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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
carnitine palmitoyltransferase I deficiency
Summary
- Synonym
-
- CPT I deficiency
- CPT1A deficiency
- L-CPT1 deficiency
- carnitine palmitoyl transferase 1A deficiency
- carnitine palmitoyl transferase IA deficiency
- hepatic CPT deficiency type I
- hepatic carnitine palmitoyl transferase 1 deficiency
- hepatic carnitine palmitoyl transferase I deficiency
- Definition
- A lipid metabolism disorder that is characterized by impaired mitochondrial oxidation of long chain fatty acids in the liver and kidneys resulting in episodes of illness- or fasting-induced hypoketotic hypoglycemia, and has_material_basis_in autosomal recessive inheritance of homozygous or compound heterozygous mutation in the carnitine palmitoyltransferase 1A gene (CPT1A) on chromosome 11q13.
- Super Class
- lipid metabolism disorder
External Links
- Disease Ontology
- DOID:0090129
- Mondo Disease Ontology
- ORDO
- OMIM
- GARD
- MGI genotype (from TogoID)
- WikiPathways (from TogoID)
Related Genes
| Gene ID | Gene Symbol | Description | Source |
|---|---|---|---|
| 34 | ACADM | acyl-CoA dehydrogenase medium chain | |
| 1374 | CPT1A | carnitine palmitoyltransferase 1A | |
| 1376 | CPT2 | carnitine palmitoyltransferase 2 | |
| 3295 | HSD17B4 | hydroxysteroid 17-beta dehydrogenase 4 | |
| 5213 | PFKM | phosphofructokinase, muscle | |
| 5224 | PGAM2 | phosphoglycerate mutase 2 |
Related Glycoprotein
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0011463 | Childhood onset |
| HP:0001270 | Motor delay |
| HP:0002014 | Diarrhea |
| HP:0011968 | Feeding difficulties |
| HP:0001324 | Muscle weakness |
| HP:0007335 | Recurrent encephalopathy |
| HP:0001985 | Hypoketotic hypoglycemia |
