2009AA MedDRA Spanish Source Information
Counts
(skip to: notes samples)
placeholder
| Term Type |
Description |
Count (MRCONSO.RRF) |
|
LT
|
Lower Level Term |
57556 |
|
MTH_LT
|
MTH Lower Level Term |
31724 |
|
PT
|
Designated preferred name |
18209 |
|
MTH_PT
|
Metathesaurus preferred term |
10083 |
|
OL
|
Non-current Lower Level Term |
9031 |
|
MTH_OL
|
MTH Non-current Lower Level Term |
6270 |
|
HT
|
Hierarchical term |
1688 |
|
MTH_HT
|
MTH Hierarchical term |
985 |
|
HG
|
High Level Group Term |
332 |
|
MTH_HG
|
MTH High Level Group Term |
201 |
|
SMQ
|
Standardised MedDRA Query |
151 |
|
MTH_SMQ
|
Metathesaurus version of Standardised MedDRA Query |
87 |
|
AB
|
Abbreviation in any source vocabulary |
26 |
|
OS
|
System-organ class in the WHO Adverse Reaction Terminology |
26 |
|
MTH_OS
|
MTH System-organ class |
13 |
Notes
- A term type indicates the role an atom plays in its source
- An atom is the smallest unit of naming in a source; that is, a specific string with specific code values and identifiers from a specific source.
- Every atom has a separate row in MRCONSO.RRF. Every atom is assigned a term type.
- Term types are assigned based on source documentation or NLM understanding of the source.
- Sample data are provided for every term type in the source (see below).
- See Appendix B3 for a list of all term type abbreviations and their full names.
- See Appendix B.5 for a list of sources and their associated term types, listed in default order of precedence.
- See Section 2.7.1.3.14 of UMLS Documentation for more information on MRCONSO.RRF.
Sample Data
LT
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| CUI |
AUI |
LUI |
SUI |
SDUI |
CODE |
STR |
| C0016167 |
A6566320 |
L4954491 |
S5641996 |
10002180 |
10002180 |
Úlcera anal |
| C0853517 |
A6518599 |
L4919880 |
S5607384 |
10003196 |
10003196 |
Arteriografía carotídea normal |
| C0236073 |
A6465632 |
L2351509 |
S2787364 |
10008034 |
10008034 |
Infarto cerebeloso |
| C0013261 |
A6560405 |
L4950190 |
S5637695 |
10013799 |
10013799 |
Síndrome de Duane |
| C0013274 |
A6455947 |
L2346539 |
S2782394 |
10034130 |
10034130 |
Conducto arterioso persistente |
| C0427564 |
A6476188 |
L2357449 |
S2793304 |
10035530 |
10035530 |
Recuento normal de plaquetas |
| C0033300 |
A6474186 |
L2356357 |
S2792212 |
10036794 |
10036794 |
Progeria |
| C0854918 |
A6525617 |
L4924766 |
S5612270 |
10046436 |
10046436 |
Cáncer uretral regional |
| C0438220 |
A6459762 |
L2348604 |
S2784459 |
10049191 |
10049191 |
Enzimas anormales eritrocitarias |
MTH_LT
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| CUI |
AUI |
LUI |
SUI |
SDUI |
CODE |
STR |
| C0854839 |
A10300492 |
L2353032 |
S2788887 |
10002452 |
10002452 |
Linfoma angioinmunoblastico de celulas T, recurrente |
| C0853892 |
A10296362 |
L2348973 |
S2784828 |
10007733 |
10007733 |
Estado catabolico |
| C0192871 |
A10293952 |
L2346279 |
S2782134 |
10009879 |
10009879 |
Colectomia total |
| C0153871 |
A10300367 |
L2352894 |
S2788749 |
10024319 |
10024319 |
