Search Ontology:
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
-
- GARD:5478
- ICD10CM:Q76.3
- MIM:601216
- ORDO:2899
- Ontology
- Human Disease ( DOID:0090143 )
- is a type of
-
Other Pages
Genes Involved
Zebrafish Models