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Metadata
DOID DOID:0050790
Name fibular hypoplasia and complex brachydactyly
Definition An autosomal recessive disease that is characterised by severe reduction or absence of the fibula and complex brachydactyly.
http://omim.org/entry/228900?search=228900&highlight=228900, http://www.orpha.net/consor/cgi-bin/Disease_Search.php?lng=EN&data_id=2413&Disease_Disease_Search_diseaseType=ORPHA&Disease_Disease_Search_diseaseGroup=2639&Disease%28s%29/group%20of%20diseases=Du-Pan-syndrome&title=Du-Pan-syndrome&search=Disease_Search_Simple, https://www.ncbi.nlm.nih.gov/pubmed/16222676
Synonyms

Du Pan syndrome [EXACT]

Xrefs

KEGG:H00467

MESH:C537931

OMIM:228900

Relationships

is_a autosomal recessive disease

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