Disease #00191 (AMD2A (dysplasia, acromesomelic, type 2A, Grebe), OMIM:200700)
| Official abbreviation |
AMD2A |
| Name |
dysplasia, acromesomelic, type 2A, Grebe |
| OMIM ID |
200700 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal recessive |
| Individuals reported having this disease |
3 |
| Phenotype entries for this disease |
3 |
| Associated with 1 gene |
GDF5 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2013-09-08 14:51:28 +02:00 (CEST) |
| Date last edited |
2021-12-16 17:35:12 +01:00 (CET) |
Individuals
|