Phenotype #0000161616

Individual ID 00213141
Associated disease -
Phenotype details see paper; ...
Diagnosis/Initial pyruvate carboxylase deficency
Inheritance Familial, autosomal recessive
Diagnosis/Definite pyruvate carboxylase deficency
Age/Examination 02y (2 years)
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Emanuele Coci
Database submission license No license selected
Created by Emanuele Coci
Date created 2019-01-11 14:16:16 +01:00 (CET)
Date last edited 2021-08-11 11:12:14 +02:00 (CEST)

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