Index to Diseases and Injuries: M
604 entries
- Macacus earQ17.3
- Maceration, wet feet, tropical (syndrome)T69.02-
- MacLeod's syndromeJ43.0
- Macrocephalia, macrocephalyQ75.3
- Macrocheilia, macrochilia (congenital)Q18.6
- MacrocolonQ43.1
- MacrocorneaQ15.8
- Macrocytic
- MacrocytosisD75.89
- Macrodactylia, macrodactylism (fingers) (thumbs)Q74.0
- MacrodontiaK00.2
- MacrogeniaM26.05
- Macrogenitosomia (adrenal) (male) (praecox)E25.9
- Macroglobulinemia (idiopathic) (primary)C88.0-
- Macroglossia (congenital)Q38.2
- Macrognathia, macrognathism (congenital) (mandibular) (maxillary)M26.09
- Macrogyria (congenital)Q04.8
- Macrohydrocephalus
- Macromastia
- MacrophthalmosQ11.3
- MacropsiaH53.15
- MacrosigmoidK59.39
- Macrospondylitis , acromegalicE22.0
- Macrostomia (congenital)Q18.4
- Macrotia (external ear) (congenital)Q17.1
- Macula
- Maculae ceruleaeB85.1
- Maculopathy, toxic
- Madarosis (eyelid)H02.729
- Madelung's
- Madness
- Madura
- MaduromycosisB47.0
- Maffucci's syndromeQ78.4
- Magnesium metabolism disorder
- Main en griffe (acquired)
- Maintenance (encounter for)
- Majocchi's
- Major
- Malabar itch (any site)B35.5
- MalabsorptionK90.9
- Malacia, bone (adult)M83.9
- Malacoplakia
- Malacosteon, juvenile
- Maladaptation
- Maladie de RogerQ21.0
- Maladjustment
- MalaiseR53.81
- Malakoplakia
- Malaria, malarial (fever)B54
- MalassimilationK90.9
- Malassez's disease (cystic)N50.89
- Mal de los pintos
- Mal de merT75.3
- Maldescent, testisQ53.9
- Maldevelopment
- Male type pelvisQ74.2
- Malformation (congenital)
- Malfunction
- Malherbe's tumor
- Malibu diseaseL98.8
- Malignancy
- Malignant
- Malingerer, malingeringZ76.5
- Mallet finger (acquired)
- MalleusA24.0
- Mallory's bodiesR89.7
- Mallory-Weiss syndromeK22.6
- MalnutritionE46
- Malocclusion (teeth)M26.4
- Malposition
- MalpostureR29.3
- Malrotation
- Maltreatment
- Malta fever
- Maltworker's lungJ67.4
- Malunion, fracture
- MammillitisN61.0
- Mammitis
- Mammogram (examination)Z12.39
- MammoplasiaN62
- Management (of)
- Mangled
- Mania (monopolar)
- Manic depressionF31.9
- Manic-depressive insanity, psychosis, or syndrome
- MannosidosisE77.1
- Mansonelliasis, mansonellosisB74.4
- Manson's
- Manual
- Maple-bark-stripper's lung (disease)J67.6
- Maple-syrup-urine diseaseE71.0
- Marable's syndrome (celiac artery compression)I77.4
- MarasmusE41
- Marble
- Marburg virus diseaseA98.3
- March
- Marchesani (-Weill) syndromeQ87.0
- Marchiafava (-Bignami) syndrome or diseaseG37.1
- Marchiafava-Micheli syndromeD59.5
- Marcus Gunn's syndromeQ07.8
- Marfan syndrome
- Marie-Bamberger disease
- Marie-Charcot-Tooth neuropathic muscular atrophyG60.0
- Marie's
- Marie-Strümpell arthritis, disease or spondylitis
- Marion's disease (bladder neck obstruction)N32.0
- Marital conflictZ63.0
- Mark
- Marker heterochromatin
- Maroteaux-Lamy syndrome (mild) (severe)E76.29
