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Genetic genealogy / Congenital disorders / Spondyloepimetaphyseal dysplasia / Rare diseases / Spondyloepiphyseal dysplasia congenita / Osteochondrodysplasia / Dysplasia / Pseudoachondroplasia / Multiple epiphyseal dysplasia / Health / Medicine / Collagen disease


The Orphanet Rare Diseases Ontology (ORDO) : a reference tool integrating clinical and genetic data. A. Rath*, A. Olry*, C. Gonthier*, L. Chanas*, H. Parkinson**, J. Malone**, D. Vasant**, M. Hanauer*, B. Urbero*, S. Ay
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Document Date: 2014-05-02 11:54:43

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File Size: 1,88 MB

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City

Paris / /

Country

France / /

Facility

European Bioinformatics Institute / /

IndustryTerm

reference tool / de services / /

Organization

European Bioinformatics Institute / Ontology Lookup Service / /

Person

JO QMBUGPSNT / JO UIF OFBS GVUVSF / JO DMJOJDBM EBUBCBTFT / JO VTF METHODOLOGY / /

ProgrammingLanguage

XML / /

Technology

XML / RDF / GPS / /

URL

www.orphadata.org / www.orpha.net / /

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