3billion
back to listBack to List

WNT7A

Wnt family member 7A

HCNC Approved Symbol
WNT7A (HGNC:12786)
Genomic Coordinates
3:13,816,258 - 13,880,071 (3p25.1)
Synonyms
Wnt-7a
Disease Associations
This gene is associated with the following 2 diseases in OMIM.
View More Disease Info
Disease NameOMIM IDInheritance
Fuhrmann syndrome
228930AR
Ulna and fibula, absence of, with severe limb deficiency
276820AR

Diagnosed Cases

0Patient

There are no patients diagnosed with a variant in the WNT7A gene.

Frequently observed phenotypes

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

No Results