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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)
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last database update
02/20/2024
MGI 6.23
The Jackson Laboratory