Disease #00822 (MRX1 (mental retardation, X-linked, type 1), OMIM:309530)
| Official abbreviation |
MRX1 |
| Name |
mental retardation, X-linked, type 1 |
| OMIM ID |
309530 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
X-linked dominant |
| Individuals reported having this disease |
4 |
| Phenotype entries for this disease |
2 |
| Associated with 1 gene |
IQSEC2 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
2022-11-25 16:08:47 +01:00 (CET) |
Individuals
|