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    MROS Melkersson-Rosenthal syndrome [ Homo sapiens (human) ]

    Gene ID: 8011, updated on 2-Oct-2019

    Summary

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    Gene symbol
    MROS
    Gene description
    Melkersson-Rosenthal syndrome
    Primary source
    MIM:155900
    Gene type
    unknown
    Organism
    Homo sapiens
    Lineage
    Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
    Also known as
    MRS

    Genomic context

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    Location:
    9p11

    Bibliography

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    Related articles in PubMed

    1. [Melkersson-Rosenthal syndrome as a rare cause of recurrent facial nerve palsy]. Opala G, et al. Neurol Neurochir Pol, 2005 Jul-Aug. PMID 16096940
    2. Melkersson-Rosenthal syndrome: new clinicopathologic findings in 4 cases. Cockerham KP, et al. Arch Ophthalmol, 2000 Feb. PMID 10676788
    3. Melkersson-Rosenthal syndrome and de novo autosomal t(9;21)(p11;p11) translocation. Smeets E, et al. Clin Genet, 1994 Jun. PMID 7923865

    GeneRIFs: Gene References Into Functions

    Phenotypes

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    Melkersson-Rosenthal syndrome

    General gene information

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    Property

    • phenotype only

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