Phenotypes for disease #02831 (LDS1 (Loeys-Dietz syndrome, type 1 (LDS-1)), OMIM:609192)

13 entries on 1 page. Showing entries 1 - 13.
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AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Protein     

Owner     

Individual ID     
0000117188 Pectus excavatum (HP:0000767), long fingers (HP:0100807), scoliosis (HP:0002650), high palate (HP:0000218), dural ectasia (HP:0100775), ascending aortic aneurysm (HP:0002631), carotid artery tortuosity (HP:0005302), no ectopia lentis (-HP:0001083), no hypertelorism (-HP:0000316), no bifid uvula (-HP:0000193) - - Familial, autosomal dominant - - 46y - - Norifumi Takeda 00144417
0000124328 Pectus excavatum (HP:0000767), long fingers (HP:0100807), scoliosis (HP:0002650), dural ectasia (HP:0100775), ascending aortic aneurysm (HP:0002631), hypertelorism (HP:0000316), bifid uvula (HP:0000193), Arterial tortuosity (HP:0005116), Tall stature (HP:0000098), Mitral valve prolapse (HP:0001634), no ectopia lentis (-HP:0001083) - - Isolated (sporadic) - - - - - Hironori Hara 00151836
0000185178 - - - Isolated (sporadic) - - - - - Marco Ritelli 00245208
0000185180 - - - Familial, autosomal dominant - - - - - Marco Ritelli 00245211
0000185181 - - - Isolated (sporadic) - - - - - Marco Ritelli 00245212
0000185183 - - - Familial, autosomal dominant - - - - - Marco Ritelli 00245213
0000185292 - - - Familial, autosomal dominant - - - - - Marco Ritelli 00245343
0000185294 - - - Isolated (sporadic) - - - - - Marco Ritelli 00245345
0000185295 - - - Isolated (sporadic) - - - - - Marco Ritelli 00245346
0000185296 - - - Isolated (sporadic) - - - - - Marco Ritelli 00245347
0000185297 - - - Familial, autosomal dominant - - - - - Marco Ritelli 00245348
0000268607 - - - Familial, autosomal dominant - - - - - Marco Ritelli 00373331
0000268608 - - - Isolated (sporadic) - - - - - Marco Ritelli 00373332
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