Lista över MeSH-koder (C15)
Följande är en ofullständig lista över "C"-koderna för medicinska ämnesrubriker (MeSH), enligt definition av United States National Library of Medicine (NLM).
Denna lista fortsätter informationen på Lista över MeSH-koder (C14) . Koder som följer dessa finns i Lista över MeSH-koder (C16) . För andra MeSH-koder, se Lista över MeSH-koder .
Källan för detta innehåll är uppsättningen 2006 MeSH Trees från NLM.
MeSH C15 – hemiska och lymfatiska sjukdomar
MeSH C15.378 – hematologiska sjukdomar
MeSH C15.378.071 – anemi
- MeSH C15.378.071.085 – anemi, aplastisk
- MeSH C15.378.071.085.080 – anemi, hypoplastisk, medfödd
- MeSH C15.378.071.085.080.090 – anemi, diamond-blackfan
- MeSH C15.378.071.085.080.280 – fanconi-anemi
- MeSH C15.378.071.141 – anemi, hemolytisk
- MeSH C15.378.071.141.125 – anemi, hemolytisk, autoimmun
- MeSH C15.378.071.141.150 – anemi, hemolytisk, medfödd
- MeSH C15.378.071.141.150.095 – anemi, dyserytropoetisk, medfödd
- MeSH C15.378.071.141.150.100 – anemi, hemolytisk, medfödd icke-sfärocytisk
- MeSH C15.378.071.141.150.150 – anemi, sicklecell
- MeSH C15.378.071.141.150.150.440 – hemoglobin sc sjukdom
- MeSH C15.378.071.141.150.150.670 – sicklecellsdrag
- MeSH C15.378.071.141.150.365 – elliptocytos, ärftlig
- MeSH C15.378.071.141.150.480 – glukosfosfatdehydrogenasbrist
- MeSH C15.378.071.141.150.480.370 – favism
- MeSH C15.378.071.141.150.490 – hemoglobin c-sjukdom
- MeSH C15.378.071.141.150.785 – sfärocytos, ärftlig
- MeSH C15.378.071.141.150.875 – talassemi
- MeSH C15.378.071.141.150.875.100 – alfa-talassemi
- MeSH C15.378.071.141.150.875.150 – beta-talassemi
- MeSH C15.378.071.141.370 – favism
- MeSH C15.378.071.141.510 – hemoglobinuri
- MeSH C15.378.071.141.510.460 – hemoglobinuri, paroxysmal
- MeSH C15.378.071.141.610 – hemolytiskt-uremiskt syndrom
- MeSH C15.378.071.196 – anemi, hypokromisk
- MeSH C15.378.071.196.300 – anemi, järnbrist
- MeSH C15.378.071.252 – anemi, makrocytisk
- MeSH C15.378.071.252.196 – anemi, megaloblastisk
- MeSH C15.378.071.252.196.500 – anemi, perniciös
- MeSH C15.378.071.307 – anemi, myeloftisk
- MeSH C15.378.071.363 – anemi, neonatal
- MeSH C15.378.071.363.344 – fetofetal transfusion
- MeSH C15.378.071.363.511 – fostertransfusion
- MeSH C15.378.071.400 – anemi, refraktär
- MeSH C15.378.071.400.080 – anemi, refraktär, med överskott av blaster
- MeSH C15.378.071.419 – anemi, sideroblastisk
- MeSH C15.378.071.750 – aplasi av röda blodkroppar, ren
- MeSH C15.378.071.750.500 – anemi, diamond-blackfan
MeSH C15.378.100 – blodkoagulationsrubbningar
- MeSH C15.378.100.141 – koagulationsproteinstörningar
- MeSH C15.378.100.141.036 – aktiverat protein c-resistens
- MeSH C15.378.100.141.072 – afibrinogenemi
- MeSH C15.378.100.141.300 – faktor v-brist
- MeSH C15.378.100.141.310 – faktor vii-brist
- MeSH C15.378.100.141.320 – faktor x brist
- MeSH C15.378.100.141.325 – faktor xi-brist
- MeSH C15.378.100.141.330 – faktor xii-brist
- MeSH C15.378.100.141.335 – faktor xiii-brist
- MeSH C15.378.100.141.500 – hemofili a
- MeSH C15.378.100.141.510 – hemofili b
- MeSH C15.378.100.141.550 – hypoprotrombinemier
- MeSH C15.378.100.141.900 – von willebrands sjukdom
