Disease #00380 (SRTD-3;SRPS-2B (dysplasia, thoracic, short-rib, type 3 with or without polydactyly (SRTD-3, short rib polydactyly syndrome 2B (SRPS-2B))), OMIM:613091)
| Official abbreviation |
SRTD-3;SRPS-2B |
| Name |
dysplasia, thoracic, short-rib, type 3 with or without polydactyly (SRTD-3, short rib polydactyly syndrome 2B (SRPS-2B)) |
| OMIM ID |
613091 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
- |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
DYNC2H1 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-05-02 17:15:21 +02:00 (CEST) |
| Date last edited |
N/A |
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