Leucemia plasmacitica (en remision) |
| C0549634 |
A10318999 |
L2705311 |
S3179369 |
10024588 |
10024588 |
Lipidos anormales |
| C0854642 |
A10307344 |
L2360047 |
S2795902 |
10027415 |
10027415 |
Tratamiento de anormaliad metabolica |
| C0034735 |
A10297171 |
L2349599 |
S2785454 |
10037912 |
10037912 |
Fenomeno de Raynaud |
| C0039437 |
A10296142 |
L2348783 |
S2784638 |
10043183 |
10043183 |
Erupcion dental |
| C0040423 |
A10291126 |
L2343554 |
S2779409 |
10044006 |
10044006 |
Amigdalectomia |
PT
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| CUI |
AUI |
LUI |
SUI |
SDUI |
CODE |
STR |
| C0854362 |
A6449806 |
L2343324 |
S2779179 |
10001642 |
10001642 |
Aldolasa elevada |
| C0266781 |
A6450273 |
L2343595 |
S2779450 |
10001959 |
10001959 |
Amniocentesis anormal |
| C0855613 |
A6518487 |
L4919802 |
S5607306 |
10003000 |
10003000 |
Apolipoproteína B elevada |
| C0860684 |
A6452469 |
L2344766 |
S2780621 |
10005369 |
10005369 |
Bilirrubina no conjugada en sangre |
| C0855670 |
A6456451 |
L2346796 |
S2782651 |
10005434 |
10005434 |
Cromo disminuido en sangre |
| C0021100 |
A6538184 |
L4933792 |
S5621296 |
10006563 |
10006563 |
Impétigo bulloso |
| C0267356 |
A6552415 |
L4944580 |
S5632085 |
10013832 |
10013832 |
Perforación duodenal |
| C0033359 |
A6529569 |
L4927624 |
S5615129 |
10014622 |
10014622 |
Encefalomielitis por rubéola |
| C0153452 |
A6525225 |
L4924499 |
S5612013 |
10017614 |
10017614 |
Cáncer de vesícula biliar |
MTH_PT
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| CUI |
AUI |
LUI |
SUI |
SDUI |
CODE |
STR |
| C0263421 |
A10290655 |
L2343066 |
S2778921 |
10000594 |
10000594 |
Acrodermatitis cronica atrofica |
| C0154587 |
A10306823 |
L2359201 |
S2795056 |
10001296 |
10001296 |
Trastorno de adaptacion con ansiedad |
| C0154034 |
A10319766 |
L2706663 |
S3180721 |
10004406 |
10004406 |
Neoplasia benigna de medula espinal |
| C0194422 |
A10297056 |
L2349482 |
S2785337 |
10005025 |
10005025 |
Extraccion de sonda vesical |
| C0040252 |
A10306566 |
L2358945 |
S2794800 |
10005913 |
10005913 |
Tina corporal |
| C0009592 |
A10294176 |
L2346482 |
S2782337 |
10006112 |
10006112 |
Compresion cerebral |
| C0007868 |
A10295203 |
L2347541 |
S2783396 |
10008263 |
10008263 |
Displasia de cervix |
| C0855408 |
A10302138 |
L2354876 |
S2790731 |
10009763 |
10009763 |
Nivel de factor de coagulacion VII elevado |
| C0268070 |
A10294546 |
L2346976 |
S2782831 |
10010957 |
10010957 |
Deficit de cobre |
OL
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| CUI |
AUI |
LUI |
SUI |
SDUI |
CODE |
STR |
| C0155994 |
A11285733 |
L4954573 |
S5642075 |
10013839 |
10000718 |
Úlcera duodenal aguda con hemorragia, con obstrucción |
| C0857041 |
A11328844 |
L4947956 |
S5635461 |
10017955 |
10000951 |
Reagudización de hemorragia gastrointestinal crónica |
| C0153006 |
A11302954 |
L4945061 |
S5632563 |
10036012 |
10001012 |
Poliomielitis aguda no especificada, virus de la polio de tipo III |
| C0002103 |
A11320344 |
L4948736 |
S5636240 |
10039085 |
10001727 |
