Phenotypes for disease #02119 (MAHCF (aciduria, methylmalonic, and homocystinuria, cblF type (MAHCF)), OMIM:277380)

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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     
0000275692 Hyperchromia - - Familial, autosomal recessive - - - - - Juliana Mazzeu 00381850
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