Certain infectious and parasitic diseases

WHO’s ICD-10 version for 2007
Monoplegia------continued
- infantile (cerebral) (spinal) G80.8
- lower limb G83.1
- psychogenic (conversion reaction) F44.4
- thrombotic (current episode) I63.3
- transient R29.8
- upper limb G83.2
Monorchism, monorchidism Q55.0
Monosomy (see also Deletion, chromosome)
Q93.9
- specified NEC Q93.8
- whole chromosome
- - meiotic nondisjunction Q93.0
- - mitotic nondisjunction Q93.1
- - mosaicism Q93.1
- X Q96.9
Monster, monstrosity (single) Q89.7
- acephalic Q00.0
- twin Q89.4
Monteggia's fracture(-dislocation) S52.0
Mooren's ulcer (cornea) H16.0
Moore's syndrome G40.8
Mooser's bodies A75.2
Morax-Axenfeld conjunctivitis H10.2
Morbidity, unknown cause R69
Morbilli — see Measles
Morbus (see also Disease)
- caducus (see also Epilepsy) G40.9
- comitialis (see also Epilepsy) G40.9
- cordis (see also Disease, heart) I51.9
- - valvulorum — see Endocarditis
- coxae senilis M16.9
- - tuberculous A18.0† M01.1*
Morel(-Stewart)(-Morgagni) syndrome
M85.2
Morel-Kraepelin disease (see also
Schizophrenia) F20.9
Morgagni's
- cyst, organ, hydatid or appendage
- - female Q50.5
- - male (epididymal) Q55.4
- - - testicular Q55.2
- syndrome M85.2
Morgagni-Stokes-Adams syndrome I45.9
Morgagni-Turner(-Albright) syndrome
Q96.9
Moria F07.0
Moron (I.Q. 50–69) F70.-
Morphea L94.0
Morphinism F11.2
Morphinomania F11.2
Morquio(-Ullrich)(-Brailsford) disease or
syndrome E76.2
Mortality, unknown cause R99
Mortification (dry) (moist) (see also
Gangrene) R02
Morton's metatarsalgia (neuralgia) (neuroma)
G57.6
Morvan's disease or syndrome G60.8
Mosaicism, mosaic (autosomal) (chromosomal)
- sex chromosome
- - female NEC Q97.8
- - - lines with various numbers of X
chromosomes Q97.2
- - male NEC Q98.7
- 45,X
- - cell lines with abnormal sex chromosome
Q96.4
- - 46,XX Q96.3
- - 46,XY Q96.3
Moschowitz' disease M31.1
Motion sickness (from any vehicle) T75.3
Mottled, mottling, teeth (enamel) K00.3
Mountain sickness T70.2
Mouse, joint M24.0
- knee M23.4
Mouth — see condition
Movable
- coccyx M53.2
- kidney N28.8
- - congenital Q63.8
- spleen D73.8
Movements, dystonic R25.8
Moyamoya disease I67.5
Mucha-Habermann disease L41.0
Mucinosis (cutaneous) (focal) (papular) (skin) L98.5
- oral K13.7
Mucocele
- appendix K38.8
- buccal cavity K13.7
- gallbladder K82.1
- lacrimal sac H04.4
- nasal sinus J34.1
- salivary gland (any) K11.6
- sinus (accessory) (nasal) J34.1
- turbinate (bone) (middle) (nasal) J34.1
Mucolipidosis
- I E77.1
- II, III E77.0
- IV E75.1
Mucopolysaccharidosis E76.3
- cardiopathy E76.3† I52.8*
- specified NEC E76.2
- type
- - I E76.0
- - II E76.1
- - III, IV, VI, VII E76.2
Mucormycosis B46.5
- cutaneous B46.3† L99.8*
- disseminated B46.4
- gastrointestinal B46.2† K93.8*
- generalized B46.4
- pulmonary B46.0† J99.8*
373