ICD-10-CM Index to Diseases and Injuries — M
3,040 entries · page 6 of 8. An entry marked — has no code of its own; follow "see" to the listed term.
| Term | Code |
|---|---|
| Migraine (idiopathic), without aura, without mention of refractory migraine, with status migrainosus | G43.001 |
| Migraine (idiopathic), without aura, without mention of refractory migraine, without status migrainosus | G43.009 |
| Migraine (idiopathic), without refractory migraine | G43.909 |
| Migraine (idiopathic), without refractory migraine, with status migrainosus | G43.901 |
| Migraine (idiopathic), without refractory migraine, without status migrainosus | G43.909 |
| Migrant, social | Z59.00 |
| Migration, anxiety concerning | Z60.3 |
| Migratory, migrating — see also condition | — |
| Migratory, migrating, person | Z59.00 |
| Migratory, migrating, testis | Q55.29 |
| Mikity-Wilson disease or syndrome | P27.0 |
| Mikulicz' disease or syndrome | K11.8 |
| Miliaria | L74.3 |
| Miliaria, alba | L74.1 |
| Miliaria, apocrine | L75.2 |
| Miliaria, crystallina | L74.1 |
| Miliaria, profunda | L74.2 |
| Miliaria, rubra | L74.0 |
| Miliaria, tropicalis | L74.2 |
| Miliary — see condition | — |
| Milium | L72.0 |
| Milium, colloid | L57.8 |
| Milk-alkali disease or syndrome | E83.52 |
| Milk-leg (deep vessels) (nonpuerperal) — see Embolism, vein, lower extremity | — |
| Milk-leg (deep vessels) (nonpuerperal), complicating pregnancy | — |
| Milk-leg (deep vessels) (nonpuerperal), puerperal, postpartum, childbirth | O87.1 |
| Milk, crust | L21.0 |
| Milk, excessive secretion | O92.6 |
| Milk, poisoning — see Poisoning, food, noxious | — |
| Milk, retention | O92.79 |
| Milk, sickness — see Poisoning, food, noxious | — |
| Milk, spots | I31.0 |
| Milkman's disease or syndrome | M83.8 |
| Milky urine — see Chyluria | — |
| Millar's asthma | J38.5 |
| Millard-Gublerparalysis or syndrome (-Foville) | G46.3 |
| Miller Fisher syndrome | G61.0 |
| Mills' disease — see Hemiplegia | — |
| Millstone maker's pneumoconiosis | J62.8 |
| Milroy's disease (chronic hereditary edema) | Q82.0 |
| Minamata disease | T56.1 |
| Miners' asthma or lung | J60 |
| Minkowski-Chauffard syndrome — see Spherocytosis | — |
| Minor — see condition | — |
| Minor's disease (hematomyelia) | G95.19 |
| Minot-von Willebrand-Jurgens disease or syndrome (angiohemophilia) — see Disease, von Willebrand | — |
| Minot's disease, newborn (hemorrhagic disease) | P53 |
| Minus (and plus) hand (intrinsic) — see Deformity, limb, specified type NEC, forearm | — |
| Miosis (pupil) | H57.03 |
| Mirizzi's syndrome (hepatic duct stenosis) | K83.1 |
| Mirror writing | F81.0 |
| MIS-A | M35.81 |
| MIS-C | M35.81 |
| Misadventure (of) (prophylactic) (therapeutic) | T88.9 |
| Misadventure (of) (prophylactic) (therapeutic), infusion — see Complications, infusion | — |
| Misadventure (of) (prophylactic) (therapeutic), local applications (of fomentations, plasters, etc.) | T88.9 |
| Misadventure (of) (prophylactic) (therapeutic), local applications (of fomentations, plasters, etc.), burn or scald — see Burn | — |
| Misadventure (of) (prophylactic) (therapeutic), local applications (of fomentations, plasters, etc.), specified NEC | T88.8 |
