Experimental Factor Ontology

Last uploaded: April 15, 2024

Preferred Name	obsolete_Autosomal dominant Charcot-Marie-Tooth disease type 2
Synonyms	Hereditary motor and sensory neuropathy type 2 Autosomal dominant axonal Charcot-Marie-Tooth disease CMT2
ID	http://www.orpha.net/ORDO/Orphanet_64746
Obsolete	true
database_cross_reference	OMIM:616688 OMIM:616687 OMIM:616625 OMIM:616924 ICD10:G60.0 OMIM:616491
deprecated	true
has_exact_synonym	Hereditary motor and sensory neuropathy type 2 Autosomal dominant axonal Charcot-Marie-Tooth disease CMT2
label	obsolete_Autosomal dominant Charcot-Marie-Tooth disease type 2
obsoleted_in_version	3.41.0
preferred label	obsolete_Autosomal dominant Charcot-Marie-Tooth disease type 2
prefLabel	obsolete_Autosomal dominant Charcot-Marie-Tooth disease type 2
reason_for_obsolescence	Replaced with Mondo term.
term replaced by	http://purl.obolibrary.org/obo/MONDO_0018993
subClassOf	http://www.w3.org/2002/07/owl#Thing

Delete	Subject	Author	Type	Created
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Delete	Mapping To	Ontology	Source
	http://www.orpha.net/ORDO/Orphanet_64746	ORDO	SAME_URI