Disease #05621 (MKHK1 (Menke-Hennekam syndrome, type 1 (MKHK-1)), OMIM:618332)
Official abbreviation |
MKHK1 |
Name |
Menke-Hennekam syndrome, type 1 (MKHK-1) |
OMIM ID |
618332 |
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 |
CREBBP |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2019-07-05 14:50:59 +02:00 (CEST) |
Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
|