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short-rib thoracic dysplasia 10 with or without polydactyly (DOID:0110091)
Alliance: disease page
Synonyms: SRTD10
Alt IDs: OMIM:615630, ICD10CM:Q77.2, ICD10CM:Q87.5
Definition: An asphyxiating thoracic dystrophy that has_material_basis_in homozygous or compound heterozygous mutation in the IFT172 gene on chromosome 2p23.

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Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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MGI 6.12
The Jackson Laboratory