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Hemic and Lymphatic Diseases: all > Hematologic Diseases [MESH:D006402] > Blood Protein Disorders [MESH:D001796] > Agammaglobulinemia [MESH:D000361] Achondroplasia and Swiss type agammaglobulinemia [MESH:C536020] (1) Agammaglobulinemia, microcephaly, and severe dermatitis [MESH:C538055] (1) Agammaglobulinemia, non-Bruton type [MESH:C538056] (1) Agammaglobulinemia, Non-Bruton Type, Autosomal Dominant [MESH:C563305] (1) Agammaglobulinemia, X-linked, type 2 [MESH:C538057] (1) Bruton type agammaglobulinemia [MESH:C537409] (19) Frenkel Russe syndrome [MESH:C535638] (1) Granulocytopenia with Immunoglobulin Abnormality [MESH:C565535] (1) Hypogammaglobulinemia and Isolated growth hormone deficiency, X-linked [MESH:C537149] (19) Hypogammaglobulinemia, X-Linked [MESH:C562478] (1) more... C16. Congenital, Hereditary, and Neonatal Diseases and Abnormalities (group results) Congenital, Hereditary, and Neonatal Diseases and Abnormalities [MESH:D009358] (149) Z. Exceptions (1) C17. 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These terms define your current search. Click the × to remove a term. C15. Hemic and Lymphatic Diseases: Hematologic Diseases [MESH:D006402] > Blood Protein Disorders [MESH:D001796] > Agammaglobulinemia [MESH:D000361] × 156 items, grouped by C15. Hemic and Lymphatic Diseases (view ungrouped items) Achondroplasia and Swiss type agammaglobulinemia [MESH:C536020] (1)    MESH:C536020   Achondroplasia and Swiss type agammaglobulinemia C536020               Agammaglobulinemia, microcephaly, and severe dermatitis [MESH:C538055] (1)    MESH:C538055   Agammaglobulinemia, microcephaly, and severe dermatitis C538055               Agammaglobulinemia, non-Bruton type [MESH:C538056] (1)    MESH:C538056   Agammaglobulinemia, non-Bruton type C538056               Agammaglobulinemia, Non-Bruton Type, Autosomal Dominant [MESH:C563305] (1)    MESH:C563305   Agammaglobulinemia, Non-Bruton Type, Autosomal Dominant C563305               Agammaglobulinemia, X-linked, type 2 [MESH:C538057] (1)    MESH:C538057   Agammaglobulinemia, X-linked, type 2 C538057               Bruton type agammaglobulinemia [MESH:C537409] (19)    MESH:C028007   nickel monoxide C028007               MESH:C488369   dasatinib C488369               MESH:C537409   Bruton type agammaglobulinemia C537409               MESH:C551803   PCI 32765 C551803               MESH:D001564   Benzo(a)pyrene D001564               MESH:D002118   Calcium D002118               all 19 items... Frenkel Russe syndrome [MESH:C535638] (1)    MESH:C535638   Frenkel Russe syndrome C535638               Granulocytopenia with Immunoglobulin Abnormality [MESH:C565535] (1)    MESH:C565535   Granulocytopenia with Immunoglobulin Abnormality C565535               Hypogammaglobulinemia and Isolated growth hormone deficiency, X-linked [MESH:C537149] (19)    MESH:C028007   nickel monoxide C028007               MESH:C488369   dasatinib C488369               MESH:C537149   Hypogammaglobulinemia and Isolated growth hormone deficiency, X-linked C537149               MESH:C551803   PCI 32765 C551803               MESH:D001564   Benzo(a)pyrene D001564               MESH:D002118   Calcium D002118               all 19 items... Hypogammaglobulinemia, X-Linked [MESH:C562478] (1)    MESH:C562478   Hypogammaglobulinemia, X-Linked C562478               Leukoencephalopathy, Arthritis, Colitis, and Hypogammaglobulinema [MESH:C563852] (1)    MESH:C563852   Leukoencephalopathy, Arthritis, Colitis, and Hypogammaglobulinema C563852               Leukoencephalopathy, arthritis, colitis, and hypogammaglobulinemia [MESH:C535888] (1)    MESH:C535888   Leukoencephalopathy, arthritis, colitis, and hypogammaglobulinemia C535888               Microcephaly with Chemotactic Defect and Transient Hypogammaglobulinemia [MESH:C565381] (1)    MESH:C565381   Microcephaly with Chemotactic Defect and Transient Hypogammaglobulinemia C565381               Osteopetrosis, Autosomal Recessive 7 [MESH:C567354] (36)    MESH:C006253   pirinixic acid C006253               MESH:C006552   kaempferol C006552               MESH:C006632   arsenic trioxide C006632               MESH:C008261   lead acetate C008261               MESH:C009505   4,4'-diaminodiphenylmethane C009505               MESH:C013592   mangiferin C013592               all 36 items... Say Barber Miller syndrome [MESH:C536618] (1)    MESH:C536618   Say Barber Miller syndrome C536618               Severe combined immunodeficiency due to adenosine deaminase deficiency [MESH:C531816] (67)    MESH:C001073   2,4-dinitrobenzenesulfonic acid C001073               MESH:C004925   methylmercuric chloride C004925               MESH:C006253   pirinixic acid C006253               MESH:C009495   titanium dioxide C009495               MESH:C010192   9-(2-hydroxy-3-nonyl)adenine C010192               MESH:C014612   indolebutyric acid C014612               all 67 items...  (others) (38)    MESH:C006780   bisphenol A C006780               MESH:C017096   n-butoxyethanol C017096               MESH:C023036   perfluorooctanoic acid C023036               MESH:C025256   nonylphenol C025256               MESH:C027373   potassium chromate(VI) C027373               MESH:C029341   oxophenylarsine C029341               all 38 items...