Rinitis alérgica, causa no especificada |
| C0003089 |
A11328974 |
L4928963 |
S5616468 |
10002556 |
10002557 |
Espondilitis anquilosante y otras espondilopatías inflamatorias |
| C0157809 |
A11320491 |
L4920069 |
S5607573 |
10003274 |
10003353 |
Artropatía con afectación de otras zonas especificadas, asociada a otras enfermedades víricas |
| C0154055 |
A11303235 |
L4940085 |
S5627589 |
10060999 |
10004366 |
Neoplasia benigna de otras localizaciones especificadas |
| C0153999 |
A11303241 |
L4940125 |
S5627629 |
10061007 |
10004421 |
Neoplasia benigna de útero, parte no especificada |
| C0161351 |
A11286258 |
L4947025 |
S5634530 |
10006803 |
10006657 |
Quemadura (de cualquier grado) que afecta 50-59% de la SC con quemadura de IIIg del 30-39% |
MTH_OL
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| CUI |
AUI |
LUI |
SUI |
SDUI |
CODE |
STR |
| C0271355 |
A12692592 |
L6565981 |
S7655079 |
10047641 |
10000110 |
Paralisis del motor ocular externo |
| C0856428 |
A12690472 |
L6563912 |
S7651770 |
10043242 |
10000440 |
Esguince del tendon de Aquiles |
| C0001175 |
A12695762 |
L2713033 |
S3187093 |
10000565 |
10000562 |
Sindrome de inmunodeficiencia adquirida |
| C0156050 |
A12695772 |
L6569338 |
S7656418 |
10002248 |
10000777 |
Ulcera gastroyeyunal aguda con hemorragia y perforacion, con obstruccion |
| C0157463 |
A12693683 |
L6565696 |
S7652967 |
10038436 |
10001046 |
Insuficiencia renal aguda con parto, con mencion de complicacion postparto |
| C0152505 |
A12691560 |
L6566483 |
S7652785 |
10001980 |
10001921 |
Infeccion amebiana de otras localizaciones |
| C0854893 |
A12691567 |
L6563736 |
S7650391 |
10057700 |
10002478 |
Angiosarcoma no metastasico |
| C0263726 |
A12692638 |
L6565398 |
S7650578 |
10003285 |
10003287 |
Artropatia asociada a trastornos dermatologicos |
| C0157807 |
A12691577 |
L6564575 |
S7650589 |
10003274 |
10003340 |
Artropatia con afectacion de la parte inferior de la pierna, asociada a otras enfermedades viricas |
HT
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| CUI |
AUI |
LUI |
SUI |
SDUI |
CODE |
STR |
| C0947793 |
A6553929 |
L4945644 |
S5633149 |
10014997 |
10014997 |
Procedimientos terapéuticos del epidídimo |
| C0851609 |
A6480373 |
L2359911 |
S2795766 |
10029976 |
10029976 |
Trastornos obstructivos de los conductos biliares (excl neoplasias) |
| C0851610 |
A6553865 |
L4945580 |
S5633085 |
10040862 |
10040862 |
Procedimientos histopatológicos de la piel |
| C0851613 |
A6529418 |
L4927506 |
S5615011 |
10034572 |
10034572 |
Embolismo y trombosis periféricos |
| C0000786 |
A6514803 |
L4917247 |
S5604752 |
10000235 |
10000235 |
Abortos espontáneos |
| C0851641 |
A6457631 |
L2347429 |
S2783284 |
10013929 |
10013929 |
Discinesias y trastornos del movimiento NCOC |
| C0947809 |
A6519429 |
L4920499 |
S5608004 |
10003801 |
10003801 |
Auscultación cardiaca |
| C0851660 |
A6553788 |
L4945530 |
S5633035 |
10029292 |
10029292 |
Problemas visuales neurológicos NCOC |
| C0851665 |
A6559657 |
L4949645 |
S5637150 |
10030952 |
10030952 |
