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Standards Ontologies Notations
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
Mondo Disease Ontology
MeSH
UMLS
NCI Thesaurus
ORDO
OMIM
WikiPathways (from TogoID)
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
7480 WNT10B Wnt family member 10B
Displaying 1 entry
Gene ID Gene Symbol Description Source
22410 Wnt10b wingless-type MMTV integration site family, member 10B
Displaying 1 entry
Gene ID Gene Symbol Description Source
30308 wnt10b wingless-type MMTV integration site family, member 10b
Displaying 1 entry
Gene ID Gene Symbol Description Source
171994 lin-44 Abnormal cell lineage protein 44
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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