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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
congenital hypothyroidism
Summary
- Definition
- A hypothyroidism that is present at birth.
- Super Class
- hypothyroidism physical disorder
External Links
- Disease Ontology
- DOID:0050328
- Mondo Disease Ontology
- MeSH
- UMLS
- NCI Thesaurus
- OMIM
- GARD
- MGI genotype (from TogoID)
- WikiPathways (from TogoID)
Related Genes
| Gene ID | Gene Symbol | Description | Source |
|---|---|---|---|
| 29988 | SLC2A8 | solute carrier family 2 member 8 | |
| 79053 | ALG8 | ALG8 alpha-1,3-glucosyltransferase | |
| 79644 | SRD5A3 | steroid 5 alpha-reductase 3 | |
| 80339 | PNPLA3 | patatin like phospholipase domain containing 3 | |
| 126129 | CPT1C | carnitine palmitoyltransferase 1C | |
| 145173 | B3GLCT | beta 3-glucosyltransferase | |
| 148738 | HJV | hemojuvelin BMP co-receptor | |
| 154091 | SLC2A12 | solute carrier family 2 member 12 |
Related Glycoprotein
| UniProt ID | Protein Name | Source |
|---|---|---|
| Q6ZVN8 | Hemojuvelin | |
| Q8TD20 | Solute carrier family 2, facilitated glucose transporter member 12 | |
| Q93063 | Exostosin-2 | |
| Q9NST1 | 1-acylglycerol-3-phosphate O-acyltransferase PNPLA3 | |
| Q9NY64 | Solute carrier family 2, facilitated glucose transporter member 8 |