| Misadventure (of) (prophylactic) (therapeutic), medical care (early) (late) | T88.9 |
| Misadventure (of) (prophylactic) (therapeutic), medical care (early) (late), adverse effect of drugs or chemicals — see Table of Drugs and Chemicals | — |
| Misadventure (of) (prophylactic) (therapeutic), medical care (early) (late), burn or scald — see Burn | — |
| Misadventure (of) (prophylactic) (therapeutic), medical care (early) (late), specified NEC | T88.8 |
| Misadventure (of) (prophylactic) (therapeutic), specified NEC | T88.8 |
| Misadventure (of) (prophylactic) (therapeutic), surgical procedure (early) (late) — see Complications, surgical procedure | — |
| Misadventure (of) (prophylactic) (therapeutic), transfusion — see Complications, transfusion | — |
| Misadventure (of) (prophylactic) (therapeutic), vaccination or other immunological procedure — see Complications, vaccination | — |
| Miscarriage | O03.9 |
| Misdirection, aqueous | — |
| Misperception, sleep state | F51.02 |
| Misplaced, misplacement, ear | Q17.4 |
| Misplaced, misplacement, kidney (acquired) | N28.89 |
| Misplaced, misplacement, kidney (acquired), congenital | Q63.2 |
| Misplaced, misplacement, organ or site, congenital NEC — see Malposition, congenital | — |
| Missed, abortion | O02.1 |
| Missed, delivery | O36.4 |
| Missing — see also Absence | — |
| Missing, string of intrauterine contraceptive device | T83.32 |
| Misuse of drugs | F19.99 |
| Mitchell's disease (erythromelalgia) | I73.81 |
| Mite (s) (infestation) | B88.9 |
| Mite (s) (infestation), diarrhea | B88.09 |
| Mite (s) (infestation), grain (itch) | B88.09 |
| Mite (s) (infestation), hair follicle (itch) | B88.09 |
| Mite (s) (infestation), in sputum | B88.09 |
| Mitral — see condition | — |
| Mittelschmerz | N94.0 |
| Mixed — see condition | — |
| MMN (multifocal motor neuropathy) | G61.82 |
| MNGIEsyndrome (Mitochondrial Neurogastrointestinal Encephalopathy) | E88.49 |
| Mobile, mobility, cecum | Q43.3 |
| Mobile, mobility, excessive — see Hypermobility | — |
| Mobile, mobility, gallbladder, congenital | Q44.1 |
| Mobile, mobility, kidney | N28.89 |
| Mobile, mobility, organ or site, congenital NEC — see Malposition, congenital | — |
| Mobitz heart block (atrioventricular) | I44.1 |
| Moebius, Möbius, disease (ophthalmoplegic migraine) — see Migraine, ophthalmoplegic | — |
| Moebius, Möbius, syndrome | Q87.0 |
| Moebius, Möbius, syndrome, congenital oculofacial paralysis (with other anomalies) | Q87.0 |
| Moebius, Möbius, syndrome, ophthalmoplegic migraine — see Migraine, ophthalmoplegic | — |
| Moeller's glossitis | K14.0 |
| MOGAD (myelin oligodendrocyte glycoprotein antibody disease) | G37.81 |
| Mohr's syndrome (Types I and II) | Q87.0 |
| Mola destruens | D39.2 |
| Molar pregnancy | O02.0 |
| Molarization of premolars | K00.2 |
| Mole (pigmented) — see also Nevus | — |
| Mole (pigmented), blood | O02.0 |
| Mole (pigmented), Breus' | O02.0 |
| Mole (pigmented), cancerous — see Melanoma | — |
| Mole (pigmented), carneous | O02.0 |
| Mole (pigmented), destructive | D39.2 |
| Mole (pigmented), fleshy | O02.0 |
