Certain infectious and parasitic diseases
Certain infectious and parasitic diseases Certain infectious and parasitic diseases
D81 Combined immunodeficiencies Excludes: autosomal recessive agammaglobulinaemia (Swiss type) ( D80.0 ) D81.0 Severe combined immunodeficiency [SCID] with reticular dysgenesis D81.1 Severe combined immunodeficiency [SCID] with low T- and B-cell numbers D81.2 Severe combined immunodeficiency [SCID] with low or normal B-cell numbers D81.3 Adenosine deaminase [ADA] deficiency D81.4 Nezelof's syndrome D81.5 Purine nucleoside phosphorylase [PNP] deficiency D81.6 Major histocompatibility complex class I deficiency Bare lymphocyte syndrome D81.7 Major histocompatibility complex class II deficiency D81.8 Other combined immunodeficiencies Biotin-dependent carboxylase deficiency D81.9 Combined immunodeficiency, unspecified Severe combined immunodeficiency disorder [SCID] NOS D82 Immunodeficiency associated with other major defects Excludes: ataxia telangiectasia [Louis-Bar] ( G11.3 ) D82.0 Wiskott-Aldrich syndrome Immunodeficiency with thrombocytopenia and eczema D82.1 Di George's syndrome Pharyngeal pouch syndrome Thymic: · alymphoplasia · aplasia or hypoplasia with immunodeficiency D82.2 Immunodeficiency with short-limbed stature D82.3 Immunodeficiency following hereditary defective response to Epstein-Barr virus X-linked lymphoproliferative disease D82.4 Hyperimmunoglobulin E [IgE] syndrome D82.8 Immunodeficiency associated with other specified major defects D82.9 Immunodeficiency associated with major defect, unspecified D83 Common variable immunodeficiency D83.0 Common variable immunodeficiency with predominant abnormalities of B- cell numbers and function D83.1 Common variable immunodeficiency with predominant immunoregulatory T-cell disorders D83.2 Common variable immunodeficiency with autoantibodies to B- or T-cells D83.8 Other common variable immunodeficiencies D83.9 Common variable immunodeficiency, unspecified 138 WHO’s ICD-10
D84 Other immunodeficiencies D84.0 Lymphocyte function antigen-1 [LFA-1] defect D84.1 Defects in the complement system C1 esterase inhibitor [C1-INH] deficiency D84.8 Other specified immunodeficiencies D84.9 Immunodeficiency, unspecified D86 Sarcoidosis D86.0 Sarcoidosis of lung D86.1 Sarcoidosis of lymph nodes D86.2 Sarcoidosis of lung with sarcoidosis of lymph nodes D86.3 Sarcoidosis of skin D86.8 Sarcoidosis of other and combined sites Iridocyclitis in sarcoidosis† ( H22.1* ) Multiple cranial nerve palsies in sarcoidosis† ( G53.2* ) Sarcoid: · arthropathy† ( M14.8* ) · myocarditis† ( I41.8* ) · myositis† ( M63.3* ) Uveoparotid fever [Heerfordt] D86.9 Sarcoidosis, unspecified D89 Other disorders involving the immune mechanism, not elsewhere classified Excludes: hyperglobulinaemia NOS ( R77.1 ) monoclonal gammopathy ( D47.2 ) transplant failure and rejection ( T86.- ) D89.0 Polyclonal hypergammaglobulinaemia Benign hypergammaglobulinaemic purpura Polyclonal gammopathy NOS D89.1 Cryoglobulinaemia Cryoglobulinaemia: · essential · idiopathic · mixed · primary · secondary Cryoglobulinaemic: · purpura · vasculitis D89.2 Hypergammaglobulinaemia, unspecified D89.8 Other specified disorders involving the immune mechanism, not elsewhere classified D89.9 Disorder involving the immune mechanism, unspecified Immune disease NOS Version for 2007 139
- Page 87 and 88: C39 Malignant neoplasm of other and
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- Page 91 and 92: C49 Malignant neoplasm of other con
- Page 93 and 94: C53.8 Overlapping lesion of cervix
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- Page 97 and 98: C71.6 Cerebellum C71.7 Brain stem F
- Page 99 and 100: C77 Secondary and unspecified malig
- Page 101 and 102: C83 Diffuse non-Hodgkin's lymphoma
- Page 103 and 104: C92.0 Acute myeloid leukaemia Exclu
- Page 105 and 106: In situ neoplasms (D00-D09) Note: M
