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KrankheitsverzeichnisSyndrome
Krankheitsverzeichnis · Modifikatoren und Verweise
Modifikatoren und Verweise · icd10cm-index-April-1-2026-XML.xml
Syndromehypoglycemic(familial) (neonatal)
E16.2
Syndromehypokalemic
E87.6
Syndromehyponatremic
E87.1
Syndromehypopituitarism
E23.0
Syndromehypoplastic left-heart
Q23.4
Syndromehypopotassemia
E87.6
Syndromehyposmolality
E87.1
Syndromehypotension, maternal
O26.5-
Syndromehypothenar hammer
I73.89
Syndromehypoventilation, obesity(OHS)
E66.2
SyndromeICF(intravascular coagulation-fibrinolysis)
D65
Syndromeidiopathic
Syndrome › idiopathiccardiorespiratory distress, newborn
P22.0
Syndrome › idiopathicnephrotic(infantile)
N04.9
Syndromeiliotibial band
M76.3-
Syndromeimmobility, immobilization(paraplegic)
M62.3
Syndromeimmune effector cell-associated neurotoxicity(ICANS)
G92.00
Syndrome › immune effector cell-associated neurotoxicity(ICANS)grade
Syndrome › immune effector cell-associated neurotoxicity(ICANS) › grade1
G92.01
Syndrome › immune effector cell-associated neurotoxicity(ICANS) › grade2
G92.02
Syndrome › immune effector cell-associated neurotoxicity(ICANS) › grade3
G92.03
Syndrome › immune effector cell-associated neurotoxicity(ICANS) › grade4
G92.04
Syndrome › immune effector cell-associated neurotoxicity(ICANS) › grade5
G92.05
Syndrome › immune effector cell-associated neurotoxicity(ICANS) › gradeunspecified
G92.00
Syndromeimmune reconstitution
D89.3
Syndromeimmune reconstitution inflammatory [IRIS]
D89.3
Syndromeimmunity deficiency, combined
D81.9
Syndromeimmunodeficiency
Syndrome › immunodeficiencyacquired
See: Human, immunodeficiency virus (HIV) disease
Syndrome › immunodeficiencycombined
D81.9
Syndromeimpending coronary
I20.0
Syndromeimpingement, shoulder
M75.4-
Syndromeinappropriate secretion of antidiuretic hormone
E22.2
Syndromeinfant
Syndrome › infantof diabetic mother
P70.1
Syndrome › infantgestational diabetes
P70.0
Syndromeinfantilism(pituitary)
E23.0
Syndromeinferior vena cava
I87.1
Syndromeinspissated bile(newborn)
P59.1
Syndromeinstitutional(childhood)
F94.2
Syndromeinsufficient sleep
F51.12
Syndromeinsulin resistance
Syndrome › insulin resistancetype A
E88.811
Syndrome › insulin resistancetype B
E88.818
Syndromeintermediate coronary(artery)
I20.0
Syndromeinterspinous ligament
See: Spondylopathy, specified NEC
Syndromeintestinal
Syndrome › intestinalcarcinoid
E34.09
Syndrome › intestinalknot
K56.2
Syndromeintravascular coagulation-fibrinolysis(ICF)
D65
Syndromeiodine-deficiency, congenital
E00.9
Syndrome › iodine-deficiency, congenitaltype
Syndrome › iodine-deficiency, congenital › typemixed
E00.2
Syndrome › iodine-deficiency, congenital › typemyxedematous
E00.1
Syndrome › iodine-deficiency, congenital › typeneurological
E00.0
SyndromeIRDS(idiopathic respiratory distress, newborn)
P22.0
Syndromeirritable
Syndrome › irritablebowel
K58.9
Syndrome › irritable › bowelwith
Syndrome › irritable › bowel › withconstipation
K58.1
Syndrome › irritable › bowel › withdiarrhea
K58.0
Syndrome › irritable › bowelmixed
K58.2
Syndrome › irritable › bowelpsychogenic
F45.8
Syndrome › irritable › bowelspecified NEC
K58.8
Syndrome › irritableheart(psychogenic)
F45.8
Syndrome › irritableweakness
F48.8
Syndromeischemic
Syndrome › ischemicbowel(transient)
K55.9
Syndrome › ischemic › bowel(transient)chronic
K55.1
Syndrome › ischemic › bowel(transient)due to mesenteric artery insufficiency
K55.1
Syndrome › ischemicsteal
T82.898
SyndromeIVC(intravascular coagulopathy)
D65
SyndromeIvemark's
Q89.01
SyndromeJaccoud's
See: Arthropathy, postrheumatic, chronic
SyndromeJackson's
G83.89
SyndromeJakob-Creutzfeldt
See: Creutzfeldt-Jakob disease or syndrome
Syndromejaw-winking
Q07.8
SyndromeJervell-Lange-Nielsen
I45.81
Syndromejet lag
G47.25
SyndromeJob's
D71.8
SyndromeJoseph-Diamond-Blackfan
D61.01
Syndromejugular foramen
G52.7
SyndromeKabuki(type 1, due to KMT2D mutation) (type 2, due to KDM6A mutation)
Q89.81
SyndromeKanner's(autism)
F84.0
SyndromeKartagener's
Q89.3
SyndromeKelly's
D50.1
SyndromeKimmelstiel-Wilson
See: Diabetes, specified type, with Kimmelstiel-Wilson disease
SyndromeKleefstra
Q87.86
SyndromeKlein(e)-Levine
G47.13
SyndromeKlippel-Feil(brevicollis)
Q76.1
SyndromeKöhler-Pellegrini-Stieda