| Mole (pigmented), hydatid, hydatidiform (benign) (complicating pregnancy) (delivered) (undelivered) | O01.9 |
| Mole (pigmented), hydatid, hydatidiform (benign) (complicating pregnancy) (delivered) (undelivered), classical | O01.0 |
| Mole (pigmented), hydatid, hydatidiform (benign) (complicating pregnancy) (delivered) (undelivered), complete | O01.0 |
| Mole (pigmented), hydatid, hydatidiform (benign) (complicating pregnancy) (delivered) (undelivered), incomplete | O01.1 |
| Mole (pigmented), hydatid, hydatidiform (benign) (complicating pregnancy) (delivered) (undelivered), invasive | D39.2 |
| Mole (pigmented), hydatid, hydatidiform (benign) (complicating pregnancy) (delivered) (undelivered), malignant | D39.2 |
| Mole (pigmented), hydatid, hydatidiform (benign) (complicating pregnancy) (delivered) (undelivered), partial | O01.1 |
| Mole (pigmented), intrauterine | O02.0 |
| Mole (pigmented), invasive (hydatidiform) | D39.2 |
| Mole (pigmented), malignant, meaning, malignant hydatidiform mole | D39.2 |
| Mole (pigmented), malignant, meaning, melanoma — see Melanoma | — |
| Mole (pigmented), nonhydatidiform | O02.0 |
| Mole (pigmented), nonpigmented — see Nevus | — |
| Mole (pigmented), pregnancy NEC | O02.0 |
| Mole (pigmented), skin — see Nevus | — |
| Mole (pigmented), tubal | — |
| Mole (pigmented), tubal, with intrauterine pregnancy | — |
| Mole (pigmented), vesicular — see Mole, hydatidiform | — |
| Molimen, molimina (menstrual) | N94.3 |
| Molluscum contagiosum (epitheliale) | B08.1 |
| Mönckeberg's arteriosclerosis, disease, or sclerosis — see Arteriosclerosis, extremities | — |
| Mondini's malformation (cochlea) | Q16.5 |
| Mondor's disease | I80.8 |
| Monge's disease | T70.29 |
| Monilethrix (congenital) | Q84.1 |
| Moniliasis | B37.9 |
| Moniliasis, neonatal | P37.5 |
| Monitoring (encounter for), therapeutic drug level | Z51.81 |
| Monkey malaria | B53.1 |
| Monkeypox | B04 |
| Monoarthritis | M13.10 |
| Monoarthritis, ankle | — |
| Monoarthritis, elbow | — |
| Monoarthritis, foot joint | — |
| Monoarthritis, hand joint | — |
| Monoarthritis, hip | — |
| Monoarthritis, knee | — |
| Monoarthritis, shoulder | — |
| Monoarthritis, wrist | — |
| Monoblastic — see condition | — |
| Monochromat (ism), monochromatopsia (acquired) (congenital) | H53.51 |
| Monocytic — see condition | — |
| Monocytopenia | D72.818 |
| Monocytosis (symptomatic) | D72.821 |
| Monomania — see Psychosis | — |
| Mononeuritis | G58.9 |
| Mononeuritis, cranial nerve — see Disorder, nerve, cranial | — |
| Mononeuritis, femoral nerve | — |
| Mononeuritis, lateral, cutaneous nerve of thigh | — |
| Mononeuritis, lateral, popliteal nerve | — |
| Mononeuritis, lower limb | — |
| Mononeuritis, lower limb, specified nerve NEC | — |
| Mononeuritis, medial popliteal nerve | — |
| Mononeuritis, median nerve | — |
| Mononeuritis, multiplex | G58.7 |
| Mononeuritis, plantar nerve | — |
| Mononeuritis, posterior tibial nerve | — |
| Mononeuritis, radial nerve | — |
| Mononeuritis, sciatic nerve | — |
| Mononeuritis, specified NEC | G58.8 |
| Mononeuritis, tibial nerve | — |
| Mononeuritis, ulnar nerve | — |
| Mononeuritis, upper limb | — |
