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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
progeria
Summary
- Synonym
-
- HGPS
- Hutchinson Gilford syndrome
- Hutchinson-Gilford Progeria syndrome
- Hutchinson-Gilford disease
- Definition
- A progeroid syndrome characterized by extreme short stature, low body weight, early loss of hair, lipodystrophy, scleroderma, decreased joint mobility, osteolysis, and facial features that resemble aged persons that has_material_basis_in mutation in the LMNA gene on chromosome 1q22.
- Super Class
- autosomal dominant disease progeroid syndrome
External Links
- Disease Ontology
- DOID:3911
- Mondo Disease Ontology
- MeSH
- UMLS
- NCI Thesaurus
- ORDO
- OMIM
- GARD
- MGI genotype (from TogoID)
- WikiPathways (from TogoID)
Related Genes
| Gene ID | Gene Symbol | Description | Source |
|---|---|---|---|
| 2224 | FDPS | farnesyl diphosphate synthase | |
| 2539 | G6PD | glucose-6-phosphate dehydrogenase | |
| 2645 | GCK | glucokinase | |
| 2678 | GGT1 | gamma-glutamyltransferase 1 | |
| 2739 | GLO1 | glyoxalase I | |
| 2990 | GUSB | glucuronidase beta | |
| 3383 | ICAM1 | intercellular adhesion molecule 1 | |
| 4968 | OGG1 | 8-oxoguanine DNA glycosylase | |
| 5563 | PRKAA2 | protein kinase AMP-activated catalytic subunit alpha 2 | |
| 5631 | PRPS1 | phosphoribosyl pyrophosphate synthetase 1 |
