OMIM-Bio2RDF-r3 (53,354)
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created at 2016-11-30 06:59:29 UTC
updated at 2016-11-30 09:55:54 UTC
OMIM in Bio2RDF r.3
Label
Id
10% due to paternal deletion http://bio2rdf.org/omim_resource:9c2bb3fff4ae482abda43e60a58bf7f7
11 pairs of ribs http://bio2rdf.org/omim_resource:ccc172cecd214062364fc86190d68ffb
11 rib pairs http://bio2rdf.org/omim_resource:dd22ab3d9b5f813c0db1ac71d195ab82
11 ribs http://bio2rdf.org/omim_resource:66159570caf390ecf9af11ba6e5030a4
12% due to epimutation http://bio2rdf.org/omim_resource:0d62c5d2b130cd0b36457338a5b6a4df
13 pairs of ribs http://bio2rdf.org/omim_resource:de9b0d2152b7e4ef86ff80c41de1c735
13 pairs of ribs (rare) http://bio2rdf.org/omim_resource:9f09a873e379a5748392ee62b78e1e7b
13 pairs of thoracic ribs http://bio2rdf.org/omim_resource:73bd3c27463607ca01190aa645b18798
13q- syndrome: family study. http://bio2rdf.org/pubmed:606176
13 ribs http://bio2rdf.org/omim_resource:d2fb7be54f643c74fff833d027608f1d
15% cases are familial http://bio2rdf.org/omim_resource:b61ec63a49ff256f5b43b6d7884ebe77
1,5-diaminopentanuria http://bio2rdf.org/omim_resource:d4c6ad502510c548196d5c2964bcc9f9
17-alpha-hydroxylase deficiency http://bio2rdf.org/omim_resource:a2fb1c5757f495f857953cd211bf5514
17-ketosteroid reductase defect http://bio2rdf.org/omim_resource:f68a9a4e4ff423139e41e8a9aa5140f8
1 in 17,000 in China http://bio2rdf.org/omim_resource:110abae6d3704eba0a8c65e2fbc139ab