Disease #02267 (STHAGX1 (agenesis, tooth, selective, X-linked, type 1 (STHAGX1)), OMIM:313500)
| Official abbreviation |
STHAGX1 |
| Name |
agenesis, tooth, selective, X-linked, type 1 (STHAGX1) |
| OMIM ID |
313500 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
X-linked dominant |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
EDA |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
2020-05-18 09:47:01 +02:00 (CEST) |
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