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    DFCTRPS Deafness, cataract, retinitis pigmentosa, and sperm abnormalities [ Homo sapiens (human) ]

    Gene ID: 100188774, updated on 7-Dec-2024

    Summary

    Gene symbol
    DFCTRPS
    Gene description
    Deafness, cataract, retinitis pigmentosa, and sperm abnormalities
    See related
    MIM:300719
    Gene type
    unknown
    Organism
    Homo sapiens
    Lineage
    Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo

    Phenotypes

    Deafness, cataract, retinitis pigmentosa, and sperm abnormalities