Phenotypes for disease #01076 (Alport syndrome, mental retardation, midface hypoplasia, and elliptocytosis)

3 entries on 1 page. Showing entries 1 - 3.
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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     
0000166545 Alport Syndrom X-linked recessive moderate hearing loss / hematuria alport syndrome Familial, X-linked 17y - - - - Viviana Karina Dalamón 00218099
0000185625 Persistent microhaematuria, proteinuria, astigmatism and myopia. - - Familial, autosomal dominant - - - - - Alessandra Renieri 00245757
0000185628 Persistent microhaematuria, absent proteinuria. Normal audiological and ophthalmoscopic evaluation - - Familial, X-linked - - - - - Alessandra Renieri 00245760
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