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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
umbilical hernia
Summary
- Definition
- A intestinal disease characterized by the protrusion by part of the intestine though an opening in the abdominal muscles.
- Super Class
- intestinal disease
External Links
- Disease Ontology
- DOID:0060321
- Mondo Disease Ontology
- MeSH
- UMLS
- NCI Thesaurus
Related Genes
| Gene ID | Gene Symbol | Description | Source |
|---|---|---|---|
| 175 | AGA | aspartylglucosaminidase | |
| 411 | ARSB | arylsulfatase B | |
| 1312 | COMT | catechol-O-methyltransferase | |
| 1836 | SLC26A2 | solute carrier family 26 member 2 | |
| 2719 | GPC3 | glypican 3 | |
| 2990 | GUSB | glucuronidase beta | |
| 3423 | IDS | iduronate 2-sulfatase | |
| 3955 | LFNG | LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase | |
| 4952 | OCRL | OCRL inositol polyphosphate-5-phosphatase | |
| 5048 | PAFAH1B1 | platelet activating factor acetylhydrolase 1b regulatory subunit 1 |
Related Glycoprotein
| UniProt ID | Protein Name | Source |
|---|---|---|
| Q9NR19 | Acetyl-coenzyme A synthetase, cytoplasmic | |
| Q9Y487 | V-type proton ATPase 116 kDa subunit a 2 | |
| Q9Y625 | Glypican-6 | |
| Q9Y6Z7 | Collectin-10 |
