TARP syndrome

Summary
Synonym
  • Pierre Robin sequence-congenital heart defect-talipes syndrome
  • Pierre Robin syndrome-congenital heart defect-talipes syndrome
  • TARPS
  • talipes equinovarus-atrial septal defect-Robin sequence-persistence of the left superior vena cava syndrome
Definition
A syndrome characterized by talipes equinovarus, atrial septal defect, Robin sequence (micrognathia, cleft palate, and glossoptosis), and persistent left superior vena cava typically resulting in late prenatal or early postnatal mortality that has_material_basis_in hemizygous mutation in the RBM10 gene on chromosome Xp11.3.
Super Class
X-linked monogenic disease syndrome
Disease Ontology
DOID:0111780
Mondo Disease Ontology
MeSH
UMLS
ORDO
OMIM
GARD
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
8241 RBM10 RNA binding motif protein 10
Displaying 1 entry
Gene ID Gene Symbol Description Source
236732 Rbm10 RNA binding motif protein 10

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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