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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 |
|---|---|---|---|
| 2876 | GPX1 | glutathione peroxidase 1 | |
| 3283 | HSD3B1 | hydroxy-delta-5-steroid dehydrogenase, 3 beta- and steroid delta-isomerase 1 | |
| 3293 | HSD17B3 | hydroxysteroid 17-beta dehydrogenase 3 | |
| 3633 | INPP5B | inositol polyphosphate-5-phosphatase B | |
| 3897 | L1CAM | L1 cell adhesion molecule | |
| 3958 | LGALS3 | galectin 3 | |
| 3990 | LIPC | lipase C, hepatic type | |
| 4153 | MBL2 | mannose binding lectin 2 | |
| 4684 | NCAM1 | neural cell adhesion molecule 1 | |
| 5167 | ENPP1 | ectonucleotide pyrophosphatase/phosphodiesterase 1 |
Related Glycoprotein
