Disease #05769 (KLEFS1 (Kleefstra syndrome, type 1 (KLEFS1)), OMIM:610253)
Official abbreviation |
KLEFS1 |
Name |
Kleefstra syndrome, type 1 (KLEFS1) |
OMIM ID |
610253 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal dominant |
Individuals reported having this disease |
12 |
Phenotype entries for this disease |
5 |
Associated with 1 gene |
EHMT1 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2020-06-12 11:38:53 +02:00 (CEST) |
Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
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