| 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 | | |
| 1 in 19,000 in Japan | http://bio2rdf.org/omim_resource:94c778f86f747c408f9755e551097904 | | |
| 1 in 50,000 in Korea | http://bio2rdf.org/omim_resource:84960a8b31a9b72e4bfc3e5021ec1c23 | | |
| (1) infantile nephropathic () | http://bio2rdf.org/omim_resource:b11fb5e207422ad034a3d1706f16ad65 | | |
| 20, 22 desmolase deficiency | http://bio2rdf.org/omim_resource:e99ea7f59ff2e3af26e800a4849c52b7 | | |
| 20-40% patients are asymptomatic | http://bio2rdf.org/omim_resource:4448152c94e2c453aeed221e2ce116a3 | | |
| 2:1 female preponderance | http://bio2rdf.org/omim_resource:25c16d8edb6b6e24265cbfcfe42477f8 | | |
| 21-hydroxylase deficiency | http://bio2rdf.org/omim_resource:384a16f6f4e8774e5e6e0f2dcde4f2b0 | | |
| 21-@HYDROXYLASE POLYMORPHISM | http://bio2rdf.org/omim_resource:613815_allele_4 | | |
| 21-@HYDROXYLASE POLYMORPHISM | http://bio2rdf.org/omim_resource:613815_allele_13 | | |
| 21-@HYDROXYLASE POLYMORPHISM | http://bio2rdf.org/omim_resource:613815_allele_12 | | |
| 22q13 deletion syndrome. | http://bio2rdf.org/pubmed:11391650 | | |
| 2-3 and 3-4 finger syndactyly | http://bio2rdf.org/omim_resource:3a52c472ad8e8edea4eab65128e24114 | | |
| 2-3% due to imprinting defects | http://bio2rdf.org/omim_resource:2ac162e4dbfc1786c8a546fb41d8d8a0 | | |
| 2-3 finger syndactyly | http://bio2rdf.org/omim_resource:90e2066205a72b9afa91a6a01b450e87 | | |
| 2-3 or 4-5 toe syndactyly | http://bio2rdf.org/omim_resource:fdc8c5bd501d460037d228c4bd3671b4 | | |