About   Help   FAQ
Disease Ontology Browser
short-rib thoracic dysplasia 9 with or without polydactyly (DOID:0110097)
Alliance: disease page
Synonyms: renal dysplasia, retinal pigmentary dystrophy, cerebellar ataxia and skeletal dysplasia; SRTD9
Alt IDs: OMIM:266920, ICD10CM:Q87.5
Definition: An asphyxiating thoracic dystrophy that has_material_basis_in homozygous or compound heterozygous mutation in the IFT140 gene on chromosome 16p13.

Disease References using Mouse Models (1)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB), Gene Ontology (GO)
Citing These Resources
Funding Information
Warranty Disclaimer & Copyright Notice
Send questions and comments to User Support.
last database update
MGI 6.20
The Jackson Laboratory