Disease #06941 (MRD67 (intellectual developmental disorder, autosomal dominant, type 67), OMIM:619927)
| Official abbreviation |
MRD67 |
| Name |
intellectual developmental disorder, autosomal dominant, type 67 |
| OMIM ID |
619927 |
| 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 |
GRIA1 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2022-06-30 19:41:11 +02:00 (CEST) |
| Date last edited |
N/A |
Individuals
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