Medical Subject Headings / 医学主题词表

Last uploaded: September 7, 2023

Preferred Name	Brachydactyly type A2
Synonyms	Mohr-Wriedt type brachydactyly
ID	http://purl.bioontology.org/ontology/MESH/C537089
altLabel	Mohr-Wriedt type brachydactyly Brachymesophalangy Ii Brachydactyly, Type A2 Brachymesophalangy 2
cui	C1832702
HM	D059327
Inverse of RB	0
Mapped to	http://purl.bioontology.org/ontology/MESH/D059327
MDA	20100825
MeSH Frequency	4
MMR	20120824
notation	C537089
prefLabel	Brachydactyly type A2
SC	3
TERMUI	T741421 T802781 T741419 T741420 T802782
TH	ORD (2010) OMIM (2013)
tui	T019

Delete	Subject	Author	Type	Created
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Mapping To	Ontology	Source
http://purl.obolibrary.org/obo/MONDO_0007216	Mondo Disease Ontology / Mondo疾病本体	LOOM
http://purl.obolibrary.org/obo/MONDO_0007216	Experimental Factor Ontology / 实验性因素本体	LOOM
http://purl.bioontology.org/ontology/OMIM/112261	Online Mendelian Inheritance in Man / 在线人类孟德尔遗传数据库	CUI
http://purl.obolibrary.org/obo/DOID_0110965	Human Disease Ontology / 人类疾病本体	LOOM
http://purl.bioontology.org/ontology/OMIM/601146	Online Mendelian Inheritance in Man / 在线人类孟德尔遗传数据库	CUI
http://purl.bioontology.org/ontology/OMIM/112600	Online Mendelian Inheritance in Man / 在线人类孟德尔遗传数据库	CUI
http://purl.bioontology.org/ontology/OMIM/112600	Online Mendelian Inheritance in Man / 在线人类孟德尔遗传数据库	LOOM
http://www.orpha.net/ORDO/Orphanet_93396	Orphanet Rare Disease Ontology / Orphanet罕见病本体	LOOM
http://purl.bioontology.org/ontology/OMIM/603248	Online Mendelian Inheritance in Man / 在线人类孟德尔遗传数据库	CUI