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PKHD1L1

PKHD1 like 1

HCNC Approved Symbol
PKHD1L1 (HGNC:20313)
Genomic Coordinates
8:109,362,461 - 109,537,207 (8q23.1-q23.2)
Synonyms
Disease Associations
This gene is associated with the following 1 diseases in OMIM.
View More Disease Info
Disease NameOMIM IDInheritance
Deafness, autosomal recessive 124
620794AR

Diagnosed Cases

0Patient

There are no patients diagnosed with a variant in the PKHD1L1 gene.

Frequently observed phenotypes

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

No Results