(Q5883885)
English
holocarboxylase synthetase deficiency
human disease
- Biotin-(propionyl-CoA-carboxylase) ligase deficiency (disorder)
- Multiple carboxylase deficiency - neonatal onset (disorder)
- Multiple carboxylase deficiency - neonatal onset
- Biotin-(propionyl-CoA-carboxylase) ligase deficiency
- Holocarboxylase Synthetase Deficiency
- Multiple Carboxylase Deficiency, Neonatal Form
- Neonatal Multiple Carboxylase Deficiency
- Multiple Carboxylase Deficiency
- Early-onset multiple carboxylase deficiency
- Hlcs Deficiency
- Multiple Carboxylase Deficiency, Early Onset
Statements
2 references
1 reference
4 references
270.8
1 reference
1 reference
Identifiers
Holocarboxylase Synthetase Deficiency
1 reference
1 reference
2 references
2 references
1 reference
1 reference