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http://purl.uniprot.org/diseases/1390http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Disease
http://purl.uniprot.org/diseases/1390http://www.w3.org/2000/01/rdf-schema#comment"An autosomal recessive developmental disorder characterized by a complex clinical phenotype with seemingly unrelated features involving multiple organs and systems. Developmental abnormalities include congenital cataracts and microcorneae, hypomyelination of the peripheral nervous system, impaired physical growth, delayed early motor and intellectual development, facial dysmorphism and hypogonadism. Central nervous system involvement, with cerebral and spinal cord atrophy, may be the result of disrupted development with superimposed degenerative changes. Affected individuals are prone to severe rhabdomyolysis after viral infections and to serious complications related to general anesthesia (such as pulmonary edema and epileptic seizures)."xsd:string
http://purl.uniprot.org/diseases/1390http://www.w3.org/2000/01/rdf-schema#seeAlsohttp://purl.uniprot.org/keywords/898
http://purl.uniprot.org/diseases/1390http://www.w3.org/2000/01/rdf-schema#seeAlsohttp://purl.uniprot.org/keywords/622
http://purl.uniprot.org/diseases/1390http://www.w3.org/2000/01/rdf-schema#seeAlsohttp://purl.uniprot.org/mim/604168
http://purl.uniprot.org/diseases/1390http://www.w3.org/2000/01/rdf-schema#seeAlsohttp://id.nlm.nih.gov/mesh/D000015
http://purl.uniprot.org/diseases/1390http://www.w3.org/2000/01/rdf-schema#seeAlsohttp://purl.uniprot.org/medgen/C1858726
http://purl.uniprot.org/diseases/1390http://www.w3.org/2004/02/skos/core#prefLabel"Congenital cataracts, facial dysmorphism, and neuropathy"xsd:string
http://purl.uniprot.org/diseases/1390http://purl.uniprot.org/core/mnemonic"CCFDN"xsd:string
http://purl.uniprot.org/uniprot/Q9Y5B0#SIPA99188516B509E41http://purl.uniprot.org/core/diseasehttp://purl.uniprot.org/diseases/1390
http://purl.uniprot.org/uniprot/#_F3C353205BA9AE68_up.disease_CCEDE49DE2E3EE29http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/diseases/1390