| Mononeuritis, upper limb, specified nerve NEC | — |
| Mononeuropathy | G58.9 |
| Mononeuropathy, carpal tunnel syndrome — see Syndrome, carpal tunnel | — |
| Mononeuropathy, diabetic NEC — see E08-E13 with .41 | — |
| Mononeuropathy, femoral nerve — see Lesion, nerve, femoral | — |
| Mononeuropathy, ilioinguinal nerve | — |
| Mononeuropathy, intercostal | G58.0 |
| Mononeuropathy, lower limb | — |
| Mononeuropathy, lower limb, causalgia — see Causalgia, lower limb | — |
| Mononeuropathy, lower limb, femoral nerve — see Lesion, nerve, femoral | — |
| Mononeuropathy, lower limb, meralgia paresthetica | — |
| Mononeuropathy, lower limb, plantar nerve — see Lesion, nerve, plantar | — |
| Mononeuropathy, lower limb, popliteal nerve — see Lesion, nerve, popliteal | — |
| Mononeuropathy, lower limb, sciatic nerve — see Lesion, nerve, sciatic | — |
| Mononeuropathy, lower limb, specified NEC | — |
| Mononeuropathy, lower limb, tarsal tunnel syndrome — see Syndrome, tarsal tunnel | — |
| Mononeuropathy, median nerve — see Lesion, nerve, median | — |
| Mononeuropathy, multiplex | G58.7 |
| Mononeuropathy, obturator nerve | — |
| Mononeuropathy, popliteal nerve — see Lesion, nerve, popliteal | — |
| Mononeuropathy, radial nerve — see Lesion, nerve, radial | — |
| Mononeuropathy, saphenous nerve | — |
| Mononeuropathy, specified NEC | G58.8 |
| Mononeuropathy, tarsal tunnel syndrome — see Syndrome, tarsal tunnel | — |
| Mononeuropathy, tuberculous | A17.83 |
| Mononeuropathy, ulnar nerve — see Lesion, nerve, ulnar | — |
| Mononeuropathy, upper limb | — |
| Mononeuropathy, upper limb, carpal tunnel syndrome — see Syndrome, carpal tunnel | — |
| Mononeuropathy, upper limb, causalgia — see Causalgia | — |
| Mononeuropathy, upper limb, median nerve — see Lesion, nerve, median | — |
| Mononeuropathy, upper limb, radial nerve — see Lesion, nerve, radial | — |
| Mononeuropathy, upper limb, specified site NEC | — |
| Mononeuropathy, upper limb, ulnar nerve — see Lesion, nerve, ulnar | — |
| Mononucleosis, infectious | B27.90 |
| Mononucleosis, infectious, cytomegaloviral | B27.10 |
| Mononucleosis, infectious, cytomegaloviral, with, complication NEC | B27.19 |
| Mononucleosis, infectious, cytomegaloviral, with, meningitis | B27.12 |
| Mononucleosis, infectious, cytomegaloviral, with, polyneuropathy | B27.11 |
| Mononucleosis, infectious, Epstein-Barr (virus) | B27.00 |
| Mononucleosis, infectious, Epstein-Barr (virus), with, complication NEC | B27.09 |
| Mononucleosis, infectious, Epstein-Barr (virus), with, meningitis | B27.02 |
| Mononucleosis, infectious, Epstein-Barr (virus), with, polyneuropathy | B27.01 |
| Mononucleosis, infectious, gammaherpesviral | B27.00 |
| Mononucleosis, infectious, gammaherpesviral, with, complication NEC | B27.09 |
| Mononucleosis, infectious, gammaherpesviral, with, meningitis | B27.02 |
| Mononucleosis, infectious, gammaherpesviral, with, polyneuropathy | B27.01 |
| Mononucleosis, infectious, specified NEC | B27.80 |
| Mononucleosis, infectious, specified NEC, with, complication NEC | B27.89 |
| Mononucleosis, infectious, specified NEC, with, meningitis | B27.82 |
