Phenotype #0000307855

Individual ID 00416089
Associated disease COQ10D
Phenotype details see paper; ... (esp. treatment), 3d-died cardio-respiratory failure; normal intrauterine growth; birth full term; delayed motor development; delayed cognitive development; developmental stagnation/minimal development; 1d-seizures; 3d-respiratory distress/insufficiency; cardiomegaly;
Diagnosis/Initial neurodevelopmental delay
Inheritance Familial, autosomal recessive
Diagnosis/Definite -
Age/Examination 2d
Age/Diagnosis -
Age/Onset 1d
Phenotype/Onset respiratory distress
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 2022-08-22 19:29:13 +02:00 (CEST)
Date last edited N/A

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