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
Disease Ontology
DOID:4258
Mondo Disease Ontology
MeSH
UMLS
NCI Thesaurus
OMIM
MGI genotype (from TogoID)
Related Genes
Displaying all 2 entries
Gene ID Gene Symbol Description Source
92 ACVR2A activin A receptor type 2A
7037 TFRC transferrin receptor
Displaying all 2 entries
Gene ID Gene Symbol Description Source
11480 Acvr2a activin receptor IIA
22042 Tfrc transferrin receptor
Displaying all 2 entries
Gene ID Gene Symbol Description Source
29263 Acvr2a activin A receptor type 2A
64678 Tfrc transferrin receptor
Displaying 1 entry
Gene ID Gene Symbol Description Source
175781 daf-4 Cell surface receptor daf-4;Serine/threonine-protein kinase receptor;receptor protein serine/threonine kinase
Displaying all 2 entries
Gene ID Gene Symbol Description Source
854430 TRE2 putative zinc metalloprotease
855927 TRE1 Tre1p

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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