Medical Subject Headings / 医学主题词表 - Charcot-Marie-Tooth disease, Type 2B1 - Classes

Preferred Name	Charcot-Marie-Tooth disease, Type 2B1
Synonyms	Charcot-Marie-Tooth Neuropathy, Type 2b1
ID	http://purl.bioontology.org/ontology/MESH/C537990
altLabel	Charcot-Marie-Tooth Neuropathy, Type 2b1 Charcot-Marie-Tooth disease, neuronal, Type 2B1 Charcot-Marie-Tooth Disease, Axonal, Autosomal Recessive, B1 CMT2B1 Charcot-Marie-Tooth disease, axonal, Type 2B1
cui	C1854154
HM	D002607 D000083083
Inverse of RB	0
Mapped to	http://purl.bioontology.org/ontology/MESH/D002607 http://purl.bioontology.org/ontology/MESH/D000083083
MDA	20100825
MeSH Frequency	1
MMR	20200221
notation	C537990
prefLabel	Charcot-Marie-Tooth disease, Type 2B1
SC	3
TERMUI	T744381 T806582 T744379 T744380 T744382 T806581
TH	ORD (2010) OMIM (2013)
tui	T047

Delete	Subject	Author	Type	Created
No notes to display

Mapping To	Ontology	Source
http://purl.obolibrary.org/obo/DOID_0110156	Human Disease Ontology / 人类疾病本体	LOOM
http://purl.obolibrary.org/obo/MONDO_0011569	Mondo Disease Ontology / Mondo疾病本体	LOOM
http://purl.obolibrary.org/obo/MONDO_0011569	Experimental Factor Ontology / 实验性因素本体	LOOM
http://purl.bioontology.org/ontology/OMIM/605588	Online Mendelian Inheritance in Man / 在线人类孟德尔遗传数据库	CUI
http://www.orpha.net/ORDO/Orphanet_98856	Orphanet Rare Disease Ontology / Orphanet罕见病本体	LOOM
http://purl.bioontology.org/ontology/OMIM/150330	Online Mendelian Inheritance in Man / 在线人类孟德尔遗传数据库	CUI