Disease #07155 (MRD64 (intellectual developmental disorder, autosomal dominant, type 64), OMIM:619188)
Official abbreviation |
MRD64 |
Name |
intellectual developmental disorder, autosomal dominant, type 64 |
OMIM ID |
619188 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal dominant |
Individuals reported having this disease |
- |
Phenotype entries for this disease |
- |
Associated with 1 gene |
ZNF292 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2025-03-06 14:07:33 +01:00 (CET) |
Date last edited |
N/A |
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