- Marrow (bone)
- Marseilles feverA77.1
- Marsh fever
- Marshall's (hidrotic) ectodermal dysplasiaQ82.4
- Marsh's disease (exophthalmic goiter)E05.00
- Masculinization (female) with adrenal hyperplasiaE25.9
- MasculinovoblastomaD27.-
- Masochism (sexual)F65.51
- Mason's lungJ62.8
- Mass
- Massive
- Mast cell
- MastalgiaN64.4
- Masters-Allen syndromeN83.8
- Mastitis (acute) (diffuse) (nonpuerperal) (subacute)N61.0
- Mastocytoma (extracutaneous)D47.09
- MastocytosisD47.09
- MastodyniaN64.4
- Mastoid
- MastoidalgiaH92.0
- Mastoiditis (coalescent) (hemorrhagic) (suppurative)H70.9-
- Mastopathy, mastopathiaN64.9
- Mastoplasia, mastoplastiaN62
- Masturbation (excessive)F98.8
- Maternal care (for)
- Matheiu's disease (leptospiral jaundice)A27.0
- Mauclaire's disease or osteochondrosis
- Maxcy's diseaseA75.2
- Maxilla, maxillary
- May (-Hegglin) anomaly or syndromeD72.0
- McArdle (-Schmid)(-Pearson) disease (glycogen storage)E74.04
- McCune-Albright syndromeQ78.1
- McQuarrie's syndrome (idiopathic familial hypoglycemia)E16.2
- Meadow's syndromeQ86.1
- Measles (black) (hemorrhagic) (suppressed)B05.9
- Meatitis, urethral
- Meatus, meatal
- Meat-wrappers' asthmaJ68.9
- ME/CFS (myalgic encephalomyelitis/chronic fatigue syndrome)G93.32
- Meckel-Gruber syndromeQ61.9
- Meckel's diverticulitis, diverticulum (displaced) (hypertrophic)Q43.0
- Meconium
- MED13L (mediator complex subunit 13L) syndromeQ87.85
- Median
- Mediastinal shiftR93.89
- Mediastinitis (acute) (chronic)J98.51
- Mediastinopericarditis
- Mediastinum, mediastinal
- Mediator complex subunit 13L (MED13L) syndromeQ87.85
- Medicine poisoning
- Mediterranean
- Medulla
- Medullary cystic kidneyQ61.5
- Medullated fibers
- Medulloblastoma
- Medulloepithelioma
- Medullomyoblastoma
- Meekeren-Ehlers-Danlos syndromeQ79.69
- Megacolon (acquired) (functional) (not Hirschsprung's disease) (in)K59.39
- Megaesophagus (functional)K22.0
- MegalencephalyQ04.5
- Megalerythema (epidemic)B08.3
- MegaloappendixQ43.8
- Megalocephalus, megalocephaly NECQ75.3
- MegalocorneaQ15.8
- Megalocytic anemiaD53.1
- Megalodactylia (fingers) (thumbs) (congenital)Q74.0
- MegaloduodenumQ43.8
- Megaloesophagus (functional)K22.0
- Megalogastria (acquired)K31.89
- MegalophthalmosQ11.3
- MegalopsiaH53.15
- Megalosplenia
- MegaloureterN28.82
- MegarectumK62.89
- MegasigmoidK59.39
- MegaureterN28.82
- Megavitamin-B6 syndromeE67.2
- Megrim
- Meibomian
- Meibomitis
- Meige-Milroy disease (chronic hereditary edema)Q82.0
- Meige's syndromeQ82.0
- Melalgia, nutritionalE53.8
- MelancholiaF32.A
- MelanemiaR79.89
- Melanoameloblastoma
- Melanoblastoma
- Melanocarcinoma
- Melanocytoma, eyeballD31.9-
- Melanocytosis, neurocutaneousQ82.8
- Melanoderma, melanodermiaL81.4
- Melanodontia, infantileK03.89
- MelanodontoclasiaK03.89
- Melanoepithelioma
- Melanoma (malignant)C43.9
