Phenotype #0000258075

Individual ID 00362705
Associated disease MLYCDD
Phenotype details see paper; ..., developmental delay, acidosis, hypoglycaemia
Diagnosis/Initial -
Inheritance Familial, autosomal recessive
Diagnosis/Definite -
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2021-04-22 19:44:39 +02:00 (CEST)
Date last edited 2021-04-23 15:19:09 +02:00 (CEST)

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