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7 Possible Causes for HOX7

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  • Facioscapulohumeral Muscular Dystrophy

    Sructure and sequence of the human homeobox gene HOX7. Genomics 11 , 670–678 (1991). 15 Langer, P.R., Waldrop, A.A. & Ward, D.C.[nature.com]

  • Yemenite Deaf Blind Hypopigmentation Syndrome

    , HYD1 4p16.1 Hypodontia, autosomal dominant, MSX1, HOX7, HYD1 4p16.1 Lipodystrophy, familial partial, with decreased subcutaneous fat of face and neck PPARGC1 4p15.1 Macular[addforums.com] Huntington disease HD, IT15 4p16.3 {Hypertension, essential, salt-sensitive} ADD1 4p16.3 Hypochondroplasia, 146000 FGFR3, ACH 4p16.3 Hypodontia with orofacial cleft, MSX1, HOX7[addforums.com] […] erythematosus, susceptibility to, 3} SLEB3 4p16-p15.2 Thanatophoric dysplasia, types I and II, FGFR3, ACH 4p16.3 Weyers acrodental dysostosis EVC 4p16 Witkop syndrome MSX1, HOX7[addforums.com]

  • Hypodontia - Dysplasia of Nails Syndrome

    Aliases for MSX1 Gene Msh Homeobox 1 2 3 5 Msh Homeobox 1-Like Protein 3 4 Homeobox Protein Hox-7 3 4 HOX7 3 4 Msh (Drosophila) Homeo Box Homolog 1 (Formerly Homeo Box 7)[genecards.org]

  • Congenital Non-Goitrous Hypothyroidism 6

    , MAX dimerization protein MLXIPL51085CHREBP, MIO, MONDOB, WBSCR14, WS-bHLH, bHLHd14MLX interacting protein-like MSC9242ABF-1, ABF1, MYOR, bHLHa22musculin MSX14487ECTD3, HOX7[grnpedia.org]

  • Partington Syndrome

    , MAX dimerization protein MLXIPL51085CHREBP, MIO, MONDOB, WBSCR14, WS-bHLH, bHLHd14MLX interacting protein-like MSC9242ABF-1, ABF1, MYOR, bHLHa22musculin MSX14487ECTD3, HOX7[grnpedia.org]

  • Familial Congenital Mirror Movements 2

    , MAX dimerization protein MLXIPL51085CHREBP, MIO, MONDOB, WBSCR14, WS-bHLH, bHLHd14MLX interacting protein-like MSC9242ABF-1, ABF1, MYOR, bHLHa22musculin MSX14487ECTD3, HOX7[grnpedia.org]

  • Ring Chromosome 4

    […] methylsterol oxidase) [DESP4] [ERG25] [SC4MOL] MSX1 4p16.1-p16.3 P28360 MSX1_HUMAN 142983 Homeobox protein MSX-1 (Homeobox protein Hox-7) (Msh homeobox 1-like protein) [HOX7[uniprot.org]

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