- MeSH C15.378.100.220 – disseminerad intravaskulär koagulation
- MeSH C15.378.100.425 – blodkoagulationsrubbningar, ärftliga
- MeSH C15.378.100.425.037 – aktiverat protein c-resistens
- MeSH C15.378.100.425.056 – afibrinogenemi
- MeSH C15.378.100.425.075 – antitrombin iii-brist
- MeSH C15.378.100.425.080 – bernard-souliers syndrom
- MeSH C15.378.100.425.300 – faktor v-brist
- MeSH C15.378.100.425.310 – faktor vii-brist
- MeSH C15.378.100.425.320 – faktor x brist
- MeSH C15.378.100.425.325 – faktor xi-brist
- MeSH C15.378.100.425.330 – faktor xii-brist
- MeSH C15.378.100.425.335 – faktor xiii-brist
- MeSH C15.378.100.425.500 – hemofili a
- MeSH C15.378.100.425.510 – hemofili b
- MeSH C15.378.100.425.515 – hermanski-pudlak syndrom
- MeSH C15.378.100.425.550 – hypoprotrombinemier
- MeSH C15.378.100.425.690 – protein c-brist
- MeSH C15.378.100.425.820 – trombasteni
- MeSH C15.378.100.425.900 – von willebrands sjukdom
- MeSH C15.378.100.425.970 – wiskott-aldrichs syndrom
- MeSH C15.378.100.685 – brist på trombocytlagringspool
- MeSH C15.378.100.685.400 – hermanski-pudlak syndrom
- MeSH C15.378.100.800 – proteinbrist
- MeSH C15.378.100.802 – purpura
- MeSH C15.378.100.802.250 – purpura, hyperglobulinemisk
- MeSH C15.378.100.802.375 – purpura, schoenlein-henoch
- MeSH C15.378.100.802.500 – purpura, trombocytopenisk
- MeSH C15.378.100.805 – purpura, trombocytopenisk
- MeSH C15.378.100.805.600 – purpura, trombocytopenisk, idiopatisk
- MeSH C15.378.100.805.680 – purpura, trombotisk trombocytopenisk
- MeSH C15.378.100.805.972 – wiskott-aldrichs syndrom
- MeSH C15.378.100.832 – trombocytemi, hemorragisk
- MeSH C15.378.100.920 – K-vitaminbrist
- MeSH C15.378.100.920.360 – hemorragisk sjukdom hos nyfödda
MeSH C15.378.120 – blodgruppsinkompatibilitet
- MeSH C15.378.120.413 – erytroblastos, foster
- MeSH C15.378.120.413.480 – hydrops fetalis
- MeSH C15.378.120.413.502 – kernicterus
- MeSH C15.378.120.780 – rh isoimmunisering
MeSH C15.378.140 – blodplättsrubbningar
- MeSH C15.378.140.120 – bernard-souliers syndrom
- MeSH C15.378.140.735 – brist på trombocytlagringspool
- MeSH C15.378.140.735.400 – hermanski-pudlak syndrom
- MeSH C15.378.140.810 – trombasteni
- MeSH C15.378.140.855 – trombocytopeni
- MeSH C15.378.140.855.313 – hemolytiskt-uremiskt syndrom
- MeSH C15.378.140.855.700 – purpura, trombocytopenisk
- MeSH C15.378.140.855.700.600 – purpura, trombocytopen, idiopatisk
- MeSH C15.378.140.855.700.680 – purpura, trombotisk trombocytopenisk
- MeSH C15.378.140.855.700.972 – wiskott-aldrichs syndrom
- MeSH C15.378.140.860 – trombocytos
- MeSH C15.378.140.860.800 – trombocytemi, hemorragisk
- MeSH C15.378.140.900 – von willebrands sjukdom
MeSH C15.378.147 – blodproteinrubbningar
- MeSH C15.378.147.068 – abetalipoproteinemi
- MeSH C15.378.147.142 – agammaglobulinemi
- MeSH C15.378.147.150 – antitrombin iii-brist
- MeSH C15.378.147.333 – dysgammaglobulinemi
- MeSH C15.378.147.333.500 – iga-brist
- MeSH C15.378.147.333.750 – igg-brist
- MeSH C15.378.147.542 – hypergammaglobulinemi
- MeSH C15.378.147.542.640 – monoklonala gammopatier, benigna
- MeSH C15.378.147.607 – hypoproteinemi