- Page 107 and 108: D04 Carcinoma in situ of skin Exclu
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- Page 111 and 112: D14 Benign neoplasm of middle ear a
- Page 113 and 114: D19.7 Mesothelial tissue of other s
- Page 115 and 116: D23.0 Skin of lip Excludes: vermili
- Page 117 and 118: D30.7 Other urinary organs Parauret
- Page 119 and 120: Neoplasms of uncertain or unknown b
- Page 121 and 122: D40 Neoplasm of uncertain or unknow
- Page 123 and 124: D47.2 Monoclonal gammopathy D47.3 E
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- Page 127 and 128: D53.9 Nutritional anaemia, unspecif
- Page 129 and 130: D59 Acquired haemolytic anaemia D59
- Page 131 and 132: D64.0 Hereditary sideroblastic anae
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- Page 135 and 136: D72.1 Eosinophilia Eosinophilia: ·
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- Page 141 and 142: E00.1 Congenital iodine-deficiency
- Page 143 and 144: E06 Thyroiditis Excludes: postpartu
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- Page 157 and 158: E59 E60 Dietary selenium deficiency
- Page 159 and 160: E70.1 Other hyperphenylalaninaemias
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- Page 163 and 164: E76 Disorders of glycosaminoglycan
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- Page 167 and 168: E86 Volume depletion Dehydration De
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- Page 171 and 172: F02* Dementia in other diseases cla
- Page 173 and 174: F05.8 Other delirium Delirium of mi
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- Page 185 and 186: F25.2 Schizoaffective disorder, mix
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D81 Combined immunodeficiencies<br />
Excludes: autosomal recessive agammaglobulinaemia (Swiss type) ( D80.0 )<br />
D81.0 Severe combined immunodeficiency [SCID] with reticular dysgenesis<br />
D81.1 Severe combined immunodeficiency [SCID] with low T- <strong>and</strong> B-cell numbers<br />
D81.2 Severe combined immunodeficiency [SCID] with low or normal B-cell numbers<br />
D81.3 Adenosine deaminase [ADA] deficiency<br />
D81.4 Nezelof's syndrome<br />
D81.5 Purine nucleoside phosphorylase [PNP] deficiency<br />
D81.6 Major histocompatibility complex class I deficiency<br />
Bare lymphocyte syndrome<br />
D81.7 Major histocompatibility complex class II deficiency<br />
D81.8 Other combined immunodeficiencies<br />
Biotin-dependent carboxylase deficiency<br />
D81.9 Combined immunodeficiency, unspecified<br />
Severe combined immunodeficiency disorder [SCID] NOS<br />
D82 Immunodeficiency associated with other major defects<br />
Excludes: ataxia telangiectasia [Louis-Bar] ( G11.3 )<br />
D82.0 Wiskott-Aldrich syndrome<br />
Immunodeficiency with thrombocytopenia <strong>and</strong> eczema<br />
D82.1 Di George's syndrome<br />
Pharyngeal pouch syndrome<br />
Thymic:<br />
· alymphoplasia<br />
· aplasia or hypoplasia with immunodeficiency<br />
D82.2 Immunodeficiency with short-limbed stature<br />
D82.3 Immunodeficiency following hereditary defective response to Epstein-Barr<br />
virus<br />
X-linked lymphoproliferative disease<br />
D82.4 Hyperimmunoglobulin E [IgE] syndrome<br />
D82.8 Immunodeficiency associated with other specified major defects<br />
D82.9 Immunodeficiency associated with major defect, unspecified<br />
D83 Common variable immunodeficiency<br />
D83.0 Common variable immunodeficiency with predominant abnormalities of B-<br />
cell numbers <strong>and</strong> function<br />
D83.1 Common variable immunodeficiency with predominant immunoregulatory<br />
T-cell disorders<br />
D83.2 Common variable immunodeficiency with autoantibodies to B- or T-cells<br />
D83.8 Other common variable immunodeficiencies<br />
D83.9 Common variable immunodeficiency, unspecified<br />
138 WHO’s ICD-10
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