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    CTD Coats disease [ Homo sapiens (human) ]

    Gene ID: 1283, updated on 31-Aug-2024

    Summary

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    Official Symbol
    CTDprovided by HGNC
    Official Full Name
    Coats diseaseprovided by HGNC
    Primary source
    MIM:300216
    Gene type
    unknown
    Organism
    Homo sapiens
    Lineage
    Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo

    Bibliography

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    Related articles in PubMed

    1. Review: coats disease: the 2001 LuEsther T. Mertz lecture. Shields JA, et al. Retina, 2002 Feb. PMID 11884883
    2. Coats' disease of the retina (unilateral retinal telangiectasis) caused by somatic mutation in the NDP gene: a role for norrin in retinal angiogenesis. Black GC, et al. Hum Mol Genet, 1999 Oct. PMID 10484772

    GeneRIFs: Gene References Into Functions

    Phenotypes

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    Associated conditions

    Description Tests
    Coats disease
    OMIM: 300216GeneReviews: Not available

    General gene information

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    Property

    • phenotype only

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