Disease #06848 (MRXS33 (Mental retardation, X-linked, syndromic 33), OMIM:300966)
| Official abbreviation |
MRXS33 |
| Name |
Mental retardation, X-linked, syndromic 33 |
| OMIM ID |
300966 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
X-linked recessive |
| Individuals reported having this disease |
1 |
| Phenotype entries for this disease |
1 |
| Associated with 1 gene |
TAF1 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2021-12-10 23:20:41 +01:00 (CET) |
| Date last edited |
N/A |
Individuals
|