Disease #05902 (MRD55 (mental retardation, autosomal dominant, type 55, with seizures), OMIM:617831)
Official abbreviation |
MRD55 |
Name |
mental retardation, autosomal dominant, type 55, with seizures |
OMIM ID |
617831 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal dominant |
Individuals reported having this disease |
1 |
Phenotype entries for this disease |
1 |
Associated with 1 gene |
NUS1 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2021-03-03 09:31:02 +01:00 (CET) |
Date last edited |
2023-10-23 15:21:12 +02:00 (CEST) |
Individuals
|