Disease #04076 (MRD23 (mental retardation, autosomal dominant, type 23 (MRD-23)), OMIM:615761)
| Official abbreviation |
MRD23 |
| Name |
mental retardation, autosomal dominant, type 23 (MRD-23) |
| OMIM ID |
615761 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
4 |
| Phenotype entries for this disease |
4 |
| Associated with 1 gene |
SETD5 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
|