Disease #00842 (GAND;MRD18 (GAND syndrome (GAND, MRD18)), OMIM:615074)
Official abbreviation |
GAND;MRD18 |
Name |
GAND syndrome (GAND, MRD18) |
OMIM ID |
615074 |
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 |
GATAD2B |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
|