Phenotypes for disease #02428 (RIEG3 (Axenfeld-Rieger syndrome, type 3 (RIEG-3)), OMIM:602482)

2 entries on 1 page. Showing entries 1 - 2.
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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     
0000275936 microphthalmia, anophthalmia, and coloboma; MIM, 602482 MIM, 602482 - Familial, autosomal dominant - - - - - LOVD 00382094
0000351560 Congenital heart defect, Patent foramen ovale, Atrial septal defect, congenital glaucoma - - Unknown - - - - - Juliana Mazzeu 00466173
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