Disease #00185 (ACGA (chondrodysplasia, acromesomelic, with genital anomalies (ACGA)), OMIM:609441)
| Official abbreviation |
ACGA |
| Name |
chondrodysplasia, acromesomelic, with genital anomalies (ACGA) |
| OMIM ID |
609441 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
- |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
BMPR1B |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2013-09-02 22:20:13 +02:00 (CEST) |
| Date last edited |
N/A |
|
|