Disease #05770 (KLEFS2 (Kleefstra syndrome, type 2 (KLEFS2)), OMIM:617768)
| Official abbreviation |
KLEFS2 |
| Name |
Kleefstra syndrome, type 2 (KLEFS2) |
| OMIM ID |
617768 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
5 |
| Phenotype entries for this disease |
4 |
| Associated with 1 gene |
MLL3 |
| Associated tissues |
- |
| Disease features |
developmental delay, intellectual disability, behavioral and psychiatric problems, hypotonia, seizures, short stature |
| Remarks |
- |
| Date created |
2020-06-12 11:39:49 +02:00 (CEST) |
| Date last edited |
2024-08-15 19:32:11 +02:00 (CEST) |
Individuals
|
Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.
|