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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