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DO Term : tetraamelia syndrome 1 [DOID:0112192] Disease Ontology

Namespace  disease_ontology Obsolete  false
description  A tetraamelia syndrome characterized by complete limb agenesis without defects of scapulae or clavicles that has_material_basis_in homozygous or compound heterozygous mutation in WNT3 on chromosome 17q21.31-q21.32.
  • synonyms:
  • OMIM:273395,
  • GARD:5148,
  • TETAMS1,
  • 273395,
  • tetra-amelia syndrome 1
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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