Disease #04354 (FDAH (hyperthyroxinemia, dysalbuminemic (FDAH)), OMIM:615999)
| Official abbreviation |
FDAH |
| Name |
hyperthyroxinemia, dysalbuminemic (FDAH) |
| OMIM ID |
615999 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
- |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
ALB |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2015-09-23 10:25:22 +02:00 (CEST) |
| Date last edited |
2015-12-08 23:53:05 +01:00 (CET) |
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