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MEOX1

mesenchyme homeobox 1

HCNC Approved Symbol
MEOX1 (HGNC:7013)
Genomic Coordinates
17:43,640,389 - 43,661,922 (17q21.31)
Synonyms
MOX1
Disease Associations
This gene is associated with the following 1 diseases in OMIM.
View More Disease Info
Disease NameOMIM IDInheritance
Klippel-Feil syndrome 2
214300AR

Diagnosed Cases

0Patient

There are no patients diagnosed with a variant in the MEOX1 gene.

Frequently observed phenotypes

(Top 5 only, Patient count*)
*% of total patients presenting each phenotype is shown in parentheses.

No Results