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HPGD

15-hydroxyprostaglandin dehydrogenase

HCNC Approved Symbol
HPGD (HGNC:5154)
Genomic Coordinates
4:174,490,175 - 174,522,893 (4q34.1)
Synonyms
SDR36C1
Disease Associations
This gene is associated with the following 3 diseases in OMIM.
View More Disease Info
Disease NameOMIM IDInheritance
?Digital clubbing, isolated congenital
119900AR
Cranioosteoarthropathy
259100AR
Hypertrophic osteoarthropathy, primary, autosomal recessive 1
259100AR

Diagnosed Cases

1Patient

In total, 1 patient was diagnosed with a variant in the HPGD gene.

Frequently observed phenotypes

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

Abnormal nails
 1 (100.0%)
Abnormality of the nail
 1 (100.0%)
Ichthyosis
 1 (100.0%)
Onychogryposis
 1 (100.0%)
Thick nail
 1 (100.0%)