Disease #00379 (SRTD1 (dysplasia, short-rib thoracic, type 1, with/without polydactyly (SRTD-1, dystrophy, asphyxiating thoracic; Jeune syndrome)), OMIM:208500)
| Official abbreviation |
SRTD1 |
| Name |
dysplasia, short-rib thoracic, type 1, with/without polydactyly (SRTD-1, dystrophy, asphyxiating thoracic; Jeune syndrome) |
| OMIM ID |
208500 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
- |
| Individuals reported having this disease |
9 |
| Phenotype entries for this disease |
4 |
| Associated with 0 genes |
- |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-05-02 10:26:00 +02:00 (CEST) |
| Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
|