Phenotypes for disease #02044 (Pyruvate carboxylase deficiency, OMIM:266150)

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     
0000060550 Pyruvate carboxylase deficiency (OMIM:266150) - - Familial, autosomal recessive - - - - - Daniel Trujillano 00080981
0000161618 see paper; ... pyruvate carboxylase deficency pyruvate carboxylase deficency Familial, autosomal recessive 03y - - - - Emanuele Coci 00213143
0000166525 see paper; ... pyruvate carboxylase deficiency pyruvate carboxylase deficiency Familial, autosomal recessive - - - - - Emanuele Coci 00218072
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