From: <pr...@us...> - 2012-05-27 11:02:41
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Revision: 4322 http://obo.svn.sourceforge.net/obo/?rev=4322&view=rev Author: probins Date: 2012-05-27 11:02:34 +0000 (Sun, 27 May 2012) Log Message: ----------- Removing 610854 because it moved to 610682, which we already have Modified Paths: -------------- phenotype-commons/annotations/OMIM/by-disease/annotated/OMIM-166250.tab phenotype-commons/annotations/OMIM/by-disease/annotated/OMIM-602875.tab Removed Paths: ------------- phenotype-commons/annotations/OMIM/by-disease/annotated/OMIM-610854.tab Modified: phenotype-commons/annotations/OMIM/by-disease/annotated/OMIM-166250.tab =================================================================== --- phenotype-commons/annotations/OMIM/by-disease/annotated/OMIM-166250.tab 2012-05-27 09:27:47 UTC (rev 4321) +++ phenotype-commons/annotations/OMIM/by-disease/annotated/OMIM-166250.tab 2012-05-27 11:02:34 UTC (rev 4322) @@ -29,11 +29,12 @@ OMIM:166250 OSTEOGLOPHONIC DYSPLASIA HP:0002098 Respiratory distress IEA IEA OMIM:166250 HPO 17.02.2009 OMIM:166250 OSTEOGLOPHONIC DYSPLASIA HP:0002659 Increased susceptibility to fractures IEA IEA OMIM:166250 HPO 17.02.2009 OMIM:166250 OSTEOGLOPHONIC DYSPLASIA HP:0002676 Cloverleaf skull IEA IEA OMIM:166250 SKOEHLER 20.06.2010 -OMIM:166250 OSTEOGLOPHONIC DYSPLASIA HP:0003054 Short, bowed limbs IEA IEA OMIM:166250 HPO 17.02.2009 OMIM:166250 OSTEOGLOPHONIC DYSPLASIA HP:0003196 Short nose IEA IEA OMIM:166250 HPO 17.02.2009 OMIM:166250 OSTEOGLOPHONIC DYSPLASIA HP:0005864 Pseudoarthrosis IEA IEA OMIM:166250 HPO 17.02.2009 OMIM:166250 OSTEOGLOPHONIC DYSPLASIA HP:0006030 Short, wide phalanges IEA IEA OMIM:166250 HPO 17.02.2009 OMIM:166250 OSTEOGLOPHONIC DYSPLASIA HP:0006065 Short, broad metacarpals IEA IEA OMIM:166250 HPO 17.02.2009 OMIM:166250 OSTEOGLOPHONIC DYSPLASIA HP:0008905 Rhizomelic short stature IEA IEA OMIM:166250 HPO 17.02.2009 -OMIM:166250 OSTEOGLOPHONIC DYSPLASIA HP:0001783 Broad metatarsals TAS TAS OMIM:166250 probinson 08.05.2012 +OMIM:166250 OSTEOGLOPHONIC DYSPLASIA HP:0001783 Broad metatarsal TAS TAS OMIM:166250 probinson 08.05.2012 OMIM:166250 OSTEOGLOPHONIC DYSPLASIA HP:0010743 Short metatarsal bone TAS TAS OMIM:166250 probinson 08.05.2012 +OMIM:166250 OSTEOGLOPHONIC DYSPLASIA HP:0006487 Bowing of the long bones TAS TAS OMIM:166250 probinson 27.05.2012 +OMIM:166250 OSTEOGLOPHONIC DYSPLASIA HP:0009826 Hypoplasia involving bones of the extremities TAS TAS OMIM:166250 probinson 27.05.2012 Modified: phenotype-commons/annotations/OMIM/by-disease/annotated/OMIM-602875.tab =================================================================== --- phenotype-commons/annotations/OMIM/by-disease/annotated/OMIM-602875.tab 2012-05-27 09:27:47 UTC (rev 4321) +++ phenotype-commons/annotations/OMIM/by-disease/annotated/OMIM-602875.tab 2012-05-27 11:02:34 UTC (rev 4322) @@ -24,4 +24,4 @@ OMIM:602875 ACROMESOMELIC DYSPLASIA, MAROTEAUX TYPE HP:0008484 Narrow thoracolumbar interpediculate distance IEA IEA OMIM:602875 HPO 17.02.2009 OMIM:602875 ACROMESOMELIC DYSPLASIA, MAROTEAUX TYPE HP:0010230 Cone-shaped epiphyses of the phalanges of the hand IEA IEA OMIM:602875 HPO 17.02.2009 OMIM:602875 ACROMESOMELIC DYSPLASIA, MAROTEAUX TYPE HP:0010743 Short metatarsal bone TAS TAS OMIM:602875 probinson 08.05.2012 -OMIM:602875 ACROMESOMELIC DYSPLASIA, MAROTEAUX TYPE HP:0001783 Broad metatarsals TAS TAS OMIM:602875 probinson 08.05.2012 +OMIM:602875 ACROMESOMELIC DYSPLASIA, MAROTEAUX TYPE HP:0001783 Broad metatarsal TAS TAS OMIM:602875 probinson 08.05.2012 