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DO Term : lacrimoauriculodentodigital syndrome 3 [DOID:0081372] Disease Ontology

Namespace  disease_ontology Obsolete  false
description  A LADD syndrome that is characterized by aplasia, atresia or hypoplasia of the lacrimal and salivary systems, cup-shaped ears, hearing loss, and dental and digital anomalies and that has_material_basis_in heterozygous mutation in the FGF10 gene on chromosome 5p12.
  • synonyms:
  • 620193,
  • Lacrimo-auriculo-dento-digital syndrome 3,
  • OMIM:620193
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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