Phenotypes for disease #01338 (FECD1 (dystrophy, corneal, Fuchs endothelial, type 1 (FECD-1)), OMIM:136800)

6 entries on 1 page. Showing entries 1 - 6.
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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     
0000154411 None - - - - - - - - LOVD 00206380
0000154413 - - - Familial, autosomal dominant - - - - - LOVD 00206387
0000154414 - - - Isolated (sporadic) - - - - - LOVD 00206391
0000154424 - - - Isolated (sporadic) - 46y - - - Soumittra Nagasamy 00206405
0000154425 - - - Isolated (sporadic) - 61y ? ? - Soumittra Nagasamy 00206408
0000154426 - - - Isolated (sporadic) - 69y - - - Soumittra Nagasamy 00206413
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