Phenotype #0000340278

Individual ID 00451602
Associated disease MCC2D
Phenotype details -
Diagnosis/Initial 3-Methylcrotonyl-CoA carboxylase 2 deficiency
Inheritance Familial, autosomal recessive
Diagnosis/Definite 3-Methylcrotonyl-CoA carboxylase 2 deficiency
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Miriam Erandi Reyna-Fabián
Database submission license Creative Commons Attribution-ShareAlike 4.0 InternationalCreative Commons License
Created by Miriam Erandi Reyna-Fabián
Date created 2024-06-12 22:17:58 +02:00 (CEST)
Date last edited 2024-06-28 09:56:23 +02:00 (CEST)

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