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EPS8

EGFR pathway substrate 8, signaling adaptor

HCNC Approved Symbol
EPS8 (HGNC:3420)
Genomic Coordinates
12:15,620,134 - 15,789,388 (12p12.3)
Synonyms
Disease Associations
This gene is associated with the following 1 diseases in OMIM.
View More Disease Info
Disease NameOMIM IDInheritance
?Deafness, autosomal recessive 102
615974AR

Diagnosed Cases

0Patient

There are no patients diagnosed with a variant in the EPS8 gene.

Frequently observed phenotypes

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

No Results