Phenotypes for disease #03417 (Hypermethioninemia with s-adenosylhomocysteine hydrolase deficiency, OMIM:613752)

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AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

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Age/Examination     

Age/Diagnosis     

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Protein     

Owner     

Individual ID     
0000060372 Hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase (OMIM:613752) - - Familial, autosomal recessive - - - - - Daniel Trujillano 00080803
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