See: Bursitis, tibial collateral
SyndromeKönig's
K59.89
SyndromeKorsakoff(-Wernicke) (nonalcoholic)
F04
Syndrome › Korsakoff(-Wernicke) (nonalcoholic)alcoholic
F10.26
SyndromeKostmann's
D70.0
SyndromeKrabbe's congenital muscle hypoplasia
Q79.8
Syndromelabyrinthine
Subcategory: H83.2
Syndromelacunar NEC
G46.7
SyndromeLambert-Eaton
G70.80
Syndrome › Lambert-Eatonin
Syndrome › Lambert-Eaton › inneoplastic disease
G73.1
Syndrome › Lambert-Eaton › inspecified disease NEC
G70.81
SyndromeLandau-Kleffner
See: Epilepsy, specified NEC
SyndromeLarsen's
Q74.8
SyndromeLassueur Graham-Little Piccardi
L66.19
Syndromelateral
Syndrome › lateralcutaneous nerve of thigh
G57.1-
Syndrome › lateralmedullary
G46.4
SyndromeLaunois'
E22.0
SyndromeLaurence-Moon
Q87.84
SyndromeLawrence
E88.12
Syndromelazy
Syndrome › lazyleukocyte
D70.8
Syndrome › lazyposture
M62.3
SyndromeLemierre
I80.8
SyndromeLennox-Gastaut
G40.812
Syndrome › Lennox-Gastautintractable
G40.814
Syndrome › Lennox-Gastaut › intractablewith status epilepticus
G40.813
Syndrome › Lennox-Gastaut › intractablewithout status epilepticus
G40.814
Syndrome › Lennox-Gastautnot intractable
G40.812
Syndrome › Lennox-Gastaut › not intractablewith status epilepticus
G40.811
Syndrome › Lennox-Gastaut › not intractablewithout status epilepticus
G40.812
Syndromelenticular, progressive
E83.01
SyndromeLeopold-Levi's
E05.90
SyndromeLev's
I44.2
SyndromeLi-Fraumeni
Z15.01
SyndromeLichtheim's
D51.0
SyndromeLightwood's
N25.89
SyndromeLignac(de Toni) (-Fanconi) (-Debré)
E72.09
Syndrome › Lignac(de Toni) (-Fanconi) (-Debré)with cystinosis
E72.04
SyndromeLikoff's
I20.89
Syndromelimbic epilepsy personality
F07.0
Syndromeliver-kidney
K76.7
Syndromelobotomy
F07.0
SyndromeLöffler's
J82.89
Syndromelong arm 18 or 21 deletion
Q93.89
Syndromelong QT
I45.81
SyndromeLouis-Barré
G11.3
Syndromelow
Syndrome › lowatmospheric pressure
T70.29
Syndrome › lowback
M54.50
Syndrome › lowoutput(cardiac)
I50.9
Syndromelower radicular, newborn(birth injury)
P14.8
SyndromeLuetscher's(dehydration)
E86.0
SyndromeLupus anticoagulant
D68.62
SyndromeLutembacher's
Q21.19
Syndromemacrophage activation
D76.1
Syndrome › macrophage activationdue to infection
D76.2
Syndromemagnesium-deficiency
R29.0
SyndromeMajeed
M04.8
SyndromeMal de Debarquement
R42
Syndromemalabsorption
K90.9
Syndrome › malabsorptionpostsurgical
K91.2
Syndromemalformation, congenital, due to
Syndrome › malformation, congenital, due toalcohol
Q86.0
Syndrome › malformation, congenital, due toexogenous cause NEC
Q86.8
Syndrome › malformation, congenital, due tohydantoin
Q86.1
Syndrome › malformation, congenital, due towarfarin
Q86.2
Syndromemalignant
Syndrome › malignantcarcinoid
E34.00
Syndrome › malignantneuroleptic
G21.0
SyndromeMallory-Weiss
K22.6
Syndromemandibulofacial dysostosis
Q75.4
Syndromemanic-depressive
See: Disorder, bipolar
Syndromemaple-syrup-urine
E71.0
SyndromeMarable's
I77.4
SyndromeMarfan
Q87.40
Syndrome › Marfanwith
Syndrome › Marfan › withcardiovascular manifestations
Q87.418
Syndrome › Marfan › with › cardiovascular manifestationsaortic dilation
Q87.410
Syndrome › Marfan › withocular manifestations
Q87.42
Syndrome › Marfan › withskeletal manifestations
Q87.43
SyndromeMarie's(acromegaly)
E22.0
Syndromemast cell activation
See: Activation, mast cell
Syndromematernal hypotension
See: Syndrome, hypotension, maternal
SyndromeMay(-Hegglin)
D72.0
SyndromeMcArdle(-Schmidt) (-Pearson)
E74.04
SyndromeMcQuarrie's
E16.2
Syndromemeconium plug(newborn)
P76.0
SyndromeMED13L(mediator complex subunit 13L)
Q87.85
Syndromemedian arcuate ligament
I77.4
Syndromemediator complex subunit 13L(MED13L)
Q87.85
SyndromeMeekeren-Ehlers-Danlos
Q79.6
Syndromemegavitamin-B6
E67.2
SyndromeMeige
G24.4
SyndromeMELAS
E88.41
SyndromeMendelson's
O74.0
SyndromeMERRF(myoclonic epilepsy associated with ragged-red fibers)
E88.42
Syndromemesenteric
Syndrome › mesentericartery(superior)
K55.1
Syndrome › mesentericvascular insufficiency
K55.1
Syndromemetabolic
E88.810
Syndromemetastatic carcinoid
E34.00
Syndromemicrognathia-glossoptosis
Q87.0
Syndromemidbrain NEC
G93.89
Syndromemiddle lobe(lung)
J98.19
Syndromemiddle radicular
G54.0
Syndromemigraine
G43.909-
See also: Migraine
SyndromeMikulicz'
K11.8
Syndromemilk-alkali
E83.52