Read Codes, Clinical Terms Version 3 (CTV3)

Last uploaded: January 31, 2024

Preferred Name	Hereditary motor and sensory neuropathy type II
Synonyms	Peroneal muscular atrophy of neuronal type
ID	http://purl.bioontology.org/ontology/RCD/X00AA
altLabel	Peroneal muscular atrophy of neuronal type Charcot-Marie-Tooth disease of neuronal type
cui	C0270914
notation	X00AA
prefLabel	Hereditary motor and sensory neuropathy type II
RID	Y00WP Y00WO Y00WQ
tui	T047
subClassOf	http://purl.bioontology.org/ontology/RCD/F3610

Delete	Subject	Author	Type	Created
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Mapping To	Ontology	Source
http://purl.bioontology.org/ontology/MDRGER/10077308	MDRGER	CUI
http://purl.bioontology.org/ontology/MSHFRE/D002607	MSHFRE	CUI
http://purl.bioontology.org/ontology/MESH/D002607	MESH	CUI
http://purl.bioontology.org/ontology/MDRFRE/10077308	MDRFRE	CUI
http://purl.bioontology.org/ontology/SCTSPA/398187000	SCTSPA	CUI
http://purl.bioontology.org/ontology/MEDDRA/10077308	MEDDRA	CUI
http://purl.bioontology.org/ontology/SNMI/DA-44032	SNMI	CUI
http://purl.bioontology.org/ontology/SNOMEDCT/398187000	SNOMEDCT	CUI
http://purl.bioontology.org/ontology/SNMI/DA-44025	SNMI	CUI
http://purl.bioontology.org/ontology/RCTV2/F368100	RCTV2	LOOM