From: Chris M. <cmu...@us...> - 2007-07-20 01:25:43
|
Update of /cvsroot/obo/obo/ontology/phenotype/phenotype_xp In directory sc8-pr-cvs3.sourceforge.net:/tmp/cvs-serv16824 Added Files: omim_pheno_xp_fma-obol.obo Log Message: --- NEW FILE: omim_pheno_xp_fma-obol.obo --- ! parsing: OMIM_Pheno:10020 ! No parse for: OMIM_Pheno:10020 short stature (50%), prominent forehead, and coarse facies ! parsing: OMIM_Pheno:1003 ! No parse for: OMIM_Pheno:1003 lower limb hyperreflexia ! parsing: OMIM_Pheno:10031 ! No parse for: OMIM_Pheno:10031 forearm fullness ! parsing: OMIM_Pheno:1005 ! No parse for: OMIM_Pheno:1005 genetic heterogeneity (see 161400) ! parsing: OMIM_Pheno:10051 ! No parse for: OMIM_Pheno:10051 palatopharyngeal incompetence ! parsing: OMIM_Pheno:10082 ! No parse for: OMIM_Pheno:10082 tracheal calcifications ! parsing: OMIM_Pheno:10098 ! No parse for: OMIM_Pheno:10098 palatal rugosity ! parsing: OMIM_Pheno:10105 ! No parse for: OMIM_Pheno:10105 anterior peroneal weakness and atrophy ! parsing: OMIM_Pheno:10106 ! No parse for: OMIM_Pheno:10106 tibialis weakness and atrophy ! parsing: OMIM_Pheno:10109 [...5560 lines suppressed...] ! No parse for: OMIM_Pheno:22057 autosomal dominant (17q11.2) ! parsing: OMIM_Pheno:22065 ! No parse for: OMIM_Pheno:22065 autosomal dominant (8q11-q12) ! parsing: OMIM_Pheno:22068 ! No parse for: OMIM_Pheno:22068 chromosome translocation, t(8 ! parsing: OMIM_Pheno:22070 ! No parse for: OMIM_Pheno:22070 autosomal dominant (22q13.1) ! parsing: OMIM_Pheno:22072 ! No parse for: OMIM_Pheno:22072 chromosomal translocations involving 22q12 in most cases of ewing ! parsing: OMIM_Pheno:22074 ! No parse for: OMIM_Pheno:22074 autosomal dominant (15q26.1) ! parsing: OMIM_Pheno:22077 ! No parse for: OMIM_Pheno:22077 chromosome translocation t(15 ! parsing: OMIM_Pheno:22079 ! No parse for: OMIM_Pheno:22079 autosomal dominant (11p15.5-p15.1) ! parsing: OMIM_Pheno:22086 ! No parse for: OMIM_Pheno:22086 renal pelvic carcinoma ! parsing: OMIM_Pheno:22087 ! No parse for: OMIM_Pheno:22087 lung carcinoma ! parsing: OMIM_Pheno:22089 |