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Repository for lectin-assisted multimodality data
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MIRAGE
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
- GARD
- MGI genotype (from TogoID)
- WikiPathways (from TogoID)
Related Genes
Related Glycoprotein
| UniProt ID | Protein Name | Source |
|---|---|---|
| P07202 | Thyroid peroxidase | |
| Q06710 | Paired box protein Pax-8 | |
| Q92911 | Sodium/iodide cotransporter | |
| Q9NRD8 | Dual oxidase 2 |
| UniProt ID | Protein Name | Source |
|---|---|---|
| O08710 | Thyroglobulin | |
| P21761 | Thyrotropin-releasing hormone receptor | |
| P35419 | Thyroid peroxidase | |
| P47750 | Thyrotropin receptor | |
| Q08775 | Runt-related transcription factor 2 |
| UniProt ID | Protein Name | Source |
|---|---|---|
| P12839 | Neurofilament medium polypeptide | |
| P16884 | Neurofilament heavy polypeptide | |
| P19527 | Neurofilament light polypeptide | |
| P21463 | Thyrotropin receptor |
