Disease #00792 (MRD1 (mental retardation, autosomal dominant, type 1 (MRD-1)), OMIM:156200)
Official abbreviation |
MRD1 |
Name |
mental retardation, autosomal dominant, type 1 (MRD-1) |
OMIM ID |
156200 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal dominant |
Individuals reported having this disease |
2 |
Phenotype entries for this disease |
2 |
Associated with 1 gene |
MBD5 |
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
|