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http://purl.uniprot.org/diseases/3780http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Disease
http://purl.uniprot.org/diseases/3780http://www.w3.org/2000/01/rdf-schema#comment"A form of cardiofaciocutaneous syndrome, a multiple congenital anomaly disorder characterized by a distinctive facial appearance, heart defects and intellectual disability. Heart defects include pulmonic stenosis, atrial septal defects and hypertrophic cardiomyopathy. Some affected individuals present with ectodermal abnormalities such as sparse, friable hair, hyperkeratotic skin lesions and a generalized ichthyosis-like condition. Typical facial features are similar to Noonan syndrome. They include high forehead with bitemporal constriction, hypoplastic supraorbital ridges, downslanting palpebral fissures, a depressed nasal bridge, and posteriorly angulated ears with prominent helices. Distinctive features of CFC3 include macrostomia and horizontal shape of palpebral fissures."xsd:string
http://purl.uniprot.org/diseases/3780http://www.w3.org/2000/01/rdf-schema#seeAlsohttp://purl.uniprot.org/keywords/122
http://purl.uniprot.org/diseases/3780http://www.w3.org/2000/01/rdf-schema#seeAlsohttp://purl.uniprot.org/keywords/38
http://purl.uniprot.org/diseases/3780http://www.w3.org/2000/01/rdf-schema#seeAlsohttp://purl.uniprot.org/keywords/991
http://purl.uniprot.org/diseases/3780http://www.w3.org/2000/01/rdf-schema#seeAlsohttp://purl.uniprot.org/mim/615279
http://purl.uniprot.org/diseases/3780http://www.w3.org/2000/01/rdf-schema#seeAlsohttp://id.nlm.nih.gov/mesh/D004476
http://purl.uniprot.org/diseases/3780http://www.w3.org/2000/01/rdf-schema#seeAlsohttp://id.nlm.nih.gov/mesh/D006330
http://purl.uniprot.org/diseases/3780http://www.w3.org/2000/01/rdf-schema#seeAlsohttp://purl.uniprot.org/medgen/C3809006
http://purl.uniprot.org/diseases/3780http://www.w3.org/2000/01/rdf-schema#seeAlsohttp://purl.uniprot.org/medgen/CN176913
http://purl.uniprot.org/diseases/3780http://www.w3.org/2004/02/skos/core#prefLabel"Cardiofaciocutaneous syndrome 3"xsd:string
http://purl.uniprot.org/diseases/3780http://purl.uniprot.org/core/mnemonic"CFC3"xsd:string
http://purl.uniprot.org/uniprot/Q02750#SIP081266D633E0152Chttp://purl.uniprot.org/core/diseasehttp://purl.uniprot.org/diseases/3780
http://purl.uniprot.org/annotation/VAR_035093http://www.w3.org/2004/02/skos/core#relatedhttp://purl.uniprot.org/diseases/3780
http://purl.uniprot.org/annotation/VAR_035094http://www.w3.org/2004/02/skos/core#relatedhttp://purl.uniprot.org/diseases/3780
http://purl.uniprot.org/annotation/VAR_069780http://www.w3.org/2004/02/skos/core#relatedhttp://purl.uniprot.org/diseases/3780
http://purl.uniprot.org/uniprot/#_CFD0EF6F8C37437A_up.disease_EB91EDEE76E084DBhttp://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/diseases/3780