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Human Disease

brachyolmia-amelogenesis imperfecta syndrome

Term ID
DOID:0090143
Synonyms
  • DASS
  • dental anomalies and short stature
  • platyspondyly with amelogenesis imperfecta
  • selective tooth agenesis 5
  • STHAG6
Definition
A syndrome characterized by skeletal dysplasia (broad ilia, elongated femoral necks with coxa valga, scoliosis), mild platyspondyly, short trunked short stature, and amelogenesis imperfecta that has_material_basis_in autosomal recessive inheritance of homozygous or compound heterozygous mutation in the latent transforming growth factor beta binding protein 3 gene (LTBP3) on chromosome 11q13. (2)
References
Ontology
Human Disease   ( DOID:0090143 )
Relationships
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Genes Involved
Zebrafish Models