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FGF20

fibroblast growth factor 20

HCNC Approved Symbol
FGF20 (HGNC:3677)
Genomic Coordinates
8:16,992,181 - 17,002,345 (8p22)
Synonyms
Disease Associations
This gene is associated with the following 1 diseases in OMIM.
View More Disease Info
Disease NameOMIM IDInheritance
?Renal hypodysplasia/aplasia 2
615721AR

Diagnosed Cases

0Patient

There are no patients diagnosed with a variant in the FGF20 gene.

Frequently observed phenotypes

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

No Results