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About:
fibular hypoplasia and complex brachydactyly
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An Entity of Type :
owl:Class
, within Data Space :
linkeddata.uriburner.com:28898
associated with source
document(s)
New Facet based on Instances of this Class
Attributes
Values
type
Class
subClassOf
autosomal recessive disease
bone development disease
nodeID://b50937593
nodeID://b50937594
label
fibular hypoplasia and complex brachydactyly
described by
https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/doid.owl
id
DOID:0050790
created_by
lschriml
creation_date
2013-11-12T12:21:56Z
database_cross_reference
KEGG:H00467
MESH:C537931
OMIM:228900
ORDO:2639
has_exact_synonym
Du Pan syndrome
(en)
has_obo_namespace
disease_ontology
http://purl.obolib...g/obo/IAO_0000115
A bone development disease that is characterised by severe reduction or absence of the fibula and complex brachydactyly.
is
topic
of
Human Disease Ontology
is
annotatedSource
of
nodeID://b50937595
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