About: Charcot-Marie-Tooth disease type 3

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

OMIM mapping confirmed by DO. [SN].

Attributes	Values
type	Class
subClassOf	autosomal dominant disease autosomal recessive disease Charcot-Marie-Tooth disease nodeID://b50937083 nodeID://b50937084
label	Charcot-Marie-Tooth disease type 3
comment	OMIM mapping confirmed by DO. [SN].
described by	https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/doid.owl
id	DOID:0050540
database_cross_reference	OMIM:145900
has_exact_synonym	DEJERINE-SOTTAS NEUROPATHY (en) DEJERINE-SOTTAS SYNDROME (en)
has_obo_namespace	disease_ontology
http://purl.obolib...g/obo/IAO_0000115	A Charcot-Marie-Tooth disease that is characterized by motor and sensory peripheral neuropathies caused by demyelination.
is topic of	Human Disease Ontology
is annotatedSource of	nodeID://b50937085

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