Phenotypes for disease #01722 (MCD (dystrophy, macular, corneal (MCD)), OMIM:217800)

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     
0000084437 Macular corneal dystrophy - - Familial, autosomal recessive - - - - - Hyojin Chae 00106630
0000084438 Macular corneal dystrophy - - Isolated (sporadic) - - - - - Hyojin Chae 00106631
0000084439 Macular corneal dystrophy - - Unknown - - - - - Hyojin Chae 00106632
0000084475 - - - Familial, autosomal recessive 50y - - - - Hyojin Chae 00106671
0000084476 - - - Familial, autosomal recessive 44y - - - - Hyojin Chae 00106672
0000084477 - - - Familial, autosomal recessive 35y - - - - Hyojin Chae 00106673
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