FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term split hand-foot malformation 6 ID (Ontology) DOID:0090026 (Human Disease)
Definition A split-hand/foot malformation that has_material_basis_in homozygous mutation in the WNT10B gene on chromosome 12q13.
Also Known As "SHFM6"
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DO.org
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 Genes
 split hand-foot malformation 6       1
 for disease ribbon | split hand-foot malformation 6       1
 model of | split hand-foot malformation 6       1
Spanning Tree (Parents/Children)
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autosomal genetic disease
 |__autosomal recessive disease___
bone development disease          |
 |__split hand-foot malformation__|
                                  split hand-foot malformation 6  1 rec.
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Is a autosomal recessive disease
split hand-foot malformation
Part of
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Synonyms
  • "SHFM6" EXACT OMO:0003012
Secondary IDs
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MESH:C574275
MIM:225300
NCI:C75000
ORDO:2440
SNOMEDCT_US_2023_03_01:81208006
UMLS_CUI:C0265554