Preferred Name |
Factor V Deficiency |
Synonyms |
Disease, Owren |
Definitions |
A deficiency of blood coagulation factor V (known as proaccelerin or accelerator globulin or labile factor) leading to a rare hemorrhagic tendency known as Owren's disease or parahemophilia. It varies greatly in severity. Factor V deficiency is an autosomal recessive trait. (Dorland, 27th ed) |
ID |
http://purl.bioontology.org/ontology/MESH/D005166 |
altLabel |
Disease, Owren Deficiencies, Factor Five Owren Parahemophilia Owrens Disease Factor Five Deficiencies Owren Disease Deficiency, Factor Five Parahemophilias Deficiencies, Labile Factor Labile Factor Deficiency Factor 5 Deficiency Deficiency, Factor V Parahemophilia, Owren Factor Five Deficiency Labile Factor Deficiencies Deficiencies, Factor 5 Deficiency, Factor 5 Disease, Owren's Parahemophilia Factor 5 Deficiencies Owren's Disease Deficiencies, Factor V Factor V Deficiencies Deficiency, Labile Factor |
AN |
a blood coag disord |
AQL |
BL CF CI CL CN CO DG DH DI DT EC EH EM EN EP ET GE HI IM ME MI MO NU PA PC PP PS PX RH RT SU TH UR VE VI |
cui |
C0015499 |
DC |
1 |
definition |
A deficiency of blood coagulation factor V (known as proaccelerin or accelerator globulin or labile factor) leading to a rare hemorrhagic tendency known as Owren's disease or parahemophilia. It varies greatly in severity. Factor V deficiency is an autosomal recessive trait. (Dorland, 27th ed) |
DX |
19730101 |
HN |
73(64); was see under HYPOPROTHROMBINEMIAS 1963-72 |
Inverse of AQ |
http://purl.bioontology.org/ontology/MESH/Q000401 http://purl.bioontology.org/ontology/MESH/Q000150 http://purl.bioontology.org/ontology/MESH/Q000188 http://purl.bioontology.org/ontology/MESH/Q000517 http://purl.bioontology.org/ontology/MESH/Q000201 http://purl.bioontology.org/ontology/MESH/Q000145 http://purl.bioontology.org/ontology/MESH/Q000503 http://purl.bioontology.org/ontology/MESH/Q000453 http://purl.bioontology.org/ontology/MESH/Q000208 http://purl.bioontology.org/ontology/MESH/Q000134 http://purl.bioontology.org/ontology/MESH/Q000821 http://purl.bioontology.org/ontology/MESH/Q000382 http://purl.bioontology.org/ontology/MESH/Q000601 http://purl.bioontology.org/ontology/MESH/Q000235 http://purl.bioontology.org/ontology/MESH/Q000523 http://purl.bioontology.org/ontology/MESH/Q000276 http://purl.bioontology.org/ontology/MESH/Q000191 http://purl.bioontology.org/ontology/MESH/Q000652 http://purl.bioontology.org/ontology/MESH/Q000662 http://purl.bioontology.org/ontology/MESH/Q000151 http://purl.bioontology.org/ontology/MESH/Q000628 http://purl.bioontology.org/ontology/MESH/Q000196 http://purl.bioontology.org/ontology/MESH/Q000534 http://purl.bioontology.org/ontology/MESH/Q000266 http://purl.bioontology.org/ontology/MESH/Q000532 http://purl.bioontology.org/ontology/MESH/Q000139 http://purl.bioontology.org/ontology/MESH/Q000378 http://purl.bioontology.org/ontology/MESH/Q000175 http://purl.bioontology.org/ontology/MESH/Q000000981 http://purl.bioontology.org/ontology/MESH/Q000097 http://purl.bioontology.org/ontology/MESH/Q000473 http://purl.bioontology.org/ontology/MESH/Q000451 http://purl.bioontology.org/ontology/MESH/Q000209 |
Machine permutation |
73; was see under HYPOPROTHROMBINEMIAS 1963-72 |
Mapped from | |
MDA |
19990101 |
MMR |
20170502 |
MN |
C15.378.463.300 C15.378.100.100.300 C16.320.099.300 C15.378.100.141.300 |
notation |
D005166 |
OL |
use HYPOPROTHROMBINEMIAS to search FACTOR V DEFICIENCY 1966-72 |
prefLabel |
Factor V Deficiency |
TERMUI |
T000913531 T811527 T015789 T015792 T000913528 T015790 T015791 T015788 T811528 T000913530 T000913529 |
TH |
UNK (19XX) NLM (2018) NLM (1964) OMIM (2013) NLM (1999) |
tui |
T047 |
subClassOf |
http://purl.bioontology.org/ontology/MESH/D006474 |