Disease #00019 (MRX-17;MRX-31 (mental retardation, X-linked, type 17/31 (MRX-17;MRX-31, chromosome Xp11.22 duplication syndrome)), OMIM:300705)
| Official abbreviation |
MRX-17;MRX-31 |
| Name |
mental retardation, X-linked, type 17/31 (MRX-17;MRX-31, chromosome Xp11.22 duplication syndrome) |
| OMIM ID |
300705 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
- |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
HSD17B10 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2012-07-23 10:51:23 +02:00 (CEST) |
| Date last edited |
N/A |
|
