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
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