Medical Subject Headings

Last uploaded: November 5, 2019
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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

10
notation

C565970
prefLabel

Hypodysfibrinogenemia, Congenital
SC

3
TERMUI

T807706
TH

OMIM (2013)
tui

T047
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Delete Mapping To Ontology Source
http://purl.bioontology.org/ontology/OMIM/134820 Online Mendelian Inheritance in Man CUI
http://purl.bioontology.org/ontology/OMIM/616004 Online Mendelian Inheritance in Man CUI