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47 Possible Causes for LocusLink

  • Mosaic Trisomy 1

    The Human Genome, Chromosome 1 NCBI Locuslink for Chromosome 1 References Field LL, Tobias R, Robinson WP, Paisey R, Bain S. (1998) Maternal uniparental disomy of chromosome[mosaicism.bcchr.ca]

  • Faciocardiomusculoskeletal Syndrome Type Uruguay

    Locus-Specific Model Organisms MitoMap Phenotype Davis Human/Mouse Homology Maps Coriell The Jackson Laboratory Human Gene Nomenclature Human Genome Resources Genes and Disease LocusLink[fetal.com]

  • Ventriculomegaly with Defects of the Radius and Kidney

    Locus-Specific Model Organisms MitoMap Phenotype Davis Human/Mouse Homology Maps Coriell The Jackson Laboratory Human Gene Nomenclature Human Genome Resources Genes and Disease LocusLink[fetal.com]

  • Mesoaxial Synostotic Syndactyly with Phalangeal Reduction

    Locus-Specific Model Organisms MitoMap Phenotype Davis Human/Mouse Homology Maps Coriell The Jackson Laboratory Human Gene Nomenclature Human Genome Resources Genes and Disease LocusLink[fetal.com]

  • Faciocardiomelic Syndrome

    Locus-Specific Model Organisms MitoMap Phenotype Davis Human/Mouse Homology Maps Coriell The Jackson Laboratory Human Gene Nomenclature Human Genome Resources Genes and Disease LocusLink[fetal.com]

  • Antenatal Onset Minicore Myopathy with Arthrogryposis

    Locus-Specific Model Organisms MitoMap Phenotype Davis Human/Mouse Homology Maps Coriell The Jackson Laboratory Human Gene Nomenclature Human Genome Resources Genes and Disease LocusLink[fetal.com]

  • Autosomal Recessive Myeloproliferative Disease

    LocusLink: Hydroxymethylbilane synthase (HMBS); MIM number: 176000. OMIM: ‐post/Omim/dispmim?[els.net] LocusLink: Uroporphyrinogen decarboxylase (UROD); MIM number: 176100. OMIM: ‐post/Omim/dispmim?[els.net] LocusLink: Aminolevulinate, delta‐, synthase 2 (sideroblastic/hypochromic anemia) (ALAS2); MIM number: 301300. OMIM: ‐post/Omim/dispmim?[els.net]

  • Erythropoietic Coproporphyria

    LocusLink: Hydroxymethylbilane synthase (HMBS); MIM number: 176000. OMIM: ‐post/Omim/dispmim?[els.net] LocusLink: Uroporphyrinogen decarboxylase (UROD); MIM number: 176100. OMIM: ‐post/Omim/dispmim?[els.net] LocusLink: Aminolevulinate, delta‐, synthase 2 (sideroblastic/hypochromic anemia) (ALAS2); MIM number: 301300. OMIM: ‐post/Omim/dispmim?[els.net]

  • Cree Mental Retardation Syndrome

    Locus-Specific Model Organisms MitoMap Phenotype Davis Human/Mouse Homology Maps Coriell The Jackson Laboratory Human Gene Nomenclature Human Genome Resources Genes and Disease LocusLink[fetal.com]

  • Porphyria

    LocusLink: Hydroxymethylbilane synthase (HMBS); MIM number: 176000. OMIM: ‐post/Omim/dispmim?[els.net] LocusLink: Uroporphyrinogen decarboxylase (UROD); MIM number: 176100. OMIM: ‐post/Omim/dispmim?[els.net] LocusLink: Aminolevulinate, delta‐, synthase 2 (sideroblastic/hypochromic anemia) (ALAS2); MIM number: 301300. OMIM: ‐post/Omim/dispmim?[els.net]

Further symptoms