Phenotypes for disease #00339 (LRS (Larsen syndrome (LRS)), OMIM:150250)

25 entries on 1 page. Showing entries 1 - 25.
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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     
0000061315 - - - Unknown - - - - - Cynthia Silveira 00081548
0000186697 - - - Familial - - - - - Stephen Robertson 00247341
0000186698 - - - Familial - - - - - Stephen Robertson 00247342
0000186699 - - - Familial - - - - - Stephen Robertson 00247343
0000186702 - - - Familial - - - - - Stephen Robertson 00247352
0000186703 - - - Familial - - - - - Stephen Robertson 00247353
0000186716 - - - Familial - - - - - Stephen Robertson 00247399
0000186717 - - - Familial - - - - - Stephen Robertson 00247400
0000186718 - - - Familial - - - - - Stephen Robertson 00247401
0000186719 - - - Familial - - - - - Stephen Robertson 00247402
0000186720 - - - Familial - - - - - Stephen Robertson 00247403
0000186721 - - - Familial - - - - - Stephen Robertson 00247404
0000186722 - - - Familial - - - - - Stephen Robertson 00247405
0000186723 - - - Familial - - - - - Stephen Robertson 00247406
0000186724 - - - Familial - - - - - Stephen Robertson 00247407
0000186725 - - - Familial - - - - - Stephen Robertson 00247408
0000186726 - - - Familial - - - - - Stephen Robertson 00247409
0000186727 - - - Familial - - - - - Stephen Robertson 00247410
0000186728 - - - Familial - - - - - Stephen Robertson 00247411
0000186729 - - - Familial - - - - - Stephen Robertson 00247412
0000186730 - - - Familial - - - - - Stephen Robertson 00247413
0000186731 - - - Isolated (sporadic) - - - - - Nils Koelling 00247415
0000186742 - - - Familial - - - - - Stephen Robertson 00247463
0000186743 - - - Familial - - - - - Stephen Robertson 00247464
0000295561 congenital glaucoma, buphthalmos, palpebral edema, ecchymosis, corneal opacity, abnormality iris morphology, posterior vitreous detachment, Disproportionate short stature, hypotonia, patent foramen oval. posterior vitreous detachment Larsen syndrome Familial, autosomal recessive 00y01m - - abnormality iris morphology, buphthalmos - Miriam Erandi Reyna-Fabián 00402795
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