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DLX5

distal-less homeobox 5

HCNC Approved Symbol
DLX5 (HGNC:2918)
Genomic Coordinates
7:97,020,396 - 97,024,831 (7q21.3)
Synonyms
Disease Associations
This gene is associated with the following 2 diseases in OMIM.
View More Disease Info
Disease NameOMIM IDInheritance
?Split-hand/foot malformation 1 with sensorineural hearing loss
220600AR
Split-hand/foot malformation 1
183600AD

Diagnosed Cases

0Patient

There are no patients diagnosed with a variant in the DLX5 gene.

Frequently observed phenotypes

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

No Results