Certain infectious and parasitic diseases

WHO’s ICD-10 version for 2007
Hematuria (essential) R31
- benign (familial) (of childhood) (see also
Hematuria, idiopathic) N02.-
- endemic (see also Schistosomiasis) B65.0
- idiopathic N02.-
- - with glomerular lesion
- - - focal and segmental hyalinosis or
sclerosis N02.1
- - - membranoproliferative (diffuse) N02.5
- - - membranous (diffuse) N02.2
- - - mesangial proliferative (diffuse) N02.3
- - - mesangiocapillary (diffuse) N02.5
- - - proliferative NEC N02.8
- - - specified pathology NEC N02.8
- intermittent (see also Hematuria, idiopathic)
N02.-
- malarial B50.8
- paroxysmal (see also Hematuria, idiopathic)
N02.-
- - nocturnal D59.5
- persistent (see also Hematuria, idiopathic)
N02.-
- recurrent (see also Hematuria, idiopathic)
N02.-
- sulfonamide(s)
- - correct substance properly administered
R31
- - overdose or wrong substance given or
taken T37.0
- tropical (see also Schistosomiasis) B65.0
- tuberculous A18.1
Hemeralopia (day blindness) H53.1
- vitamin A deficiency E50.5† H58.1*
Hemianalgesia R20.0
Hemianencephaly Q00.0
Hemianesthesia R20.0
Hemianopia, hemianopsia (binasal)
(bitemporal) (heteronymous)
(homonymous) (nasal) (peripheral) H53.4
- syphilitic A52.7† H58.1*
Hemiathetosis R25.8
Hemiatrophy R68.8
- cerebellar G31.9
- face, facial, progressive (Romberg) G51.8
- tongue K14.8
Hemiballism(us) G25.5
Hemicardia Q24.8
Hemicephalus, hemicephaly Q00.0
Hemichorea G25.5
Hemicrania
- congenital malformation Q00.0
- meaning migraine G43.9
- paroxysmal, chronic G44.0
Hemidystrophy — see Hemiatrophy
Hemiectromelia Q73.8
Hemihypalgesia R20.8
Hemihypesthesia R20.1
Hemimelia Q73.8
- lower limb Q72.8
- upper limb Q71.8
Hemiparalysis (see also Hemiplegia) G81.9
Hemiparesis (see also Hemiplegia) G81.9
Hemiparesthesia R20.2
Hemiparkinsonism G20
Hemiplegia G81.9
- alternans facialis G83.8
- ascending NEC G81.9
- - spinal G95.8
- congenital (cerebral) G80.8
- - spastic G80.2
- embolic (current episode) I63.4
- flaccid G81.0
- hysterical F44.4
- newborn NEC P91.8
- - birth injury P11.9
- spastic G81.1
- - congenital G80.2
- spinal G81.1
- thrombotic (current episode) I63.3
Hemisection, spinal cord — see Injury,
spinal cord, by region
Hemispasm (facial) R25.2
Hemisporosis B48.8
Hemitremor R25.1
Hemivertebra Q76.4
- failure of segmentation with scoliosis Q76.3
- fusion with scoliosis Q76.3
Hemochromatosis (diabetic) (hereditary)
(liver) (myocardium) (primary idiopathic)
(secondary) E83.1
- with refractory anemia (M9982/1) D46.1
Hemodialysis Z49.1
- preparatory care only (without treatment) Z49.0
Hemoglobin — see also condition
- abnormal (disease) — see Disease, hemoglobin
- AS genotype D57.3
- fetal, hereditary persistence (HPFH) D56.4
- low NEC D64.9
- S (Hb S), heterozygous D57.3
Hemoglobinemia D59.9
- due to blood transfusion T80.8
- paroxysmal D59.6
- - nocturnal D59.5
Hemoglobinopathy (mixed) NEC D58.2
- with thalassemia D56.9
- sickle-cell D57.1
- - with thalassemia D56.8
Hemoglobinuria R82.3
- with anemia, hemolytic, acquired (chronic) NEC
D59.6
- cold (agglutinin) (paroxysmal) (with Raynaud's
syndrome) D59.6
- due to exertion or hemolysis NEC D59.6
- intermittent D59.6
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