About: mandibulofacial dysostosis, Guion-Almeida type

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About: mandibulofacial dysostosis, Guion-Almeida type Goto Sponge NotDistinct Permalink

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 syndrome nodeID://b50940559
label	mandibulofacial dysostosis, Guion-Almeida type (en)
described by	https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/doid.owl
id	DOID:0080196
database_cross_reference	GARD:10056 OMIM:610536 ORDO:79113
has_exact_synonym	MFDM syndrome (en) mandibulofacial dysostosis with microcephaly (en) mandibulofacial dysostosis-microcephaly syndrome (en)
has_obo_namespace	disease_ontology
in_subset	DO_rare_slim
http://purl.obolib...g/obo/IAO_0000115	A syndrome characterized by progressive microcephaly, micrognathia, microtia, dysplastic ears, preauricular skin tags, speech delay, significant developmental delay, midface and malar hypoplasia.
is topic of	Human Disease Ontology
is annotatedSource of	nodeID://b50940560

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