Disease #00124 (MFDGA;MFDM (dysostosis, mandibulofacial, Guion-Almeida type (MFDGA, mandibulofacial dysostosis with microcephaly (MFDM))), OMIM:610536)
| Official abbreviation |
MFDGA;MFDM |
| Name |
dysostosis, mandibulofacial, Guion-Almeida type (MFDGA, mandibulofacial dysostosis with microcephaly (MFDM)) |
| OMIM ID |
610536 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
- |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
EFTUD2 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2013-05-02 11:49:16 +02:00 (CEST) |
| Date last edited |
N/A |
|
