Disease #06115 (SSMG;SRMMD (short stature-micrognathia syndrome), OMIM:617164)
| Official abbreviation |
SSMG;SRMMD |
| Name |
short stature-micrognathia syndrome |
| OMIM ID |
617164 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
1 |
| Phenotype entries for this disease |
1 |
| Associated with 1 gene |
ARCN1 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2021-12-10 23:20:41 +01:00 (CET) |
| Date last edited |
2025-02-28 13:05:45 +01:00 (CET) |
Individuals
|