| Mononucleosis, infectious, specified NEC, with, polyneuropathy | B27.81 |
| Mononucleosis, infectious, with, complication NEC | B27.99 |
| Mononucleosis, infectious, with, meningitis | B27.92 |
| Mononucleosis, infectious, with, polyneuropathy | B27.91 |
| Monoparesis — see Monoplegia | — |
| Monoplegia | — |
| Monoplegia, congenital (cerebral) | G80.8 |
| Monoplegia, congenital (cerebral), spastic | G80.1 |
| Monoplegia, embolic (current episode) | — |
| Monoplegia, following, cerebrovascular disease, cerebral infarction, lower limb | — |
| Monoplegia, following, cerebrovascular disease, cerebral infarction, upper limb | — |
| Monoplegia, following, cerebrovascular disease, intracerebral hemorrhage, lower limb | — |
| Monoplegia, following, cerebrovascular disease, intracerebral hemorrhage, upper limb | — |
| Monoplegia, following, cerebrovascular disease, lower limb | — |
| Monoplegia, following, cerebrovascular disease, nontraumatic intracranial hemorrhage NEC, lower limb | — |
| Monoplegia, following, cerebrovascular disease, nontraumatic intracranial hemorrhage NEC, upper limb | — |
| Monoplegia, following, cerebrovascular disease, specified disease NEC, lower limb | — |
| Monoplegia, following, cerebrovascular disease, specified disease NEC, upper limb | — |
| Monoplegia, following, cerebrovascular disease, stroke NOS, lower limb | — |
| Monoplegia, following, cerebrovascular disease, stroke NOS, upper limb | — |
| Monoplegia, following, cerebrovascular disease, subarachnoid hemorrhage, lower limb | — |
| Monoplegia, following, cerebrovascular disease, subarachnoid hemorrhage, upper limb | — |
| Monoplegia, following, cerebrovascular disease, upper limb | — |
| Monoplegia, hysterical (transient) | F44.4 |
| Monoplegia, lower limb | — |
| Monoplegia, psychogenic (conversion reaction) | F44.4 |
| Monoplegia, thrombotic (current episode) | — |
| Monoplegia, transient | R29.818 |
| Monoplegia, upper limb | — |
| Monorchism, monorchidism | Q55.0 |
| Monosomy | Q93.9 |
| Monosomy, specified NEC | Q93.89 |
| Monosomy, whole chromosome, meiotic nondisjunction | Q93.0 |
| Monosomy, whole chromosome, mitotic nondisjunction | Q93.1 |
| Monosomy, whole chromosome, mosaicism | Q93.1 |
| Monosomy, X | Q96.9 |
| Monster, monstrosity (single) | Q89.7 |
| Monster, monstrosity (single), acephalic | Q00.0 |
| Monster, monstrosity (single), twin | Q89.4 |
| Monteggia's fracture (-dislocation) | — |
| Moore's syndrome — see Epilepsy, specified NEC | — |
| Mooren's ulcer (cornea) — see Ulcer, cornea, Mooren's | — |
| Mooser-Neill reaction | A75.2 |
| Mooser's bodies | A75.2 |
| Morbidity not stated or unknown | R69 |
| Morbilli — see Measles | — |
| Morbus — see also Disease | — |
| Morbus, angelicus, anglorum | E55.0 |
| Morbus, Beigel | B36.2 |
| Morbus, caducus — see Epilepsy | — |
| Morbus, celiacus | K90.0 |
| Morbus, comitialis — see Epilepsy | — |
| Morbus, cordis | I51.9 |
| Morbus, cordis, valvulorum — see Endocarditis | — |
| Morbus, coxae senilis | M16.9 |
| Morbus, coxae senilis, tuberculous | A18.02 |
| Morbus, hemorrhagicus neonatorum | P53 |
| Morbus, maculosus neonatorum | P54.5 |
| Morel-Kraepelin disease — see Schizophrenia | — |
