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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 |
|---|---|---|---|
| 19017 | Ppargc1a | peroxisome proliferative activated receptor, gamma, coactivator 1 alpha | |
| 21819 | Tg | thyroglobulin | |
| 22018 | Tpo | thyroid peroxidase | |
| 22045 | Trhr | thyrotropin releasing hormone receptor | |
| 22095 | Tshr | thyroid stimulating hormone receptor | |
| 99439 | Duox1 | dual oxidase 1 | |
| 380684 | Nefh | neurofilament, heavy polypeptide |
| Gene ID | Gene Symbol | Description | Source |
|---|---|---|---|
| 24377 | G6pd | glucose-6-phosphate dehydrogenase | |
| 24588 | Nefm | neurofilament medium chain | |
| 24596 | Ngfr | nerve growth factor receptor | |
| 25196 | Inhbb | inhibin subunit beta B | |
| 25235 | Ghr | growth hormone receptor | |
| 25360 | Tshr | thyroid stimulating hormone receptor | |
| 25570 | Trhr | thyrotropin releasing hormone receptor | |
| 79107 | Duox2 | dual oxidase 2 | |
| 83516 | Ppargc1a | PPARG coactivator 1 alpha | |
| 83613 | Nefl | neurofilament light chain |
