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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
congenital generalized lipodystrophy type 3
Summary
- Synonym
-
- Berardinelli-Seip congenital lipodystrophy type 3
- Definition
- A congenital generalized lipodystrophy that has_material_basis_in an autosomal recessive mutation of CAV1 on chromosome 7q31.2.
- Super Class
- congenital generalized lipodystrophy
External Links
- Disease Ontology
- DOID:0111137
- Mondo Disease Ontology
- OMIM
- WikiPathways (from TogoID)
Related Genes
| Gene ID | Gene Symbol | Description | Source |
|---|---|---|---|
| 178 | AGL | amylo-alpha-1, 6-glucosidase, 4-alpha-glucanotransferase | |
| 523 | ATP6V1A | ATPase H+ transporting V1 subunit A | |
| 952 | CD38 | CD38 molecule | |
| 1650 | DDOST | dolichyl-diphosphooligosaccharide--protein glycosyltransferase non-catalytic subunit | |
| 2218 | FKTN | fukutin | |
| 2517 | FUCA1 | alpha-L-fucosidase 1 | |
| 2719 | GPC3 | glypican 3 | |
| 4023 | LPL | lipoprotein lipase | |
| 5105 | PCK1 | phosphoenolpyruvate carboxykinase 1 | |
| 5130 | PCYT1A | phosphate cytidylyltransferase 1A, choline |
Related Glycoprotein
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0001833 | Long foot |
| HP:0000336 | Prominent supraorbital ridges |
| HP:0005616 | Accelerated skeletal maturation |
| HP:0001176 | Large hands |
| HP:0010465 | Precocious puberty in females |
| HP:0001397 | Hepatic steatosis |
| HP:0000876 | Oligomenorrhea |
| HP:0002240 | Hepatomegaly |
| HP:0000141 | Amenorrhea |
| HP:0001639 | Hypertrophic cardiomyopathy |