| Morel-Moore syndrome | M85.2 |
| Morelsyndrome (-Stewart)(-Morgagni) | M85.2 |
| Morgagni-Stewart-Morel syndrome | M85.2 |
| Morgagni-Stokes-Adams syndrome | I45.9 |
| Morgagni-Turnersyndrome (-Albright) | Q96.9 |
| Morgagni's, cyst, organ, hydatid, or appendage, female | Q50.5 |
| Morgagni's, cyst, organ, hydatid, or appendage, male (epididymal) | Q55.4 |
| Morgagni's, cyst, organ, hydatid, or appendage, male (epididymal), testicular | Q55.29 |
| Morgagni's, syndrome | M85.2 |
| Moria | F07.0 |
| Moron (I.Q.50-69) | F70 |
| Morphea | L94.0 |
| Morphinism (without remission) | F11.20 |
| Morphinism (without remission), with remission | F11.21 |
| Morphinomania (without remission) | F11.20 |
| Morphinomania (without remission), with remission | F11.21 |
| Morquiodisease or syndrome (-Ullrich)(-Brailsford) — see Mucopolysaccharidosis | — |
| Mortification (dry) (moist) — see Gangrene | — |
| Morton's metatarsalgia (neuralgia)(neuroma) (syndrome) | — |
| Morvan's disease or syndrome | G60.8 |
| Mosaicism, mosaic (autosomal) (chromosomal), 45,X/46,XX | Q96.3 |
| Mosaicism, mosaic (autosomal) (chromosomal), 45,X/other cell lines NEC with abnormal sex chromosome | Q96.4 |
| Mosaicism, mosaic (autosomal) (chromosomal), sex chromosome, female | Q97.8 |
| Mosaicism, mosaic (autosomal) (chromosomal), sex chromosome, lines with various numbers of X chromosomes | Q97.2 |
| Mosaicism, mosaic (autosomal) (chromosomal), sex chromosome, male | Q98.7 |
| Mosaicism, mosaic (autosomal) (chromosomal), XY | Q96.3 |
| Moschowitz' disease | M31.19 |
| Mother yaw | A66.0 |
| Motion sickness (from travel, any vehicle) (from roundabouts or swings) | T75.3 |
| Mottled, mottling, teeth (enamel) (endemic) (nonendemic) | K00.3 |
| Mounier-Kuhn syndrome | Q32.4 |
| Mounier-Kuhn syndrome, acquired | J98.09 |
| Mounier-Kuhn syndrome, acquired, with bronchiectasis | J47.9 |
| Mounier-Kuhn syndrome, acquired, with bronchiectasis, with, exacerbation (acute) | J47.1 |
| Mounier-Kuhn syndrome, acquired, with bronchiectasis, with, lower respiratory infection | J47.0 |
| Mounier-Kuhn syndrome, with bronchiectasis | J47.9 |
| Mounier-Kuhn syndrome, with bronchiectasis, exacerbation (acute) | J47.1 |
| Mounier-Kuhn syndrome, with bronchiectasis, lower respiratory infection | J47.0 |
| Mountain, sickness | T70.29 |
| Mountain, sickness, with polycythemia , acquired (acute) | D75.1 |
| Mountain, tick fever | A93.2 |
| Mouse, joint — see Loose, body, joint | — |
| Mouse, joint, knee | — |
| Mouth — see condition | — |
| Movable, kidney | N28.89 |
| Movable, kidney, congenital | Q63.8 |
| Movable, spleen | D73.89 |
| Movements, dystonic | R25.8 |
| Moyamoya disease | I67.5 |
| Mpox | B04 |
| MRSA (Methicillin resistant Staphylococcus aureus), infection | A49.02 |
| MRSA (Methicillin resistant Staphylococcus aureus), infection, as the cause of diseases classified elsewhere | B95.62 |
| MRSA (Methicillin resistant Staphylococcus aureus), sepsis | A41.02 |
| MSD (multiple sulfatase deficiency) | E75.26 |
| MSSA (Methicillin susceptible Staphylococcus aureus), infection | A49.01 |
| MSSA (Methicillin susceptible Staphylococcus aureus), infection, as the cause of diseases classified elsewhere | B95.61 |
