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DO Term : syndactyly type 4 [DOID:0111818] Disease Ontology

Namespace  disease_ontology Obsolete  false
description  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.
  • synonyms:
  • UMLS_CUI:C1861355,
  • SNOMEDCT_US_2023_03_01:719158007,
  • Haas type syndactyly,
  • ORDO:93405,
  • OMIM:186200,
  • polysyndactyly, Haas type,
  • MESH:C566092,
  • GARD:4434,
  • 186200,
  • SDTY4
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Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents