Disease #00121 (TPBS (brachydactyly, Temtamy, preaxial, syndrome (TPBS)), OMIM:605282)
| Official abbreviation |
TPBS |
| Name |
brachydactyly, Temtamy, preaxial, syndrome (TPBS) |
| OMIM ID |
605282 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal recessive |
| Individuals reported having this disease |
1 |
| Phenotype entries for this disease |
1 |
| Associated with 1 gene |
CHSY1 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2013-04-18 09:31:07 +02:00 (CEST) |
| Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
|