- Melanosarcoma
- MelanosisL81.4
- MelanuriaR82.998
- MELAS syndromeE88.41
- MelasmaL81.1
- MelenaK92.1
- Meleney's
- MelioidosisA24.9
- Melitensis, febrisA23.0
- Melkersson (-Rosenthal) syndromeG51.2
- Mellitus, diabetes
- Melorheostosis (bone)
- MeloschisisQ18.4
- MelotiaQ17.4
- Membrana
- Membranacea placentaO43.19-
- Membranaceous uterusN85.8
- Membrane (s) , membranous
- Membranitis
- Memory disturbance, lack or loss
- Menadione deficiencyE56.1
- Menarche
- Mendacity, pathologicF60.2
- Mendelson's syndrome (due to anesthesia)J95.4
- Ménétrier's disease or syndromeK29.60
- Ménière's disease, syndrome or vertigoH81.0-
- Meninges, meningeal
- Meningioma
- Meningiomatosis (diffuse)
- Meningism
- Meningismus (infectional) (pneumococcal)R29.1
- Meningitis (basal) (basic) (brain) (cerebral) (cervical) (congestive) (diffuse) (hemorrhagic) (infantile) (membranous) (metastatic) (nonspecific) (pontine) (progressive) (simple) (spinal) (subacute) (sympathetic) (toxic)G03.9
- Meningocele (spinal)
- Meningocerebritis
- MeningococcemiaA39.4
- Meningococcus, meningococcalA39.9
- MeningoencephalitisG04.90
- Meningoencephalocele
- Meningoencephalomyelitis
- MeningoencephalomyelopathyG96.9
- MeningoencephalopathyG96.9
- Meningomyelitis
- Meningomyelocele
- Meningomyeloneuritis
- Meningoradiculitis
- Meningovascular
- Menkes' disease or syndromeE83.09
- MenometrorrhagiaN92.1
- Menopause, menopausal (asymptomatic) (state)Z78.0
- Menorrhagia (primary)N92.0
- MenostaxisN92.0
- Menses, retentionN94.89
- Menstrual
- Menstruation
- Mental
- Meralgia parestheticaG57.1-
- Mercurial
- MercurialismT56.1
- MERRF syndrome (myoclonic epilepsy associated with ragged-red fiber)E88.42
- Merkel cell tumor
- Merocele
- Meromelia
- Merzbacher-Pelizaeus diseaseE75.27
- Mesaortitis
- Mesarteritis
- Mesencephalitis
- Mesenchymoma
- Mesenteritis
- Mesentery, mesenteric
- Mesiodens, mesiodentesK00.1
- Mesio-occlusionM26.213
- Mesocolon
- Mesonephroma (malignant)
- Mesophlebitis
- Mesostromal dysgenesiaQ13.89
- Mesothelioma (malignant)C45.9
- Metabolic syndromeE88.810
- MetagonimiasisB66.8
- Metagonimus infestation (intestine)B66.8
- Metal
- MetamorphopsiaH53.15
- Metaplasia
- Metastasis, metastatic
- MetastrongyliasisB83.8
- MetatarsalgiaM77.4-
- Metatarsus, metatarsal
- Methadone use
- MethemoglobinemiaD74.9
- Methemoglobinuria
- MethioninemiaE72.19
- Methylmalonic acidemiaE71.120
- Metritis (catarrhal) (hemorrhagic) (septic) (suppurative)
- Metropathia hemorrhagicaN93.8
- Metroperitonitis
- MetrorrhagiaN92.1
- Metrorrhexis
- MetrosalpingitisN70.91
- MetrostaxisN93.8
- Metrovaginitis
- Meyer-Schwickerath and Weyers syndromeQ87.0
- Meynert's amentia (nonalcoholic)F04
- Mibelli's disease (porokeratosis)Q82.8
- Mice, joint
- Micrencephalon, micrencephalyQ02
- MicroalbuminuriaR80.9
- Microaneurysm, retinal
