About: nemaline myopathy

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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	congenital structural myopathy nodeID://b50951642
label	nemaline myopathy
comment	Xref MGI.
described by	https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/doid.owl
id	DOID:3191
database_cross_reference	GARD:12033 ICD10CM:G71.21 MESH:D017696 OMIM:PS161800 ORDO:607 SNOMEDCT_US_2021_09_01:75072002 UMLS_CUI:C0206157
has_exact_synonym	Nemaline body disease (en) nemaline rod myopathy (en) rod myopathy (en)
has_obo_namespace	disease_ontology
in_subset	DO_FlyBase_slim DO_rare_slim
http://purl.obolib...g/obo/IAO_0000115	A congenital structural myopathy characterized by generally non-progressive muscle weakness of varying severity; certain muscle fibers show the presence of rod-like structures called nemaline bodies.
is subClassOf of	nemaline myopathy 1 nemaline myopathy 3 nemaline myopathy 2 nemaline myopathy 9 nemaline myopathy 8 nemaline myopathy 10 nemaline myopathy 4 nemaline myopathy 11 nemaline myopathy 7 nemaline myopathy 6 nemaline myopathy 5
is topic of	Human Disease Ontology
is annotatedSource of	nodeID://b50951643

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