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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 |
|---|---|---|---|
| 43 | ACHE | acetylcholinesterase (Yt blood group) | |
| 308 | ANXA5 | annexin A5 | |
| 410 | ARSA | arylsulfatase A | |
| 427 | ASAH1 | N-acylsphingosine amidohydrolase 1 | |
| 570 | BAAT | bile acid-CoA:amino acid N-acyltransferase | |
| 847 | CAT | catalase | |
| 1012 | CDH13 | cadherin 13 | |
| 1312 | COMT | catechol-O-methyltransferase | |
| 1555 | CYP2B6 | cytochrome P450 family 2 subfamily B member 6 | |
| 1588 | CYP19A1 | cytochrome P450 family 19 subfamily A member 1 |
Related Glycoprotein
| UniProt ID | Protein Name | Source |
|---|---|---|
| Q6ZVN8 | Hemojuvelin | |
| Q8TD20 | Solute carrier family 2, facilitated glucose transporter member 12 | |
| Q93063 | Exostosin-2 | |
| Q9NST1 | 1-acylglycerol-3-phosphate O-acyltransferase PNPLA3 | |
| Q9NY64 | Solute carrier family 2, facilitated glucose transporter member 8 |
