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PRDM13

PR/SET domain 13

HCNC Approved Symbol
PRDM13 (HGNC:13998)
Genomic Coordinates
6:99,606,833 - 99,615,562 (6q16.2)
Synonyms
PFM10
Disease Associations
This gene is associated with the following 2 diseases in OMIM.
View More Disease Info
Disease NameOMIM IDInheritance
Cerebellar dysfunction, impaired intellectual development, and hypogonadotropic hypogonadism
619761AR
Pontocerebellar hypoplasia, type 17
619909AR

Diagnosed Cases

0Patient

There are no patients diagnosed with a variant in the PRDM13 gene.

Frequently observed phenotypes

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

No Results