Signos y síntomas ópticos NCOC |
MTH_HT
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| CUI |
AUI |
LUI |
SUI |
SDUI |
CODE |
STR |
| C0851600 |
A10290422 |
L2342837 |
S2778692 |
10000232 |
10000232 |
Aborto no especificado como inducido o espontaneo |
| C0001261 |
A10299342 |
L2351875 |
S2787730 |
10000627 |
10000627 |
Infecciones actinomicoticas |
| C0947813 |
A10303546 |
L2356186 |
S2792041 |
10001357 |
10001357 |
Procedimientos terapeuticos de glandula suprarrenal |
| C0001624 |
A10301808 |
L2354522 |
S2790377 |
10001376 |
10001376 |
Neoplasias de la glandula suprarrenal |
| C0852338 |
A10291297 |
L2343744 |
S2779599 |
10002054 |
10002054 |
Anemia hemolitica por factores mecanicos |
| C0852078 |
A10291364 |
L2343775 |
S2779630 |
10002084 |
10002084 |
Anemias (excl hemoglobinopatias) congenitas |
| C0392788 |
A10300748 |
L2353215 |
S2789070 |
10002412 |
10002412 |
Linfomas angiocentricos |
| C0020506 |
A10309151 |
L2515654 |
S2972340 |
10002700 |
10002700 |
Trastornos por hiperfuncion de la hipofisis anterior |
| C0852354 |
A10307135 |
L2359685 |
S2795540 |
10002982 |
10002982 |
Trastornos de las glandulas apocrinas y ecrinas |
HG
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| CUI |
AUI |
LUI |
SUI |
SDUI |
CODE |
STR |
| C0002994 |
A6450724 |
L2343836 |
S2779691 |
10002426 |
10002426 |
Angioedema y urticaria |
| C0851373 |
A6448898 |
L2342841 |
S2778696 |
10000211 |
10000211 |
Aborto y parto con feto muerto |
| C0947735 |
A6553945 |
L4945660 |
S5633165 |
10025506 |
10025506 |
Procedimientos terapéuticos del tracto genital masculino |
| C0851381 |
A6464319 |
L2350871 |
S2786726 |
10000073 |
10000073 |
Hernias abdominales y otras alteraciones de la pared abdominal |
| C0947737 |
A6563889 |
L4952687 |
S5640192 |
10028393 |
10028393 |
Trastornos musculoesqueléticos y del tejido conectivo NCOC |
| C0015414 |
A6470950 |
L2354630 |
S2790485 |
10030054 |
10030054 |
Neoplasias oculares |
| C0851385 |
A6563608 |
L4952414 |
S5639919 |
10018018 |
10018018 |
Trastornos congénitos del tracto gastrointestinal |
| C0876962 |
A6553942 |
L4945657 |
S5633162 |
10009720 |
10009720 |
Procedimientos terapéuticos del sistema nervioso, cráneo y columna vertebral |
| C0948996 |
A6547889 |
L4940973 |
S5628478 |
10006288 |
10006288 |
Neoplasias benignas de mama (incl pezón) |
MTH_HG
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| CUI |
AUI |
LUI |
SUI |
SDUI |
CODE |
STR |
| C0947766 |
A10291080 |
L2343508 |
S2779363 |
10000546 |
10000546 |
Alteraciones metabolicas NCOC |
| C0947742 |
A10307096 |
L2359622 |
S2795477 |
10001302 |
10001302 |
Trastornos de adaptacion (incl subtipos) |
| C0851444 |
A10295956 |
L2348501 |
S2784356 |
10001708 |
10001708 |
Enfermedades alergicas |
| C0851368 |
A10291366 |
L2343778 |
S2779633 |
10002086 |
10002086 |
Anemias no hemoliticas y depresion medular |
| C0947749 |
A10290998 |
L2343430 |
S2779285 |
10002693 |
10002693 |
Alteracion estructural, deposito o degeneracion anteriores del ojo |
| C0851426 |
A10307144 |
L2359707 |
S2795562 |