- MeSH C15.378.147.607.500 – hypoalbuminemi
- MeSH C15.378.147.780 – paraproteinemier
- MeSH C15.378.147.780.243 – kryoglobulinemi
- MeSH C15.378.147.780.490 – tungkedjesjukdom
- MeSH C15.378.147.780.490.512 – immunproliferativ tunntarmssjukdom
- MeSH C15.378.147.780.650 – multipelt myelom
- MeSH C15.378.147.780.750 – diktsyndrom
- MeSH C15.378.147.780.925 – waldenström makroglobulinemi
- MeSH C15.378.147.880 – protein c-brist
- MeSH C15.378.147.890 – proteinbrist
MeSH C15.378.190 – benmärgssjukdomar
- MeSH C15.378.190.196 – anemi, aplastisk
- MeSH C15.378.190.196.080 – anemi, hypoplastisk, medfödd
- MeSH C15.378.190.196.080.090 – anemi, diamond-blackfan
- MeSH C15.378.190.196.080.280 – fanconi-anemi
- MeSH C15.378.190.250 – benmärgsneoplasmer
- MeSH C15.378.190.625 – myelodysplastiska syndrom
- MeSH C15.378.190.625.062 – anemi, refraktär
- MeSH C15.378.190.625.062.080 – anemi, refraktär, med överskott av blaster
- MeSH C15.378.190.625.070 – anemi, sideroblastisk
- MeSH C15.378.190.625.460 – hemoglobinuri, paroxysmal
- MeSH C15.378.190.625.543 – leukemi, myeloid
- MeSH C15.378.190.636 – myeloproliferativa störningar
- MeSH C15.378.190.636.085 – anemi, myeloftisk
- MeSH C15.378.190.636.276 – leukemi, erytroblastisk, akut
- MeSH C15.378.190.636.484 – leukemoid reaktion
- MeSH C15.378.190.636.581 – myelofibros
- MeSH C15.378.190.636.636 – myeloid metaplasi
- MeSH C15.378.190.636.753 – polycytemia vera
- MeSH C15.378.190.636.860 – trombocytos
- MeSH C15.378.190.636.860.800 – trombocytemi, hemorragisk
MeSH C15.378.400 – hematologiska neoplasmer
MeSH C15.378.420 – hemoglobinopatier
- MeSH C15.378.420.155 – anemi, sicklecell
- MeSH C15.378.420.155.440 – hemoglobin sc sjukdom
- MeSH C15.378.420.155.668 – sicklecellsdrag
- MeSH C15.378.420.463 – hemoglobin c-sjukdom
- MeSH C15.378.420.826 – talassemi
- MeSH C15.378.420.826.100 – alfa-talassemi
- MeSH C15.378.420.826.100.350 – hydrops fetalis
- MeSH C15.378.420.826.150 – beta-talassemi
MeSH C15.378.463 – hemorragiska störningar
- MeSH C15.378.463.067 – afibrinogenemi
- MeSH C15.378.463.080 – bernard-souliers syndrom
- MeSH C15.378.463.250 – disseminerad intravaskulär koagulation
- MeSH C15.378.463.300 – faktor v brist
- MeSH C15.378.463.310 – faktor vii-brist
- MeSH C15.378.463.320 – faktor x brist
- MeSH C15.378.463.325 – faktor xi-brist
- MeSH C15.378.463.330 – faktor xii-brist
- MeSH C15.378.463.335 – faktor xiii brist
- MeSH C15.378.463.500 – hemofili a
- MeSH C15.378.463.510 – hemofili b
- MeSH C15.378.463.550 – hypoprotrombinemier
- MeSH C15.378.463.735 – brist på trombocytlagringspool
- MeSH C15.378.463.735.400 – hermanski-pudlak syndrom
- MeSH C15.378.463.740 – purpura, trombocytopenisk, idiopatisk
- MeSH C15.378.463.810 – trombasteni
- MeSH C15.378.463.825 – trombocytemi, hemorragisk
- MeSH C15.378.463.835 – vaskulära hemostatiska störningar
- MeSH C15.378.463.835.140 – kryoglobulinemi
- MeSH C15.378.463.835.240 – ehlers-danlos syndrom
- MeSH C15.378.463.835.385 – hemangiom, kavernös
- MeSH C15.378.463.835.385.500 – hemangiom, kavernös, centrala nervsystemet
- MeSH C15.378.463.835.460 – multipelt myelom
- MeSH C15.378.463.835.530 – pseudoxanthoma elasticum
