A2 , DFNA5 , ESPN , EYA4 , GJB2 , GJB6 , KCNQ4 , MYO15A , MYO6 , MYO7A , OTOF , PCDH15 , POU3F4 , SLC26A4 , STRC , TECTA[ipfs.io]

    Missing: Xiphotheca
  • Mitochondrial Non-Syndromic Sensorineural Deafness

    MYO3A, MYO6, MYO7A, NLRP3, OTOA, OTOF, OTOG, P2RX2, PCDH15, PNPT1, POU3F4, POU4F3, PRPS1, PTPRQ, RAI1, RDX, SERPINB6, SIX1, SLC17A8, SMPX, SLC26A4, SLC26A5, STRC, TBC1D24, TECTA[bredagenetics.com] KCNJ10, LHFPL5, LOXHD1, LRTOMT, MARVELD2, MSRB3, MYO15A, MYO3A, MYO6, MYO7A, OTOA, OTOF, PCDH15, POU3F4, PRPS1, PTPRQ, RDX, SERPINB6, SLC12A1, SLC26A4, SLC26A5, SMPX, STRC, TECTA[centogene.com] CLDN14 , COCH , COL11A2 , DFNA5 , DFNB31 , DFNB59 , ESPN , EYA4 , GJB2 , GJB6 , KCNQ4 , LHFPL5 , MT-TS1 , MYO15A , MYO6 , MYO7A , OTOF , PCDH15 , POU3F4 , SLC26A4 , STRC , TECTA[ourmed.org]

    Missing: Xiphotheca
  • Autosomal Recessive Deafness 42

    KCNJ10, LHFPL5, LOXHD1, LRTOMT, MARVELD2, MSRB3, MYO15A, MYO3A, MYO6, MYO7A, OTOA, OTOF, PCDH15, POU3F4, PRPS1, PTPRQ, RDX, SERPINB6, SLC12A1, SLC26A4, SLC26A5, SMPX, STRC, TECTA[centogene.com] Knobloch syndrome Laminin Junctional epidermolysis bullosa Laryngoonychocutaneous syndrome Other Congenital stromal corneal dystrophy Raine syndrome Urbach–Wiethe disease TECTA[en.wikipedia.org] DFNA8/12 caused by TECTA mutations is the most identified subtype of nonsyndromic autosomal dominant hearing loss.[ghr.nlm.nih.gov]

    Missing: Xiphotheca
  • X-Linked Non-Syndromic Sensorineural Deafness Type DFN

    MYO3A, MYO6, MYO7A, NLRP3, OTOA, OTOF, OTOG, P2RX2, PCDH15, PNPT1, POU3F4, POU4F3, PRPS1, PTPRQ, RAI1, RDX, SERPINB6, SIX1, SLC17A8, SMPX, SLC26A4, SLC26A5, STRC, TBC1D24, TECTA[bredagenetics.com] In families with autosomal dominant HL in the midfrequencies starting before the age of 10 years, the TECTA gene might be analyzed (Tables 1 and 2). • DFNB: Although more[studyres.com] CLDN14 , COCH , COL11A2 , DFNA5 , DFNB31 , DFNB59 , ESPN , EYA4 , GJB2 , GJB6 , KCNQ4 , LHFPL5 , MT-TS1 , MYO15A , MYO6 , MYO7A , OTOF , PCDH15 , POU3F4 , SLC26A4 , STRC , TECTA[ourmed.org]

    Missing: Xiphotheca
  • Autosomal Dominant Deafness 28

    No mutations were discovered in the TECTA gene.[research.library.mun.ca] […] profound;stable DFNB12 CDH23 Prelingual Severe to profound; stable DFNB16 STRC Prelingual Severe to profound; stable DFNB18 USH1C Prelingual Severe to profound; stable DFNB21 TECTA[iccons.co.in] Knobloch syndrome Laminin Junctional epidermolysis bullosa Laryngoonychocutaneous syndrome Other Congenital stromal corneal dystrophy Raine syndrome Urbach–Wiethe disease TECTA[en.wikipedia.org]

    Missing: Xiphotheca
  • Autosomal Dominant Deafness 11

    MYO3A, MYO6, MYO7A, NLRP3, OTOA, OTOF, OTOG, P2RX2, PCDH15, PNPT1, POU3F4, POU4F3, PRPS1, PTPRQ, RAI1, RDX, SERPINB6, SIX1, SLC17A8, SMPX, SLC26A4, SLC26A5, STRC, TBC1D24, TECTA[bredagenetics.com] Mutations in the ACTG1 , CDH23 , CLDN14 , COCH , COL11A2 , DFNA5 , ESPN , EYA4 , GJB2 , GJB6 , KCNQ4 , MYO15A , MYO6 , MYO7A , OTOF , PCDH15 , POU3F4 , SLC26A4 , STRC , TECTA[ipfs.io] Knobloch syndrome Laminin Junctional epidermolysis bullosa Laryngoonychocutaneous syndrome Other Congenital stromal corneal dystrophy Raine syndrome Urbach–Wiethe disease TECTA[en.wikipedia.org]

    Missing: Xiphotheca
  • Non-Syndromic Tibial Hemimelia

    Revista Brasileira de Otorrinolaringologia 74 (5), 786-789 , 2008 11 2008 Aberrant transcript produced by a splice donor site deletion in the TECTA gene is associated with[scholar.google.de]

    Missing: Xiphotheca
  • Schmid Metaphyseal Chondrodysplasia

    Knobloch syndrome Laminin Junctional epidermolysis bullosa Laryngoonychocutaneous syndrome Other Congenital stromal corneal dystrophy Raine syndrome Urbach–Wiethe disease TECTA[en.wikipedia.org] Bullous pemphigoid Laminin Junctional epidermolysis bullosa Laryngoonychocutaneous syndrome Other Congenital stromal corneal dystrophy Raine syndrome Urbach–Wiethe disease TECTA[infogalactic.com]

    Missing: Xiphotheca
  • Autosomal Recessive Deafness 1B

    MYO3A, MYO6, MYO7A, NLRP3, OTOA, OTOF, OTOG, P2RX2, PCDH15, PNPT1, POU3F4, POU4F3, PRPS1, PTPRQ, RAI1, RDX, SERPINB6, SIX1, SLC17A8, SMPX, SLC26A4, SLC26A5, STRC, TBC1D24, TECTA[bredagenetics.com] KCNJ10, LHFPL5, LOXHD1, LRTOMT, MARVELD2, MSRB3, MYO15A, MYO3A, MYO6, MYO7A, OTOA, OTOF, PCDH15, POU3F4, PRPS1, PTPRQ, RDX, SERPINB6, SLC12A1, SLC26A4, SLC26A5, SMPX, STRC, TECTA[centogene.com] Knobloch syndrome Laminin Junctional epidermolysis bullosa Laryngoonychocutaneous syndrome Other Congenital stromal corneal dystrophy Raine syndrome Urbach–Wiethe disease TECTA[en.wikipedia.org]

    Missing: Xiphotheca
  • Rhizomelic Syndrome Type Urbach

    Bullous pemphigoid Laminin Junctional epidermolysis bullosa Laryngoonychocutaneous syndrome Other Congenital stromal corneal dystrophy Raine syndrome Urbach–Wiethe disease TECTA[ipfs.io] Knobloch syndrome Laminin Junctional epidermolysis bullosa Laryngoonychocutaneous syndrome Other Congenital stromal corneal dystrophy Raine syndrome Urbach–Wiethe disease TECTA[en.wikipedia.org]

    Missing: Xiphotheca

Further symptoms