- Microangiopathy (peripheral)I73.9
- Microcalcifications, breastR92.0
- Microcephalus, microcephalic, microcephalyQ02
- MicrocheiliaQ18.7
- Microcolon (congenital)Q43.8
- Microcornea (congenital)Q13.4
- Microcytic
- Microdeletions NECQ93.88
- MicrodontiaK00.2
- MicrodrepanocytosisD57.40
- Microembolism
- MicroencephalonQ02
- Microfilaria streptocerca infestation
- Microgastria (congenital)Q40.2
- MicrogeniaM26.06
- Microgenitalia, congenital
- Microglioma
- Microglossia (congenital)Q38.3
- Micrognathia, micrognathism (congenital) (mandibular) (maxillary)M26.09
- Microgyria (congenital)Q04.3
- Microinfarct of heart
- Microlentia (congenital)Q12.8
- Microlithiasis, alveolar, pulmonaryJ84.02
- MicromastiaN64.82
- Micromyelia (congenital)Q06.8
- MicropenisQ55.62
- Microphakia (congenital)Q12.8
- Microphthalmos, microphthalmia (congenital)Q11.2
- MicropsiaH53.15
- Microscopic polyangiitis (polyarteritis)M31.7
- MicrosporidiosisB60.8
- Microsporon furfur infestationB36.0
- Microsporosis
- Microstomia (congenital)Q18.5
- Microtia (congenital) (external ear)Q17.2
- MicrotropiaH50.40
- Microvillus inclusion disease (MVD) (MVID)Q43.8
- Micturition
- Mid plane
- Middle
- Miescher's elastomaL87.2
- Mietens' syndromeQ87.2
- Migraine (idiopathic)G43.909
- Migrant, socialZ59.00
- Migration, anxiety concerningZ60.3
- Migratory, migrating
- Mikity-Wilson disease or syndromeP27.0
- Mikulicz' disease or syndromeK11.8
- MiliariaL74.3
- Miliary
- MiliumL72.0
- Milk
- Milk-alkali disease or syndromeE83.52
- Milk-leg (deep vessels) (nonpuerperal)
- Milkman's disease or syndromeM83.8
- Milky urine
- Millard-Gubler (-Foville) paralysis or syndromeG46.3
- Millar's asthmaJ38.5
- Miller Fisher syndromeG61.0
- Mills' disease
- Millstone maker's pneumoconiosisJ62.8
- Milroy's disease (chronic hereditary edema)Q82.0
- Minamata diseaseT56.1
- Miners' asthma or lungJ60
- Minkowski-Chauffard syndrome
- Minor
- Minor's disease (hematomyelia)G95.19
- Minot's disease (hemorrhagic disease) , newbornP53
- Minot-von Willebrand-Jurgens disease or syndrome (angiohemophilia)
- Minus (and plus) hand (intrinsic)
- Miosis (pupil)H57.03
- Mirizzi's syndrome (hepatic duct stenosis)K83.1
- Mirror writingF81.0
- MIS-AM35.81
- MIS-CM35.81
- Misadventure (of) (prophylactic) (therapeutic)T88.9
- MiscarriageO03.9
- Misdirection, aqueousH40.83-
- Misperception, sleep stateF51.02
- Misplaced, misplacement
- Missed
- Missing
- Misuse of drugsF19.99
- Mitchell's disease (erythromelalgia)I73.81
- Mite (s) (infestation)B88.9
- Mitral
- MittelschmerzN94.0
- Mixed
- MMN (multifocal motor neuropathy)G61.82
- MNGIE (Mitochondrial Neurogastrointestinal Encephalopathy) syndromeE88.49
- Mobile, mobility
- Mobitz heart block (atrioventricular)I44.1
- Moebius, Möbius
- Moeller's glossitisK14.0
- MOGAD (myelin oligodendrocyte glycoprotein antibody disease)G37.81
