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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 |
|---|---|---|---|
| 5743 | PTGS2 | prostaglandin-endoperoxide synthase 2 | |
| 6515 | SLC2A3 | solute carrier family 2 member 3 | |
| 6715 | SRD5A1 | steroid 5 alpha-reductase 1 | |
| 8879 | SGPL1 | sphingosine-1-phosphate lyase 1 | |
| 8985 | PLOD3 | procollagen-lysine,2-oxoglutarate 5-dioxygenase 3 | |
| 9415 | FADS2 | fatty acid desaturase 2 | |
| 9526 | MPDU1 | mannose-P-dolichol utilization defect 1 | |
| 10020 | GNE | glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase | |
| 10891 | PPARGC1A | PPARG coactivator 1 alpha | |
| 23583 | SMUG1 | single-strand-selective monofunctional uracil-DNA glycosylase 1 |
Related Glycoprotein
