acromesomelic dysplasia, Maroteaux type

Summary
Synonym
  • acromesomelic dysplasia-1
Definition
An acromesomelic dysplasia that has_material_basis_in mutation in NPR-B receptor which results_in severe dwarfism, abnormalities of the vertebral column and shortening of the limb middle and distal segments.
Super Class
acromesomelic dysplasia autosomal recessive disease spinal disease
Disease Ontology
DOID:0080050
Mondo Disease Ontology
MeSH
ORDO
OMIM
GARD
MGI genotype (from TogoID)
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
4882 NPR2 natriuretic peptide receptor 2
Displaying 1 entry
Gene ID Gene Symbol Description Source
230103 Npr2 natriuretic peptide receptor 2
Displaying 1 entry
Gene ID Gene Symbol Description Source
116564 Npr2 natriuretic peptide receptor 2
Displaying 1 entry
Gene ID Gene Symbol Description Source
172051 gcy-28 Receptor-type guanylate cyclase gcy-28

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: December 9, 2024