- Mohr's syndrome (Types I and II)Q87.0
- Mola destruensD39.2
- Molar pregnancyO02.0
- Molarization of premolarsK00.2
- Molding, head (during birth) - omit code
- Mole (pigmented)
- Molimen, molimina (menstrual)N94.3
- Molluscum contagiosum (epitheliale)B08.1
- Mönckeberg's arteriosclerosis, disease, or sclerosis
- Mondini's malformation (cochlea)Q16.5
- Mondor's diseaseI80.8
- Monge's diseaseT70.29
- Monilethrix (congenital)Q84.1
- MoniliasisB37.9
- Monitoring (encounter for)
- Monkey malariaB53.1
- MonkeypoxB04
- MonoarthritisM13.10
- Monoblastic
- Monochromat (ism), monochromatopsia (acquired) (congenital)H53.51
- Monocytic
- MonocytopeniaD72.818
- Monocytosis (symptomatic)D72.821
- Monomania
- MononeuritisG58.9
- MononeuropathyG58.9
- Mononucleosis, infectiousB27.90
- Monoparesis
- MonoplegiaG83.3-
- Monorchism, monorchidismQ55.0
- MonosomyQ93.9
- Monster, monstrosity (single)Q89.7
- Monteggia's fracture (-dislocation)S52.27-
- Mooren's ulcer (cornea)
- Moore's syndrome
- Mooser-Neill reactionA75.2
- Mooser's bodiesA75.2
- Morbidity not stated or unknownR69
- Morbilli
- Morbus
- Morel (-Stewart)(-Morgagni) syndromeM85.2
- Morel-Kraepelin disease
- Morel-Moore syndromeM85.2
- Morgagni's
- Morgagni-Stokes-Adams syndromeI45.9
- Morgagni-Stewart-Morel syndromeM85.2
- Morgagni-Turner (-Albright) syndromeQ96.9
- MoriaF07.0
- Moron (I.Q.50-69)F70
- MorpheaL94.0
- Morphinism (without remission)F11.20
- Morphinomania (without remission)F11.20
- Morquio (-Ullrich)(-Brailsford) disease or syndrome
- Mortification (dry) (moist)
- Morton's metatarsalgia (neuralgia)(neuroma) (syndrome)G57.6-
- Morvan's disease or syndromeG60.8
- Mosaicism, mosaic (autosomal) (chromosomal)
- Moschowitz' diseaseM31.19
- Mother yawA66.0
- Motion sickness (from travel, any vehicle) (from roundabouts or swings)T75.3
- Mottled, mottling, teeth (enamel) (endemic) (nonendemic)K00.3
- Mounier-Kuhn syndromeQ32.4
- Mountain
- Mouse, joint
- Mouth
- Movable
- Movements, dystonicR25.8
- Moyamoya diseaseI67.5
- MpoxB04
- MRSA (Methicillin resistant Staphylococcus aureus)
- MSD (multiple sulfatase deficiency)E75.26
- MSSA (Methicillin susceptible Staphylococcus aureus)
- Mucha-Habermann diseaseL41.0
- Mucinosis (cutaneous) (focal) (papular) (reticular erythematous) (skin)L98.5
- Mucocele
- Mucolipidosis
- MucopolysaccharidosisE76.3
- MucormycosisB46.5
- Mucositis (ulcerative)K12.30
- Mucositis necroticans agranulocytica
- Mucous
- MucoviscidosisE84.9
- Mucus
- MuguetB37.0
- Mulberry molars (congenital syphilis)A50.52
- Müllerian mixed tumor
- Multicystic kidney (development)Q61.4
- Multiparity (grand)Z64.1
- Multipartita placentaO43.19-
- Multiple, multiplex
- Multisystem inflammatory syndrome (in adult) (in children)M35.81
- MumpsB26.9
- MumuB74.9
- Münchhausen's syndrome
- Münchmeyer's syndrome
- Mural
- Murmur (cardiac) (heart) (organic)R01.1
