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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 |
|---|---|---|---|
| 1636 | ACE | angiotensin I converting enzyme | |
| 1946 | EFNA5 | ephrin A5 | |
| 2026 | ENO2 | enolase 2 | |
| 2132 | EXT2 | exostosin glycosyltransferase 2 | |
| 2194 | FASN | fatty acid synthase | |
| 2517 | FUCA1 | alpha-L-fucosidase 1 | |
| 2539 | G6PD | glucose-6-phosphate dehydrogenase | |
| 2619 | GAS1 | growth arrest specific 1 | |
| 2752 | GLUL | glutamate-ammonia ligase | |
| 2817 | GPC1 | glypican 1 |
Related Glycoprotein