| MSSA (Methicillin susceptible Staphylococcus aureus), sepsis | A41.01 |
| Mucha-Habermann disease | L41.0 |
| Mucinosis (cutaneous) (focal) (papular) (reticular erythematous) (skin) | L98.5 |
| Mucinosis (cutaneous) (focal) (papular) (reticular erythematous) (skin), oral | K13.79 |
| Mucocele, appendix | K38.8 |
| Mucocele, buccal cavity | K13.79 |
| Mucocele, gallbladder | K82.1 |
| Mucocele, lacrimal sac, chronic | — |
| Mucocele, nasal sinus | J34.1 |
| Mucocele, nose | J34.1 |
| Mucocele, salivary gland (any) | K11.6 |
| Mucocele, sinus (accessory) (nasal) | J34.1 |
| Mucocele, turbinate (bone) (middle) (nasal) | J34.1 |
| Mucocele, uterus | N85.8 |
| Mucolipidosis, I | E77.1 |
| Mucolipidosis, II, III | E77.0 |
| Mucolipidosis, IV | E75.11 |
| Mucopolysaccharidosis | E76.3 |
| Mucopolysaccharidosis, beta-gluduronidase deficiency | E76.29 |
| Mucopolysaccharidosis, cardiopathy | E76.3 |
| Mucopolysaccharidosis, Hunter's syndrome | E76.1 |
| Mucopolysaccharidosis, Hurler-Scheie syndrome | E76.02 |
| Mucopolysaccharidosis, Hurler's syndrome | E76.01 |
| Mucopolysaccharidosis, Maroteaux-Lamy syndrome | E76.29 |
| Mucopolysaccharidosis, Morquio syndrome | E76.219 |
| Mucopolysaccharidosis, Morquio syndrome, A | E76.210 |
| Mucopolysaccharidosis, Morquio syndrome, B | E76.211 |
| Mucopolysaccharidosis, Morquio syndrome, classic | E76.210 |
| Mucopolysaccharidosis, Sanfilippo syndrome | E76.22 |
| Mucopolysaccharidosis, Scheie's syndrome | E76.03 |
| Mucopolysaccharidosis, specified NEC | E76.29 |
| Mucopolysaccharidosis, type, I, Hurler-Scheie syndrome | E76.02 |
| Mucopolysaccharidosis, type, I, Hurler's syndrome | E76.01 |
| Mucopolysaccharidosis, type, I, Scheie's syndrome | E76.03 |
| Mucopolysaccharidosis, type, II | E76.1 |
| Mucopolysaccharidosis, type, III | E76.22 |
| Mucopolysaccharidosis, type, IV | E76.219 |
| Mucopolysaccharidosis, type, IVA | E76.210 |
| Mucopolysaccharidosis, type, IVB | E76.211 |
| Mucopolysaccharidosis, type, VI | E76.29 |
| Mucopolysaccharidosis, type, VII | E76.29 |
| Mucormycosis | B46.5 |
| Mucormycosis, cutaneous | B46.3 |
| Mucormycosis, disseminated | B46.4 |
| Mucormycosis, gastrointestinal | B46.2 |
| Mucormycosis, generalized | B46.4 |
| Mucormycosis, pulmonary | B46.0 |
| Mucormycosis, rhinocerebral | B46.1 |
| Mucormycosis, skin | B46.3 |
| Mucormycosis, subcutaneous | B46.3 |
| Mucositis (ulcerative) | K12.30 |
| Mucositis (ulcerative), due to drugs NEC | K12.32 |
| Mucositis (ulcerative), gastrointestinal | K92.81 |
| Mucositis (ulcerative), mouth (oral) (oropharyngeal) | K12.30 |
| Mucositis (ulcerative), mouth (oral) (oropharyngeal), due to antineoplastic therapy | K12.31 |
| Mucositis (ulcerative), mouth (oral) (oropharyngeal), due to drugs NEC | K12.32 |
| Mucositis (ulcerative), mouth (oral) (oropharyngeal), due to radiation | K12.33 |
| Mucositis (ulcerative), mouth (oral) (oropharyngeal), specified NEC | K12.39 |
| Mucositis (ulcerative), mouth (oral) (oropharyngeal), viral | K12.39 |
| Mucositis (ulcerative), nasal | J34.81 |
| Mucositis (ulcerative), oral cavity — see Mucositis, mouth | — |