Disease #00596 (TD1 (dysplasia, thanatophoric, type I (TD1)), OMIM:187600)
| Official abbreviation |
TD1 |
| Name |
dysplasia, thanatophoric, type I (TD1) |
| OMIM ID |
187600 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
FGFR3 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
2021-10-22 16:19:52 +02:00 (CEST) |
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