About: iridogoniodysgenesis syndrome

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

Xref MGI.

Attributes	Values
type	Class
subClassOf	autosomal dominant disease iris disease nodeID://b50937583
label	iridogoniodysgenesis syndrome
comment	Xref MGI.
described by	https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/doid.owl
id	DOID:0050786
created_by	lschriml
creation_date	2013-11-12T10:28:51Z
database_cross_reference	OMIM:137600 OMIM:601631 ORDO:98634
has_exact_synonym	IGDS (en) IRID 1 (en) IRID 2 (en) iridogoniodysgenesis type 1 (en) iridogoniodysgenesis type 2 (en)
has_obo_namespace	disease_ontology
in_subset	DO_rare_slim
http://purl.obolib...g/obo/IAO_0000115	An iris disease that is characterized by the iris stroma being hypoplastic resulting from abnormalities in the differentiation of the anterior segment structures and increased values of intraocular pressure and has_material_basis_in autosomal dominant inheritance of mutations in the PITX2 gene.
is topic of	Human Disease Ontology
is annotatedSource of	nodeID://b50937584

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