cerebroretinal microangiopathy with calcifications and cysts Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Coats plus syndrome is a pleiotropic multisystem disorder characterized by retinal telangiectasia and exudates, intracranial calcification with leukoencephalopathy and brain cysts, osteopenia with predisposition to fractures, bone marrow suppression, gastrointestinal bleeding and portal hypertension. It is transmitted as an autosomal recessive disease. (Orphanet Rare Disease Ontology, Orphanet_313838)
External Link http://www.omim.org/entry/612199
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Genes

1 genes associated with the cerebroretinal microangiopathy with calcifications and cysts phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
CTC1 CTS telomere maintenance complex component 1