Disease #06007 (MRD42 (Mental retardation, autosomal dominant 42), OMIM:616973)
Official abbreviation |
MRD42 |
Name |
Mental retardation, autosomal dominant 42 |
OMIM ID |
616973 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal dominant |
Individuals reported having this disease |
2 |
Phenotype entries for this disease |
2 |
Associated with 1 gene |
GNB1 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2021-12-10 23:20:41 +01:00 (CET) |
Date last edited |
N/A |
Individuals
|
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