Term Name: | short-rib thoracic dysplasia 9 with or without polydactyly |
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Synonyms: | renal dysplasia, retinal pigmentary dystrophy, cerebellar ataxia and skeletal dysplasia, SRTD9 |
Definition: | An asphyxiating thoracic dystrophy that has_material_basis_in homozygous or compound heterozygous mutation in the IFT140 gene on chromosome 16p13. |
Ontology: | Human Disease [DOID:0110097] ( DOID:0110097 ) |