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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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