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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 |
|---|---|---|
| P15104 | Glutamine synthetase | |
| P15289 | Arylsulfatase A | |
| P17931 | Galectin-3 | |
| P21964 | Catechol O-methyltransferase | |
| P22303 | Acetylcholinesterase | |
| P22413 | Ectonucleotide pyrophosphatase/phosphodiesterase family member 1 | |
| P32004 | Neural cell adhesion molecule L1 | |
| P32019 | Type II inositol 1,4,5-trisphosphate 5-phosphatase | |
| P35052 | Glypican-1 | |
| P35354 | Prostaglandin G/H synthase 2 |
