About: split hand-foot malformation 1

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An Entity of Type : owl:Class, within Data Space : linkeddata.uriburner.com:28898 associated with source document(s)

Attributes	Values
type	Class
subClassOf	autosomal dominant disease split hand-foot malformation nodeID://b50942071 nodeID://b50942072
label	split hand-foot malformation 1
described by	https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/doid.owl
id	DOID:0090021
database_cross_reference	ICD10CM:Q71.6 OMIM:183600 ORDO:2440
has_exact_synonym	SHFD1 (en) SHFM1 (en)
has_obo_namespace	disease_ontology
http://purl.obolib...g/obo/IAO_0000115	A split-hand/foot malformation that has_material_basis_in contiguous gene mutations caused by deletion, duplication, or rearrangement of chromosome 7q21.3 involving the DSS1, DLX5, and DLX6 genes and possible regulatory elements in the region.
is topic of	Human Disease Ontology
is annotatedSource of	nodeID://b50942076

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