Disease #02096 (TDH1 (thyroid dyshormonogenesis, type 1 (TDH1)), OMIM:274400)
| Official abbreviation |
TDH1 |
| Name |
thyroid dyshormonogenesis, type 1 (TDH1) |
| OMIM ID |
274400 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal recessive |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
SLC5A5 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
2020-09-14 09:37:54 +02:00 (CEST) |
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