Disease #05621 (MKHK-1 (syndrome, Menke-Hennekam, type 1 (MKHK-1)), OMIM:618332)

Official abbreviation MKHK-1
Name syndrome, Menke-Hennekam, type 1 (MKHK-1)
OMIM ID 618332
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene CREBBP
Associated tissues -
Disease features -
Remarks -