Disease #00831 (MRX97 (mental retardation, X-linked, type 97 (MRX97)), OMIM:300803)
| Official abbreviation |
MRX97 |
| Name |
mental retardation, X-linked, type 97 (MRX97) |
| OMIM ID |
300803 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
X-linked |
| Individuals reported having this disease |
2 |
| Phenotype entries for this disease |
1 |
| Associated with 1 gene |
ZNF711 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
2020-05-11 17:00:09 +02:00 (CEST) |
Individuals
|