Disease, diseased - see also Syndrome |
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blood (group) (Duffy) (Kell) (Kidd) (Lewis) (M) (S) NEC 773.2 |
Rh (blood group) (factor) 773.0 |
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unstable hemoglobin 282.7 |
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Henoch (-Schönlein) (purpura nervosa) 287.0 |
hepatic - see Disease, liver |
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heredodegenerative NEC |
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Hers' (glycogenosis VI) 271.0 |
Herter (-Gee) (-Heubner) (nontropical sprue) 579.0 |
Herxheimer's (diffuse idiopathic cutaneous atrophy) 701.8 |
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Heubner-Herter (nontropical sprue) 579.0 |
high fetal gene or hemoglobin thalassemia 282.49 |
Hildenbrand's (typhus) 081.9 |
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tuberculous (see also Tuberculosis) 015.1 [730.85] |
Hippel's (retinocerebral angiomatosis) 759.6 |
Hirschfeld's (acute diabetes mellitus) (see also Diabetes) 250.0 |
due to secondary diabetes 249.0 |
Hirschsprung's (congenital megacolon) 751.3 |
His (-Werner) (trench fever) 083.1 |
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Hodgkin's (M9650/3) 201.9 |
Note22 Use the following fifth-digit subclassification with category 201: 0 unspecified site 1 lymph nodes of head, face, and neck 2 intrathoracic lymph nodes 3 intra-abdominal lymph nodes 4 lymph nodes of axilla and upper limb 5 lymph nodes of inguinal region and lower limb 6 intrapelvic lymph nodes 7 spleen 8 lymph nodes of multiple sites
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lymphocytic |
depletion (M9653/3) 201.7 |
diffuse fibrosis (M9654/3) 201.7 |
reticular type (M9655/3) 201.7 |
predominance (M9651/3) 201.4 |
lymphocytic-histiocytic predominance (M9651/3) 201.4 |
mixed cellularity (M9652/3) 201.6 |
nodular sclerosis (M9656/3) 201.5 |
cellular phase (M9657/3) 201.5 |
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Hoffa (-Kastert) (liposynovitis prepatellaris) 272.8 |
Holla (see also Spherocytosis) 282.0 |
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hookworm (see also Ancylostomiasis) 126.9 |
Horton's (temporal arteritis) 446.5 |
host-versus-graft (immune or nonimmune cause) 279.50 |
HPFH (hereditary persistence of fetal hemoglobin) ("Swiss variety") 282.7 |
Huchard's (continued arterial hypertension) 401.9 |
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