Weissenbacher-Zweymuller syndrome

Summary
Synonym
  • Piere-Robin syndrome
  • Pierre Robin Malformation
Definition
An osteochondrodysplasia that results_in shortened long bones and distinct facial abnormalities.
Super Class
osteochondrodysplasia
External Links
Disease Ontology
DOID:4258
Mondo Disease Ontology
MeSH
UMLS
NCI Thesaurus
OMIM
MGI genotype (from TogoID)
Related Genes
Displaying entry 21 - 21 of 21 in total
Gene ID Gene Symbol Description Source
158326 FREM1 FRAS1 related extracellular matrix 1

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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: August 19, 2024