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Medical Subject Headings
Preferred Name | Factor X Deficiency | |
Synonyms |
Factor X Deficiencies Stuart Prower Deficiency Deficiency, Factor Ten Deficiencies, Factor 10 Stuart Prower Factor Deficiency Factor 10 Deficiencies Factor 10 Deficiency Stuart-Prower Deficiency Stuart-Prower Factor Deficiency Deficiency, Factor X Factor Ten Deficiencies Deficiency, Stuart-Prower Deficiency, Stuart-Prower Factor Deficiency, Factor 10 Deficiency, Stuart Prower Factor Deficiencies, Factor Ten Deficiencies, Factor X Ten Deficiencies, Factor Factor Ten Deficiency Deficiency, Stuart Prower |
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Definitions |
Blood coagulation disorder usually inherited as an autosomal recessive trait, though it can be acquired. It is characterized by defective activity in both the intrinsic and extrinsic pathways, impaired thromboplastin time, and impaired prothrombin consumption. |
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ID |
http://purl.bioontology.org/ontology/MESH/D005171 |
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altLabel |
Factor X Deficiencies Stuart Prower Deficiency Deficiency, Factor Ten Deficiencies, Factor 10 Stuart Prower Factor Deficiency Factor 10 Deficiencies Factor 10 Deficiency Stuart-Prower Deficiency Stuart-Prower Factor Deficiency Deficiency, Factor X Factor Ten Deficiencies Deficiency, Stuart-Prower Deficiency, Stuart-Prower Factor Deficiency, Factor 10 Deficiency, Stuart Prower Factor Deficiencies, Factor Ten Deficiencies, Factor X Ten Deficiencies, Factor Factor Ten Deficiency Deficiency, Stuart Prower
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AN |
a blood coag disord
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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
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cui |
C0015519
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DC |
1
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definition |
Blood coagulation disorder usually inherited as an autosomal recessive trait, though it can be acquired. It is characterized by defective activity in both the intrinsic and extrinsic pathways, impaired thromboplastin time, and impaired prothrombin consumption.
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DX |
19910101
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HN |
91(75); was see under HYPOPROTHROMBINEMIAS 1975-90
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Inverse of AQ |
http://purl.bioontology.org/ontology/MESH/Q000097 http://purl.bioontology.org/ontology/MESH/Q000178 http://purl.bioontology.org/ontology/MESH/Q000175 http://purl.bioontology.org/ontology/MESH/Q000628 http://purl.bioontology.org/ontology/MESH/Q000276 http://purl.bioontology.org/ontology/MESH/Q000134 http://purl.bioontology.org/ontology/MESH/Q000139 http://purl.bioontology.org/ontology/MESH/Q000266 http://purl.bioontology.org/ontology/MESH/Q000378 http://purl.bioontology.org/ontology/MESH/Q000517 http://purl.bioontology.org/ontology/MESH/Q000662 http://purl.bioontology.org/ontology/MESH/Q000469 http://purl.bioontology.org/ontology/MESH/Q000151 http://purl.bioontology.org/ontology/MESH/Q000150 http://purl.bioontology.org/ontology/MESH/Q000821 http://purl.bioontology.org/ontology/MESH/Q000191 http://purl.bioontology.org/ontology/MESH/Q000196 http://purl.bioontology.org/ontology/MESH/Q000473 http://purl.bioontology.org/ontology/MESH/Q000145 http://purl.bioontology.org/ontology/MESH/Q000382 http://purl.bioontology.org/ontology/MESH/Q000451 http://purl.bioontology.org/ontology/MESH/Q000453 http://purl.bioontology.org/ontology/MESH/Q000534 http://purl.bioontology.org/ontology/MESH/Q000532 http://purl.bioontology.org/ontology/MESH/Q000503 http://purl.bioontology.org/ontology/MESH/Q000188 http://purl.bioontology.org/ontology/MESH/Q000235 http://purl.bioontology.org/ontology/MESH/Q000201 http://purl.bioontology.org/ontology/MESH/Q000209 http://purl.bioontology.org/ontology/MESH/Q000208 http://purl.bioontology.org/ontology/MESH/Q000601 http://purl.bioontology.org/ontology/MESH/Q000000981 http://purl.bioontology.org/ontology/MESH/Q000652 |
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Machine permutation |
91; was see under HYPOPROTHROMBINEMIAS 1975-90
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MDA |
19990101
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MMR |
20170502
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MN |
C16.320.099.320 C15.378.463.320 C15.378.100.141.320 C15.378.100.100.320
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notation |
D005171
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OL |
search HYPOPROTHROMBINEMIAS 1966-74
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prefLabel |
Factor X Deficiency
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TERMUI |
T015831 T000913556 T015827 T000913553 T015828 T015829 T000913554 T015832 T015830 T000913555
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TH |
NLM (1990) NLM (1975) NLM (1992) UNK (19XX) NLM (2018)
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tui |
T047
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subClassOf |
http://purl.bioontology.org/ontology/MESH/D020147 |
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