FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term syndactyly type 4 ID (Ontology) DOID:0111818 (Human Disease)
Definition A syndactyly characterized by complete bilateral syndactyly involving all digits 1 to 5 that has_material_basis_in heterozygous mutation of a SHH regulatory element in intron 5 of the LMBR1 gene on chromosome 7q36.3.
Also Known As "Haas type syndactyly" ; "polysyndactyly, Haas type" ; "SDTY4"
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 Genes
 syndactyly type 4       1
 for disease ribbon | syndactyly type 4       1
 model of | syndactyly type 4       1
Spanning Tree (Parents/Children)
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autosomal genetic disease
 |__autosomal dominant disease__
synostosis                      |
 |__syndactyly__________________|
                                syndactyly type 4  1 rec.
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Is a autosomal dominant disease
syndactyly
Part of
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Synonyms
  • "Haas type syndactyly" EXACT
    "polysyndactyly, Haas type" EXACT
    "SDTY4" EXACT OMO:0003012
Secondary IDs
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GARD:4434
MESH:C566092
MIM:186200
ORDO:93405
SNOMEDCT_US_2023_03_01:719158007
UMLS_CUI:C1861355