Pseudoachondroplasia (PSACH)

Alias:
Pseudoachondroplastic Dysplasia
Psach
Pseudoachondroplastic Spondyloepiphyseal Dysplasia Syndrome
Spondyloepiphyseal Dysplasia, Pseudoachondroplastic
Pseudoachondroplastic Spondyloepiphyseal Dysplasia
Spondyloepiphyseal Dysplasia Pseudoachondroplastic
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Pseudoachondroplasia, also known as pseudoachondroplastic dysplasia, is related to epiphyseal dysplasia, multiple, 1 and cartilage disease, and has symptoms including ulnar deviation of the wrist and waddling gait. An important gene associated with Pseudoachondroplasia is COMP (Cartilage Oligomeric Matrix Protein), and among its related pathways/superpathways are Integrin Pathway and Phospholipase-C Pathway. The drugs Resveratrol and Platelet Aggregation Inhibitors have been mentioned in the context of this disorder. Affiliated tissues include bone and bone marrow, and related phenotypes are joint laxity and disproportionate short-limb short stature
Related ID:
MESH:C535819
ICD11:1192649257

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AD
Newborn
--
18
121
76

Medical Symptom

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Gene & Mutation

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Disease Model

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MGI
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Publications
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References Literature

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