10003018 |
10003018 |
Trastornos del apetito y de la nutricion en general |
| C0947734 |
A10303635 |
L2356277 |
S2792132 |
10003184 |
10003184 |
Procedimientos terapeuticos vasculares |
| C0851427 |
A10307129 |
L2359677 |
S2795532 |
10004994 |
10004994 |
Trastornos de la vejiga y del cuello de la vejiga (excl calculos) |
| C0948995 |
A10303548 |
L2356188 |
S2792043 |
10005944 |
10005944 |
Procedimientos terapeuticos de huesos y articulaciones |
SMQ
(return to top)
| CUI |
AUI |
LUI |
SUI |
SDUI |
CODE |
STR |
| C1869007 |
A12695710 |
L6567642 |
S7655461 |
20000002 |
20000002 |
Rabdomiólisis/Miopatía (SMQ) |
| C1869091 |
A12692591 |
L6568142 |
S7652956 |
20000004 |
20000004 |
Insuficiencia cardiaca (SMQ) |
| C1869009 |
A12692552 |
L6566126 |
S7656103 |
20000005 |
20000005 |
Trastornos hepáticos (SMQ) |
| C1869010 |
A12693626 |
L6566127 |
S7656104 |
20000006 |
20000006 |
Trastornos hepáticos posiblemente relacionados con fármacos - Búsqueda exhaustiva (SMQ) |
| C1869011 |
A12696760 |
L6565284 |
S7656105 |
20000007 |
20000007 |
Trastornos hepáticos posiblemente relacionados con fármacos - Sólo reacciones graves (SMQ) |
| C1869014 |
A12697796 |
L6564821 |
S7652578 |
20000010 |
20000010 |
Hepatitis, no infecciosa (SMQ) |
| C1869016 |
A12693628 |
L6565804 |
S7653856 |
20000012 |
20000012 |
Neoplasias hepáticas, benignas (SMQ) |
| C1869017 |
A12695712 |
L6565699 |
S7652973 |
20000013 |
20000013 |
Insuficiencia, fibrosis y cirrosis hepática y otras enferm asociadas con afecciones del hígado (SMQ) |
| C1869018 |
A12691495 |
L6563629 |
S7656038 |
20000014 |
20000014 |
Trastornos congénitos, familiares, neonatales y genéticos del hígado (SMQ) |
MTH_SMQ
(return to top)
| CUI |
AUI |
LUI |
SUI |
SDUI |
CODE |
STR |
| C1869006 |
A12694663 |
L6563616 |
S7655911 |
20000001 |
20000001 |
Torsade de pointes/prologancion del intervalo QT (SMQ) |
| C1869007 |
A12690431 |
L6563563 |
S7655460 |
20000002 |
20000002 |
Rabdomiolisis/Miopatia (SMQ) |
| C1869009 |
A12693625 |
L6563636 |
S7656099 |
20000005 |
20000005 |
Trastornos hepaticos (SMQ) |
| C1869010 |
A12692553 |
L6563637 |
S7656100 |
20000006 |
20000006 |
Trastornos hepaticos posiblemente relacionados con farmacos - Busqueda exhaustiva (SMQ) |
| C1869011 |
A12692554 |
L6569292 |
S7656101 |
20000007 |
20000007 |
Trastornos hepaticos posiblemente relacionados con farmacos - Solo reacciones graves (SMQ) |
| C1869012 |
A12693627 |
L6568787 |
S7651845 |
20000008 |
20000008 |
Exploraciones complementarias, signos y sintomas relacionados con el higado (SMQ) |
| C1869013 |
A12690432 |
L6565439 |
S7650891 |
20000009 |
20000009 |
Colestasis e ictericia de origen hepatico (SMQ) |
| C1869015 |
A12695711 |
L6569025 |
S7653855 |
20000011 |
20000011 |
Neoplasias hepaticas, malignas y no especificadas (SMQ) |
| C1869016 |
A12694667 |
L6565007 |
S7653854 |
20000012 |
20000012 |
Neoplasias hepaticas, benignas (SMQ) |
AB
(return to top)
| CUI |
AUI |
LUI |
SUI |
SDUI |
CODE |
STR |
| C0851353 |
A14227007 |
L7592935 |
S8789847 |
10005329 |
