Disease #04619 (WHSUS;MRD37 (White-Sutton syndrome (WHSUS, mental retardation, autosomal dominant, type 37 (MRD-37))), OMIM:616364)
| Official abbreviation |
WHSUS;MRD37 |
| Name |
White-Sutton syndrome (WHSUS, mental retardation, autosomal dominant, type 37 (MRD-37)) |
| OMIM ID |
616364 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
3 |
| Phenotype entries for this disease |
3 |
| Associated with 1 gene |
POGZ |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2015-09-23 10:25:23 +02:00 (CEST) |
| Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
|