- MeSH C15.378.463.835.550 – purpura, hyperglobulinemisk
- MeSH C15.378.463.835.580 – purpura, schoenlein-henoch
- MeSH C15.378.463.835.800 – skörbjugg
- MeSH C15.378.463.835.810 – shwartzman-fenomen
- MeSH C15.378.463.835.900 – telangiektasi, ärftlig hemorragisk
- MeSH C15.378.463.835.960 – waldenström makroglobulinemi
- MeSH C15.378.463.841 – K-vitaminbrist
- MeSH C15.378.463.841.464 – hemorragisk sjukdom hos nyfödda
- MeSH C15.378.463.920 – von willebrands sjukdom
- MeSH C15.378.463.950 – waterhouse-friderichsens syndrom
- MeSH C15.378.463.960 – wiskott-aldrichs syndrom
MeSH C15.378.553 – leukocytrubbningar
- MeSH C15.378.553.231 – eosinofili
- MeSH C15.378.553.231.085 – angiolymphoid hyperplasi med eosinofili
- MeSH C15.378.553.231.335 – eosinofili-myalgisyndrom
- MeSH C15.378.553.231.348 – eosinofilt granulom
- MeSH C15.378.553.231.549 – hypereosinofilt syndrom
- MeSH C15.378.553.231.549.750 – pulmonell eosinofili
- MeSH C15.378.553.381 – infektiös mononukleos
- MeSH C15.378.553.475 – leukocytos
- MeSH C15.378.553.475.428 – leukemoid reaktion
- MeSH C15.378.553.475.604 – lymfocytos
- MeSH C15.378.553.546 – leukopeni
- MeSH C15.378.553.546.184 – agranulocytos
- MeSH C15.378.553.546.184.564 – neutropeni
- MeSH C15.378.553.546.605 – lymfopeni
- MeSH C15.378.553.546.605.800 – t-lymfocytopeni, idiopatisk cd4-positiv
- MeSH C15.378.553.560 – leukostas
- MeSH C15.378.553.696 – pelger-huet anomali
- MeSH C15.378.553.774 – baktericid dysfunktion av fagocyter
- MeSH C15.378.553.774.257 – chediak-higashi syndrom
- MeSH C15.378.553.774.535 – granulomatös sjukdom, kronisk
- MeSH C15.378.553.774.600 – jobbsyndrom
MeSH C15.378.619 – methemoglobinemi
MeSH C15.378.700 – pancytopeni
MeSH C15.378.738 – polycytemi
MeSH C15.378.785 – graviditetskomplikationer, hematologiska
MeSH C15.378.800 – preleukemi
MeSH C15.378.896 – sulfhemoglobinemi
MeSH C15.378.925 – trombofili
- MeSH C15.378.925.050 – aktiverat protein c-resistens
- MeSH C15.378.925.075 – antitrombin iii-brist
- MeSH C15.378.925.220 – disseminerad intravaskulär koagulation
- MeSH C15.378.925.795 – protein c-brist
- MeSH C15.378.925.800 – proteinbrist
- MeSH C15.378.925.850 – purpura, trombotisk trombocytopenisk
MeSH C15.604 – lymfatiska sjukdomar
MeSH C15.604.315 – lymfadenit
- MeSH C15.604.315.249 – kattskrapssjukdom
- MeSH C15.604.315.300 – histiocytisk nekrotiserande lymfadenit
- MeSH C15.604.315.618 – mesenterisk lymfadenit
- MeSH C15.604.315.809 – tuberkulos, lymfkörtel
MeSH C15.604.360 – lymfangiektas
- MeSH C15.604.360.500 – lymfangiektas, tarm
MeSH C15.604.406 – lymfangit
MeSH C15.604.451 – lymfatiska abnormiteter
- MeSH C15.604.451.500 – lymfangiektas, tarm
MeSH C15.604.496 – lymfödem
MeSH C15.604.510 – lymfocele
MeSH C15.604.515 – lymfoproliferativa störningar
- MeSH C15.604.515.032 – agammaglobulinemi
- MeSH C15.604.515.245 – jättelymfkörtelhyperplasi
- MeSH C15.604.515.292 – granulom
- MeSH C15.604.515.292.007 – angiolymphoid hyperplasi med eosinofili
- MeSH C15.604.515.292.015 – Churg–Strauss syndrom
- MeSH C15.604.515.435 – tungkedjesjukdom
- MeSH C15.604.515.435.512 – immunproliferativ tunntarmssjukdom
- MeSH C15.604.515.509 – immunoblastisk lymfadenopati
