Medical Subject Headings / 医学主题词表 - Hypodysfibrinogenemia, Congenital - Classes

Preferred Name	Hypodysfibrinogenemia, Congenital
ID	http://purl.bioontology.org/ontology/MESH/C565970
cui	C1859970
HM	D000347
Inverse of RB	0
Mapped to	http://purl.bioontology.org/ontology/MESH/D000347
MDA	20121105
MeSH Frequency	12
notation	C565970
prefLabel	Hypodysfibrinogenemia, Congenital
SC	3
TERMUI	T807706
TH	OMIM (2013)
tui	T047

Delete	Subject	Author	Type	Created
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Delete	Mapping To	Ontology	Source
	http://purl.bioontology.org/ontology/OMIM/134820	Online Mendelian Inheritance in Man / 在线人类孟德尔遗传数据库	CUI
	http://purl.bioontology.org/ontology/OMIM/616004	Online Mendelian Inheritance in Man / 在线人类孟德尔遗传数据库	CUI