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MIRAGE
split hand-foot malformation 6

Summary
Synonym
  • SHFM6
Definition
A split-hand/foot malformation that has_material_basis_in homozygous mutation in the WNT10B gene on chromosome 12q13.
Super Class
autosomal recessive disease split hand-foot malformation
Disease Ontology
DOID:0090026
MeSH
UMLS
NCI Thesaurus
ORDO
WikiPathways (from TogoID)
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
7480 WNT10B Wnt family member 10B
Related Glycoprotein
Displaying 1 entry
UniProt ID Protein Name Source
O00744 Protein Wnt-10b
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GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

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

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Last updated: December 8, 2025