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Disease Ontology Browser
short-rib thoracic dysplasia 7 with or without polydactyly (DOID:0110090)
Alliance: disease page
Synonyms: short rib-polydactyly syndrome type V; SRPS5; SRTD7
Alt IDs: OMIM:614091, ICD10CM:Q77.2
Definition: An asphyxiating thoracic dystrophy that has_material_basis_in homozygous or compound heterozygous mutation in the WDR35 gene on chromosome 2p21.1.

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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MGI 6.20
The Jackson Laboratory