Medical Subject Headings / 医学主题词表

Last uploaded: September 7, 2023
Preferred Name

Charcot-Marie-Tooth disease, Type 2B

Synonyms

HMSN IIB

ID

http://purl.bioontology.org/ontology/MESH/C537989

altLabel

HMSN IIB

CMT2B

CMT 2B

Charcot-Marie-Tooth disease, axonal, Type 2B

Hereditary motor and sensory neuropathy 2 B (HMSN 2 B)

Peripheral sensory neuropathy, autosomal dominant (PSN)

Hereditary Motor And Sensory Neuropathy IIB

HMSN2B

Charcot-Marie-Tooth disease, neuronal, Type 2B

Charcot-Marie-Tooth Neuropathy, Type 2B

Charcot-Marie-Tooth Disease, Autosomal Dominant, Type 2B

cui

C1833219

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

18

MMR

20200228

notation

C537989

prefLabel

Charcot-Marie-Tooth disease, Type 2B

SC

3

TERMUI

T744378

T823375

T823376

T823374

T744373

T744375

T823372

T828165

T744377

T823373

T823377

T744376

TH

NLM (2013)

ORD (2010)

OMIM (2013)

tui

T047

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http://purl.bioontology.org/ontology/OMIM/602298 Online Mendelian Inheritance in Man / 在线人类孟德尔遗传数据库 CUI
http://purl.bioontology.org/ontology/OMIM/600882 Online Mendelian Inheritance in Man / 在线人类孟德尔遗传数据库 CUI
http://purl.obolibrary.org/obo/DOID_0110159 Human Disease Ontology / 人类疾病本体 LOOM
http://purl.obolibrary.org/obo/MONDO_0010949 Mondo Disease Ontology / Mondo疾病本体 LOOM
http://purl.obolibrary.org/obo/MONDO_0010949 Experimental Factor Ontology / 实验性因素本体 LOOM