Primary Hypertrophic Osteoarthropathy (PDP)

Alias:
Pachydermoperiostosis
Osteoarthropathy, Primary Hypertrophic
Touraine-Solente-Gole Syndrome
Pdp
Idiopathic Hypertrophic Osteoarthropathy
Pachydermoperiostosis Syndrome
Pachydermoperiostosis of Nail
Pho
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Primary Hypertrophic Osteoarthropathy, also known as pachydermoperiostosis, is related to hypertrophic osteoarthropathy, primary, autosomal recessive, 1 and secondary hypertrophic osteoarthropathy, and has symptoms including arthralgia, flushing and metatarsalgia. An important gene associated with Primary Hypertrophic Osteoarthropathy is HPGD (15-Hydroxyprostaglandin Dehydrogenase), and among its related pathways/superpathways are Fatty acid metabolism and Beta-2 adrenergic-dependent CFTR expression. The drugs Etoricoxib and Narcotics have been mentioned in the context of this disorder. Affiliated tissues include bone and skin, and related phenotypes are hyperhidrosis and abnormal cortical bone morphology
Related ID:
MESH:D010004

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AR
Newborn
--
14
85
--

Medical Symptom

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Categorization
Description
HPO Frequency
Orphanet Frequency
HPO Source Accession
No data available

Gene & Mutation

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Gene
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Score
Mutations
No data available

Related Drugs

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CAS Number
Status
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No data available

Disease Model

Category
Name
MGI
Related Gene
Strain of Origin
Publications
No data available

References Literature

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PMID
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IF
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