Disease #07221 (MRD75 (intellectual developmental disorder, autosomal dominant, type 75), OMIM:620988)
| Official abbreviation |
MRD75 |
| Name |
intellectual developmental disorder, autosomal dominant, type 75 |
| OMIM ID |
620988 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
DHX9 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2025-12-18 16:03:37 +01:00 (CET) |
| Date last edited |
N/A |
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