Hypertrophic Osteoarthropathy(Pachydermoperiostosis) Explore Disorder's Alias
An Autosomal recessive mode(s) within the Bone disorders category
Candidate Gene Information
An Autosomal recessive mode(s) within the Bone disorders category
Reported Pathogenic variants
| S.No. | Name/GeneID | Description | Cytogentic Band | Gene Location on genomic DNA | Gene Length | Exons | Details | Gene Cross-References |
| 1 | HPGD/3248 | 15-hydroxyprostaglandin dehydrogenase | 4q34.1 | Chr4, NC_000004.12 (174490175..174522893, complement) |
32719 nt | 10 | More... | OMIM gene gnomAD browser EnsEMBL GeneCards ClinGen gene |
| 2 | SLCO2A1/6578 | solute carrier organic anion transporter family member 2A1 | 3q22.1 | Chr3, NC_000003.12 (133932701..134029925, complement) |
97225 nt | 14 | More... | OMIM gene gnomAD browser EnsEMBL GeneCards ClinGen gene |
| Variant Information | ||||||||
| Disorder Cross-References: GARD GTR MalaCards NORD | ||||||||
Patient care services
Clinical Symptoms & Disabilities
Prevalence
| Under development |