Deleted: phenotype-commons/annotations/OMIM/by-disease/annotated/OMIM-610854.tab =================================================================== --- phenotype-commons/annotations/OMIM/by-disease/annotated/OMIM-610854.tab 2012-05-27 09:27:47 UTC (rev 4321) +++ phenotype-commons/annotations/OMIM/by-disease/annotated/OMIM-610854.tab 2012-05-27 11:02:34 UTC (rev 4322) @@ -1,26 +0,0 @@ -Disease ID Disease Name Gene ID Gene Name Genotype Gene Symbol(s) Phenotype ID Phenotype Name Age of Onset ID Age of Onset Name Evidence ID Evidence Name Frequency Sex ID Sex Name Negation ID Negation Name Description Pub Assigned by Date Created -OMIM:610854 OSTEOGENESIS IMPERFECTA, TYPE IIB HP:0000007 Autosomal recessive inheritance IEA IEA OMIM:610854 HPO 17.02.2009 -OMIM:610854 OSTEOGENESIS IMPERFECTA, TYPE IIB HP:0000126 Hydronephrosis IEA IEA OMIM:610854 HPO 17.02.2009 -OMIM:610854 OSTEOGENESIS IMPERFECTA, TYPE IIB HP:0000260 Wide anterior fontanel IEA IEA OMIM:610854 HPO 17.02.2009 -OMIM:610854 OSTEOGENESIS IMPERFECTA, TYPE IIB HP:0000311 Round face IEA IEA OMIM:610854 HPO 17.02.2009 -OMIM:610854 OSTEOGENESIS IMPERFECTA, TYPE IIB HP:0000343 Long philtrum IEA IEA OMIM:610854 HPO 17.02.2009 -OMIM:610854 OSTEOGENESIS IMPERFECTA, TYPE IIB HP:0000520 Proptosis IEA IEA OMIM:610854 HPO 17.02.2009 -OMIM:610854 OSTEOGENESIS IMPERFECTA, TYPE IIB HP:0000592 Blue sclerae IEA IEA OMIM:610854 SKOEHLER 20.06.2010 -OMIM:610854 OSTEOGENESIS IMPERFECTA, TYPE IIB HP:0000767 Pectus excavatum IEA IEA OMIM:610854 HPO 17.02.2009 -OMIM:610854 OSTEOGENESIS IMPERFECTA, TYPE IIB HP:0000774 Narrow chest IEA IEA OMIM:610854 HPO 17.02.2009 -OMIM:610854 OSTEOGENESIS IMPERFECTA, TYPE IIB HP:0001522 Death in infancy ITM ITM OMIM:610854 HPO 17.02.2009 -OMIM:610854 OSTEOGENESIS IMPERFECTA, TYPE IIB HP:0002090 Pneumonia IEA IEA OMIM:610854 SKOEHLER 20.06.2010 -OMIM:610854 OSTEOGENESIS IMPERFECTA, TYPE IIB HP:0002093 Respiratory insufficiency ITM ITM OMIM:610854 HPO 17.02.2009 -OMIM:610854 OSTEOGENESIS IMPERFECTA, TYPE IIB HP:0002645 Wormian bones IEA IEA OMIM:610854 HPO 17.02.2009 -OMIM:610854 OSTEOGENESIS IMPERFECTA, TYPE IIB HP:0002757 Recurrent fractures ITM ITM OMIM:610854 HPO 17.02.2009 -OMIM:610854 OSTEOGENESIS IMPERFECTA, TYPE IIB HP:0002953 Vertebral compression fractures IEA IEA OMIM:610854 HPO 17.02.2009 -OMIM:610854 OSTEOGENESIS IMPERFECTA, TYPE IIB HP:0002968 Rhizomelic shortening IEA IEA OMIM:610854 HPO 17.02.2009 -OMIM:610854 OSTEOGENESIS IMPERFECTA, TYPE IIB HP:0002983 Micromelia IEA IEA OMIM:610854 HPO 17.02.2009 -OMIM:610854 OSTEOGENESIS IMPERFECTA, TYPE IIB HP:0003783 Externally rotated/abducted legs IEA IEA OMIM:610854 HPO 17.02.2009 -OMIM:610854 OSTEOGENESIS IMPERFECTA, TYPE IIB HP:0003784 Type 1 collagen overmodification IEA IEA OMIM:610854 HPO 17.02.2009 -OMIM:610854 OSTEOGENESIS IMPERFECTA, TYPE IIB HP:0003794 Open sutures IEA IEA OMIM:610854 HPO 17.02.2009 -OMIM:610854 OSTEOGENESIS IMPERFECTA, TYPE IIB HP:0004960 Absent pulmonary artery IEA IEA OMIM:610854 HPO 17.02.2009 -OMIM:610854 OSTEOGENESIS IMPERFECTA, TYPE IIB HP:0005304 Hypoplastic pulmonary veins IEA IEA OMIM:610854 HPO 17.02.2009 -OMIM:610854 OSTEOGENESIS IMPERFECTA, TYPE IIB HP:0005474 Decreased calvarial ossification IEA IEA OMIM:610854 HPO 17.02.2009 -OMIM:610854 OSTEOGENESIS IMPERFECTA, TYPE IIB HP:0005855 Multiple prenatal fractures IEA IEA OMIM:610854 HPO 17.02.2009 -OMIM:610854 OSTEOGENESIS IMPERFECTA, TYPE IIB HP:0006640 Multiple rib fractures IEA IEA OMIM:610854 HPO 17.02.2009 This was sent by the 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