Phenotypes for disease #01721 (CHED (dystrophy, corneal, endothelial), OMIM:217700)

16 entries on 1 page. Showing entries 1 - 16.
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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     
0000154400 - - - - - - 7y - - LOVD 00206361
0000154401 - - - - - - 0y0m0d - - LOVD 00206362
0000154402 - - - - - - 0y0m0d - - LOVD 00206364
0000154403 - - - - - - 0y0m0d - - LOVD 00206365
0000154404 - - - - - - 0y0m0d - - LOVD 00206367
0000154405 - - - - - - 16y - - LOVD 00206368
0000154406 - - - - - - 0y0m0d - - LOVD 00206369
0000154407 - - - - - - 0y0m0d - - LOVD 00206370
0000154408 - - - - - - 5y - - LOVD 00206374
0000154412 - - - - - - 4y - - LOVD 00206385
0000154415 - - - - - - 0y0m0d - - LOVD 00206392
0000154416 - - - - - - 3y - - LOVD 00206393
0000154417 - - - - - - 0y0m0d - - LOVD 00206394
0000154420 - - - - - - 28y - - LOVD 00206399
0000154422 - - - - - - 0y0m0d - - LOVD 00206401
0000275969 retinal dystrophy; MIM, 216900 MIM, 216900 - Familial, autosomal recessive - - - - - LOVD 00382127
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