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Disease Ontology Browser
fibular hypoplasia and complex brachydactyly (DOID:0050790)
Alliance: disease page
Synonyms: Du Pan syndrome
Alt IDs: OMIM:228900, KEGG:H00467, MESH:C537931, ORDO:2639
Definition: An autosomal recessive disease that is characterised by severe reduction or absence of the fibula and complex brachydactyly.

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
02/11/2020
MGI 6.14
The Jackson Laboratory