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Disease Ontology Browser
short-rib thoracic dysplasia 9 with or without polydactyly (DOID:0110097)
Synonyms: renal dysplasia, retinal pigmentary dystrophy, cerebellar ataxia and skeletal dysplasia; SRTD9
Alt IDs: OMIM:266920, ICD10CM:Q87.5
Definition: A short-rib thoracic dysplasia 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 Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
04/18/2017
MGI 6.08
The Jackson Laboratory