- MeSH C15.604.515.516 – infektiös mononukleos
- MeSH C15.604.515.553 – leukemi, hårcell
- MeSH C15.604.515.560 – leukemi, lymfocytisk
- MeSH C15.604.515.561 – leukemi, myeloid
- MeSH C15.604.515.561.550 – leukemi, icke-lymfocytisk, akut
- MeSH C15.604.515.561.550.512 – leukemi, myelocytisk, akut
- MeSH C15.604.515.562 – lymfangiomyom
- MeSH C15.604.515.562.465 – lymfangioleiomyomatos
- MeSH C15.604.515.569 – lymfom
- MeSH C15.604.515.569.355 – Hodgkins sjukdom
- MeSH C15.604.515.569.480 – lymfom, icke-hodgkin
- MeSH C15.604.515.569.480.150 – lymfom, b-cell
- MeSH C15.604.515.569.480.150.165 – burkitt lymfom
- MeSH C15.604.515.569.480.150.450 – lymfom, aids-relaterat
- MeSH C15.604.515.569.480.150.570 – lymfom, slemhinneassocierad lymfoid vävnad
- MeSH C15.604.515.569.480.150.700 – lymfom, småcelligt
- MeSH C15.604.515.569.480.300 – lymfom, diffust
- MeSH C15.604.515.569.480.300.300 – lymfom, storcellig, diffus
- MeSH C15.604.515.569.480.300.450 – lymfom, storcelligt, immunoblastiskt
- MeSH C15.604.515.569.480.300.475 – lymfom, lymfoblastiskt
- MeSH C15.604.515.569.480.300.500 – lymfom, blandad cell, diffus
- MeSH C15.604.515.569.480.300.725 – lymfom, små kluvna celler, diffust
- MeSH C15.604.515.569.480.300.725.500 – lymfom, mantelcell
- MeSH C15.604.515.569.480.300.750 – lymfom, små lymfocyter
- MeSH C15.604.515.569.480.300.775 – lymfom, liten icke-klyvd cell
- MeSH C15.604.515.569.480.350 – lymfom, follikulärt
- MeSH C15.604.515.569.480.350.350 – lymfom, storcelligt, follikulärt
- MeSH C15.604.515.569.480.350.525 – lymfom, blandcell, follikulärt
- MeSH C15.604.515.569.480.350.750 – lymfom, små kluvna celler, follikulärt
- MeSH C15.604.515.569.480.425 – lymfom, höggradigt
- MeSH C15.604.515.569.480.425.450 – lymfom, storcelligt, immunoblastiskt
- MeSH C15.604.515.569.480.425.475 – lymfom, lymfoblastiskt
- MeSH C15.604.515.569.480.425.775 – lymfom, liten icke-klyvd cell
- MeSH C15.604.515.569.480.425.775.165 – burkitt lymfom
- MeSH C15.604.515.569.480.450 – lymfom, medelgradig
- MeSH C15.604.515.569.480.450.300 – lymfom, storcelligt, diffust
- MeSH C15.604.515.569.480.450.350 – lymfom, storcelligt, follikulärt
- MeSH C15.604.515.569.480.450.500 – lymfom, blandad cell, diffus
- MeSH C15.604.515.569.480.450.725 – lymfom, små kluvna celler, diffust
- MeSH C15.604.515.569.480.450.725.500 – lymfom, mantelcell
- MeSH C15.604.515.569.480.475 – lymfom, storcelligt
- MeSH C15.604.515.569.480.475.300 – lymfom, storcelligt, diffust
- MeSH C15.604.515.569.480.475.350 – lymfom, storcelligt, follikulärt
- MeSH C15.604.515.569.480.475.450 – lymfom, storcelligt, immunoblastiskt
- MeSH C15.604.515.569.480.475.465 – lymfom, storcelligt, ki-1
- MeSH C15.604.515.569.480.475.475 – lymfom, lymfoblastiskt
- MeSH C15.604.515.569.480.500 – lymfom, låggradigt
- MeSH C15.604.515.569.480.500.525 – lymfom, blandcell, follikulärt
- MeSH C15.604.515.569.480.500.570 – lymfom, slemhinneassocierad lymfoid vävnad
- MeSH C15.604.515.569.480.500.750 – lymfom, små kluvna celler, follikulärt
- MeSH C15.604.515.569.480.500.770 – lymfom, små lymfocyter
- MeSH C15.604.515.569.480.550 – lymfom, blandad cell
