Phenotypes for disease #02915 (CTCRT-21;CCA-4 (cataract, type 21, multiple types (CTRCT-21, cataract, cerulean, congenital, type 4 (CCA-4))), OMIM:610202)

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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     
0000275989 congenital cataract; MIM, 610202 MIM, 610202 - Familial, autosomal dominant - - - - - LOVD 00382147
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