Disease #00376 (SRTD5 (dysplasia, short-rib thoracic, type 5, with/without polydactyly (SRTD-5)), OMIM:614376)
| Official abbreviation |
SRTD5 |
| Name |
dysplasia, short-rib thoracic, type 5, with/without polydactyly (SRTD-5) |
| OMIM ID |
614376 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal recessive |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
WDR19 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-05-02 09:59:17 +02:00 (CEST) |
| Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
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