About: congenital muscular dystrophy merosin-positive

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About: congenital muscular dystrophy merosin-positive 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	congenital muscular dystrophy autosomal recessive disease nodeID://b50943347 nodeID://b50943348 nodeID://b50943349
label	congenital muscular dystrophy merosin-positive
described by	https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/doid.owl
id	DOID:0110638
database_cross_reference	OMIM:609456
has_obo_namespace	disease_ontology
http://purl.obolib...g/obo/IAO_0000115	A congenital muscular dystrophy characterized by autosomal recessive inheritance of generalized muscle weakness and hypotonia without arthrogryposis or central nervous system involvement that has_material_basis_in mutation in the chromosome region 4p16.3.
is topic of	Human Disease Ontology
is annotatedSource of	nodeID://b50943350

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