10005329 |
Blood |
| C0018799 |
A14227567 |
L7592681 |
S8789883 |
10007541 |
10007541 |
Card |
| C0851352 |
A14227568 |
L7592529 |
S8789932 |
10010331 |
10010331 |
Cong |
| C0851354 |
A14226143 |
L7592414 |
S8790076 |
10013993 |
10013993 |
Ear |
| C0014130 |
A14227008 |
L7593094 |
S8790090 |
10014698 |
10014698 |
Endo |
| C0015397 |
A14227287 |
L6807107 |
S7930338 |
10015919 |
10015919 |
Eye |
| C0017178 |
A14227288 |
L7592727 |
S8790197 |
10017947 |
10017947 |
Gastr |
| C0851362 |
A14225823 |
L7592306 |
S8790198 |
10018065 |
10018065 |
Genrl |
| C0267792 |
A14227851 |
L7592986 |
S8790215 |
10019805 |
10019805 |
Hepat |
OS
(return to top)
| CUI |
AUI |
LUI |
SUI |
SDUI |
CODE |
STR |
| C1261322 |
A6461292 |
L2349383 |
S2785238 |
10022891 |
10022891 |
Exploraciones complementarias |
| C0018799 |
A6480007 |
L2359545 |
S2795400 |
10007541 |
10007541 |
Trastornos cardiacos |
| C0851352 |
A6563622 |
L4952428 |
S5639933 |
10010331 |
10010331 |
Trastornos congénitos, familiares y genéticos |
| C0851353 |
A6563679 |
L4952482 |
S5639987 |
10005329 |
10005329 |
Trastornos de la sangre y del sistema linfático |
| C0027765 |
A6480232 |
L2359768 |
S2795623 |
10029205 |
10029205 |
Trastornos del sistema nervioso |
| C0015397 |
A6480375 |
L2359913 |
S2795768 |
10015919 |
10015919 |
Trastornos oculares |
| C0851354 |
A6563776 |
L4952577 |
S5640082 |
10013993 |
10013993 |
Trastornos del oído y del laberinto |
| C0851355 |
A6563946 |
L4952744 |
S5640249 |
10038738 |
10038738 |
Trastornos respiratorios, torácicos y mediastínicos |
| C0017178 |
A6480290 |
L2359825 |
S2795680 |
10017947 |
10017947 |
Trastornos gastrointestinales |
MTH_OS
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| CUI |
AUI |
LUI |
SUI |
SDUI |
CODE |
STR |
| C0851353 |
A10307128 |
L2359671 |
S2795526 |
10005329 |
10005329 |
Trastornos de la sangre y del sistema linfatico |
| C0851352 |
A10307094 |
L2359620 |
S2795475 |
10010331 |
10010331 |
Trastornos congenitos, familiares y geneticos |
| C0851354 |
A10307168 |
L2359761 |
S2795616 |
10013993 |
10013993 |
Trastornos del oido y del laberinto |
| C0851362 |
A10307201 |
L2359830 |
S2795685 |
10018065 |
10018065 |
Trastornos generales y alteraciones en el lugar de administracion |
| C0021053 |
A10307171 |
L2359767 |
S2795622 |
10021428 |
10021428 |
Trastornos del sistema inmunologico |
| C0947733 |
A10300236 |
L2352827 |
S2788682 |
10022117 |
10022117 |
Lesiones traumaticas, intoxicaciones y complicaciones de procedimientos terapeuticos |
| C0851358 |
A10307157 |
L2359743 |
S2795598 |
10027433 |
10027433 |
Trastornos del metabolismo y de la nutricion |
| C0263660 |
A10307238 |
L2359897 |
S2795752 |
10028395 |
10028395 |
Trastornos musculoesqueleticos y del tejido conjuntivo |
| C0027651 |
A10301801 |
L2354507 |
S2790362 |
10029104 |
10029104 |
Neoplasias benignas, malignas y no especificadas (incl quistes y polipos) |
Last reviewed: 05 May 2009
Last updated: 05 May 2009
First published: 05 May 2009
Metadata| Permanence level: Permanence Not Guaranteed