Medical Subject Headings

Last uploaded: November 5, 2019
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Preferred Name

Hyperheparinemia
ID

http://purl.bioontology.org/ontology/MESH/C562723
cui

C3203346
HM

D001778
Inverse of RB

0
Mapped to

http://purl.bioontology.org/ontology/MESH/D001778
MDA

20121105
MeSH Frequency

16
MMR

20160929
notation

C562723
prefLabel

Hyperheparinemia
SC

3
Scope Statement

A congenital susceptibility to hemmorhage due to an excess of clotting inhibitor. The blood clotting defected may be corrected in vitro by PROTAMINE SULFATE and TOLUIDINE BLUE. OMIM: 144050
TERMUI

T801375
TH

OMIM (2013)
tui

T047
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Delete Mapping To Ontology Source
http://purl.bioontology.org/ontology/OMIM/144050 Online Mendelian Inheritance in Man CUI
http://purl.bioontology.org/ontology/OMIM/144050 Online Mendelian Inheritance in Man LOOM
http://purl.bioontology.org/ontology/ICD10CM/D68.32 International Classification of Diseases, Version 10 - Clinical Modification CUI