- Murri's disease (intermittent hemoglobinuria)D59.6
- Muscle, muscular
- Musculoneuralgia
- Mushroom-workers' (pickers') disease or lungJ67.5
- Mushrooming hip
- Mutation (s)
- Mutism
- MVD (microvillus inclusion disease)Q43.8
- MVID (microvillus inclusion disease)Q43.8
- MyalgiaM79.10
- MyastheniaG70.9
- MyasthenicM62.81
- Mycelium infectionB49
- Mycetismus
- MycetomaB47.9
- Mycobacteriosis
- Mycobacterium, mycobacterial (infection)A31.9
- Mycoplasma (M.) pneumoniae, as cause of disease classified elsewhereB96.0
- Mycosis, mycoticB49
- Mydriasis (pupil)H57.04
- MyelateliaQ06.1
- Myelinolysis, pontine, centralG37.2
- Myelitis (acute) (ascending) (childhood) (chronic) (descending) (diffuse) (disseminated) (idiopathic) (pressure) (progressive) (spinal cord) (subacute)G04.91
- Myeloblastic
- Myeloblastoma
- Myelocele
- Myelocystocele
- Myelocytic
- MyelodysplasiaD46.9
- Myelodysplastic syndromeD46.9
- Myeloencephalitis
- MyelofibrosisD75.81
- Myelogenous
- Myeloid
- MyelokathexisD70.9
- MyeloleukodystrophyE75.29
- Myelolipoma
- Myeloma (multiple)C90.0-
- MyelomalaciaG95.89
- MyelomatosisC90.0-
- Myelomeningitis
- Myelomeningocele (spinal cord)
- Myelo-osteo-musculodysplasia hereditariaQ79.8
- Myelopathic
- Myelopathy (spinal cord)G95.9
- MyelophthisisD61.82
- MyeloradiculitisG04.91
- Myeloradiculodysplasia (spinal)Q06.1
- MyelosarcomaC92.3-
- MyelosclerosisD75.89
- Myelosis
- Myiasis (cavernous)B87.9
- Myoadenoma, prostate
- Myoblastoma
- Myocardial
- Myocardiopathy (congestive) (constrictive) (familial) (hypertrophic nonobstructive) (idiopathic) (infiltrative) (obstructive) (primary) (restrictive) (sporadic)I42.9
- Myocarditis (with arteriosclerosis)(chronic)(fibroid) (interstitial) (old) (progressive) (senile)I51.4
- Myocardium, myocardial
- Myocardosis
- Myoclonus, myoclonic, myoclonia (familial) (essential) (multifocal) (simplex)G25.3
- MyocytolysisI51.5
- Myodiastasis
- Myoendocarditis
- Myoepithelioma
- Myofasciitis (acute)
- Myofibroma
- MyofibromatosisD48.19
- MyofibrosisM62.89
- MyofibrositisM79.7
- Myoglobulinuria, myoglobinuria (primary)R82.1
- Myokymia, facialG51.4
- Myolipoma
- Myoma
- MyomalaciaM62.89
- Myometritis
- Myometrium
- Myonecrosis, clostridialA48.0
- MyopathyG72.9
- Myopericarditis
- Myopia (axial) (congenital)H52.1-
- Myosarcoma
- Myosis (pupil)H57.03
- MyositisM60.9
- Myospasia impulsivaF95.2
- Myotonia (acquisita) (intermittens)M62.89
- Myotonic pupil
- MyriapodiasisB88.2
- MyringitisH73.2-
- MysophobiaF40.228
- Mytilotoxism
- Myxadenitis labialisK13.0
- Myxedema (adult) (idiocy) (infantile) (juvenile)E03.9
- Myxochondrosarcoma
- Myxofibroma
- Myxofibrosarcoma
- MyxolipomaD17.9
- Myxoliposarcoma
- Myxoma
- Myxosarcoma
ICD-10-CM Index to Diseases and Injuries maintained by CDC/NCHS (public domain). Always confirm codes in the Tabular List.