Medicine and Dentistry
Leukocyte
100%
Autosomal Recessive Inheritance
100%
2 Oxoglutaric Acid
100%
Oxoglutarate Dehydrogenase
100%
Fibroblast
100%
Urinary System
50%
Clinical Feature
50%
Carboxylyase
50%
Sensorineural Hearing Loss
50%
Biochemical Marker
50%
Thumb
50%
Osteodystrophy
50%
Diseases
50%
Keyphrases
2-Oxoglutarate Dehydrogenase Complex
100%
DOOR Syndrome
100%
2-oxoglutarate
66%
White Blood Cells
66%
Autosomal Recessive
66%
Fibroblasts
33%
Clinical Features
33%
Thumb
33%
Urinary Levels
33%
Dystrophic
33%
Biochemical Markers
33%
Patient Fibroblasts
33%
Decarboxylase
33%
Sensorineural Deafness
33%
Osteodystrophy
33%
Biochemistry, Genetics and Molecular Biology
Leukocyte
100%
Autosomal Recessive Inheritance
100%
Oxoglutarate Dehydrogenase Complex
100%
Fibroblast
100%
Deficiency
100%
Carboxy-Lyases
50%
Urine Level
50%