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P4HA2

prolyl 4-hydroxylase subunit alpha 2

HCNC Approved Symbol
P4HA2 (HGNC:8547)
Genomic Coordinates
5:132,190,147 - 132,227,853 (5q31.1)
Synonyms
C-P4Halpha(II), lncRNA-PE
Disease Associations
This gene is associated with the following 1 diseases in OMIM.
View More Disease Info
Disease NameOMIM IDInheritance
Myopia 25, autosomal dominant
617238AD

Diagnosed Cases

0Patient

There are no patients diagnosed with a variant in the P4HA2 gene.

Frequently observed phenotypes

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

No Results