- MeSH C15.604.515.569.480.550.500 – lymfom, blandad cell, diffus
- MeSH C15.604.515.569.480.550.525 – lymfom, blandcell, follikulärt
- MeSH C15.604.515.569.480.700 – lymfom, småcelligt
- MeSH C15.604.515.569.480.700.725 – lymfom, små kluvna celler, diffust
- MeSH C15.604.515.569.480.700.725.500 – lymfom, mantelcell
- MeSH C15.604.515.569.480.700.730 – lymfom, små kluvna celler, follikulärt
- MeSH C15.604.515.569.480.700.750 – lymfom, små lymfocyter
- MeSH C15.604.515.569.480.700.775 – lymfom, liten icke-klyvd cell
- MeSH C15.604.515.569.480.750 – lymfom, t-cell
- MeSH C15.604.515.569.480.750.475 – lymfom, lymfoblastiskt
- MeSH C15.604.515.569.480.750.800 – lymfom, t-cell, kutan
- MeSH C15.604.515.569.480.750.800.465 – lymfom, storcelligt, ki-1
- MeSH C15.604.515.569.480.750.800.550 – mycosis fungoides
- MeSH C15.604.515.569.480.750.800.775 – sezary syndrom
- MeSH C15.604.515.569.480.750.825 – lymfom, t-cell, perifert
- MeSH C15.604.515.569.480.875 – lymfom, odifferentierat
- MeSH C15.604.515.569.480.875.300 – lymfom, storcelligt, diffust
- MeSH C15.604.515.569.480.875.775 – lymfom, små icke kluvna celler
- MeSH C15.604.515.569.480.875.775.165 – burkitt lymfom
- MeSH C15.604.515.571 – lymfomatoid granulomatosis
- MeSH C15.604.515.700 – mareks sjukdom
- MeSH C15.604.515.827 – sarkoidos
- MeSH C15.604.515.827.725 – sarkoidos, lung
- MeSH C15.604.515.827.865 – uveoparotidfeber
- MeSH C15.604.515.841 – sezary syndrom
- MeSH C15.604.515.880 – tumörlyssyndrom
- MeSH C15.604.515.925 – waldenström makroglobulinemi
MeSH C15.604.560 – mukokutant lymfkörtelsyndrom
MeSH C15.604.613 – pseudolymfom
MeSH C15.604.667 – retikuloendotelios
- MeSH C15.604.667.358 – Gauchers sjukdom
- MeSH C15.604.667.400 – histiocytos
- MeSH C15.604.667.400.390 – histiocytiska störningar, maligna
- MeSH C15.604.667.400.390.400 – histiocytos, malign
- MeSH C15.604.667.400.390.500 – leukemi, monocytisk, akut
- MeSH C15.604.667.400.390.550 – lymfom, storcelligt
- MeSH C15.604.667.400.390.550.465 – lymfom, storcelligt, ki-1
- MeSH C15.604.667.400.400 – histiocytos, langerhans-cell
- MeSH C15.604.667.400.400.360 – eosinofilt granulom
- MeSH C15.604.667.400.410 – histiocytos, icke-langerhans-cell
- MeSH C15.604.667.400.410.224 – Erdheim-chesters sjukdom
- MeSH C15.604.667.400.410.450 – histiocytos, sinus
- MeSH C15.604.667.400.410.575 – lymfohistiocytos, hemofagocytisk
- MeSH C15.604.667.400.410.625 – niemann-pick sjukdomar
- MeSH C15.604.667.400.410.800 – havsblått histiocytsyndrom
- MeSH C15.604.667.400.410.900 – xanthogranulom, juvenil
- MeSH C15.604.667.750 – mastcellssarkom
MeSH C15.604.744 – mjältsjukdomar
- MeSH C15.604.744.293 – hypersplenism
- MeSH C15.604.744.428 – myeloid metaplasi
- MeSH C15.604.744.617 – mjältinfarkt
- MeSH C15.604.744.680 – mjältneoplasmer
- MeSH C15.604.744.742 – mjältruptur
- MeSH C15.604.744.742.500 – splenos
- MeSH C15.604.744.909 – tuberkulos, mjälte
- MeSH C15.604.744.954 – vandrande mjälte
MeSH C15.604.816 – tymushyperplasi
MeSH C15.604.861 – tymus neoplasmer
MeSH C15.604.921 – tuberkulos, lymfkörtel
Listan fortsätter vid Lista över MeSH-koder (C16) .
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