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C15. Hemic and Lymphatic Diseases: all > Hematologic Diseases [MESH:D006402] > Anemia [MESH:D000740] > Anemia, Hemolytic [MESH:D000743] > Anemia, Hemolytic, Congenital [MESH:D000745]

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C15. Hemic and Lymphatic Diseases: Hematologic Diseases [MESH:D006402] > Anemia [MESH:D000740] > Anemia, Hemolytic [MESH:D000743] > Anemia, Hemolytic, Congenital [MESH:D000745]
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2001 items, grouped by C15. Hemic and Lymphatic Diseases (view ungrouped items)

Anemia, Dyserythropoietic, Congenital [MESH:D000742] (81)   
MESH:C002950
 methylformamide
C002950
 
  
  
  
MESH:C004648
 testosterone enanthate
C004648
 
  
  
  
MESH:C005961
 bis(tri-n-butyltin)oxide
C005961
 
  
  
  
MESH:C006253
 pirinixic acid
C006253
 
  
  
  
MESH:C006780
 bisphenol A
C006780
 
  
  
  
MESH:C009495
 titanium dioxide
C009495
 
  
  
  
all 81 items...

Anemia, Hemolytic, Congenital Nonspherocytic [MESH:D000746] (308)   
MESH:C001864
 aluminum phosphide
C001864
 
  
  
  
MESH:C002202
 4-oxoretinoic acid
C002202
 
  
  
  
MESH:C003371
 suxibuzone
C003371
 
  
  
  
MESH:C005273
 naringenin
C005273
 
  
  
  
MESH:C005274
 naringin
C005274
 
  
  
  
MESH:C005310
 norfenefrine
C005310
 
  
  
  
all 308 items...

Anemia, hereditary spherocytic hemolytic [MESH:C536356] (1)   
MESH:C536356
 Anemia, hereditary spherocytic hemolytic
C536356
 
  
  
  

Anemia, Sickle Cell [MESH:D000755] (1722)   
MESH:C000188
 alachlor
C000188
 
  
  
  
MESH:C000228
 aristolochic acid I
C000228
 
  
  
  
MESH:C000488
 cladosporin
C000488
 
  
  
  
MESH:C000499
 ferric oxide
C000499
 
  
  
  
MESH:C001073
 2,4-dinitrobenzenesulfonic acid
C001073
 
  
  
  
MESH:C001277
 geldanamycin
C001277
 
  
  
  
all 1722 items...

Dehydrated Hereditary Stomatocytosis, Pseudohyperkalemia, and Perinatal Edema [MESH:C566369] (1)   
MESH:C566369
 Dehydrated Hereditary Stomatocytosis, Pseudohyperkalemia, and Perinatal Edema
C566369
 
  
  
  

Elliptocytosis, Hereditary [MESH:D004612] (95)   
MESH:C006253
 pirinixic acid
C006253
 
  
  
  
MESH:C006632
 arsenic trioxide
C006632
 
  
  
  
MESH:C006780
 bisphenol A
C006780
 
  
  
  
MESH:C008261
 lead acetate
C008261
 
  
  
  
MESH:C008461
 methyl isocyanate
C008461
 
  
  
  
MESH:C009277
 sodium arsenate
C009277
 
  
  
  
all 95 items...

Glucosephosphate Dehydrogenase Deficiency [MESH:D005955] (196)   
MESH:C001864
 aluminum phosphide
C001864
 
  
  
  
MESH:C002202
 4-oxoretinoic acid
C002202
 
  
  
  
MESH:C005273
 naringenin
C005273
 
  
  
  
MESH:C005274
 naringin
C005274
 
  
  
  
MESH:C005310
 norfenefrine
C005310
 
  
  
  
MESH:C006632
 arsenic trioxide
C006632
 
  
  
  
all 196 items...

Heinz Body Anemias [MESH:C563030] (127)   
MESH:C000188
 alachlor
C000188
 
  
  
  
MESH:C002741
 N-nitrosomorpholine
C002741
 
  
  
  
MESH:C006253
 pirinixic acid
C006253
 
  
  
  
MESH:C006552
 kaempferol
C006552
 
  
  
  
MESH:C006632
 arsenic trioxide
C006632
 
  
  
  
MESH:C006780
 bisphenol A
C006780
 
  
  
  
all 127 items...

Hemoglobin C Disease [MESH:D006445] (2)   
MESH:C531699
 Hb C disease
C531699
 
  
  
  
MESH:D006445
 Hemoglobin C Disease
D006445
 
  
  
  

Hemolytic Anemia, Congenital, with Emphysema and Cutis Laxa [MESH:C562629] (1)   
MESH:C562629
 Hemolytic Anemia, Congenital, with Emphysema and Cutis Laxa
C562629
 
  
  
  

Hemolytic Anemia, Lethal Congenital Nonspherocytic, with Genital and Other Abnormalities [MESH:C563935] (1)   
MESH:C563935
 Hemolytic Anemia, Lethal Congenital Nonspherocytic, with Genital and Other Abnormalities
C563935
 
  
  
  

Red cell phospholipid defect with hemolysis [MESH:C535298] (1)   
MESH:C535298
 Red cell phospholipid defect with hemolysis
C535298
 
  
  
  

Rh-Null Disease, Amorph Type [MESH:C566210] (1)   
MESH:C566210
 Rh-Null Disease, Amorph Type
C566210
 
  
  
  

Spherocytosis, Hereditary [MESH:D013103] (137)   
MESH:C004648
 testosterone enanthate
C004648
 
  
  
  
MESH:C004768
 4,5-dihydroorotic acid
C004768
 
  
  
  
MESH:C006253
 pirinixic acid
C006253
 
  
  
  
MESH:C006632
 arsenic trioxide
C006632
 
  
  
  
MESH:C006780
 bisphenol A
C006780
 
  
  
  
MESH:C008261
 lead acetate
C008261
 
  
  
  
all 137 items...

Stomatocytosis I [MESH:C566111] (1)   
MESH:C566111
 Stomatocytosis I
C566111
 
  
  
  

Stomatocytosis II [MESH:C566110] (1)   
MESH:C566110
 Stomatocytosis II
C566110
 
  
  
  

Thalassemia [MESH:D013789] (501)   
MESH:C000188
 alachlor
C000188
 
  
  
  
MESH:C000515
 cremophor EL
C000515
 
  
  
  
MESH:C001335
 hexachlorobutadiene
C001335
 
  
  
  
MESH:C001803
 tempol
C001803
 
  
  
  
MESH:C002202
 4-oxoretinoic acid
C002202
 
  
  
  
MESH:C002741
 N-nitrosomorpholine
C002741
 
  
  
  
all 501 items...

Transient erythroblastopenia of childhood [MESH:C536980] (1)   
MESH:C536980
 Transient erythroblastopenia of childhood
C536980
 
  
  
  

Uridine 5-Prime Monophosphate Hydrolase Deficiency, Hemolytic Anemia due to [MESH:C564859] (11)   
MESH:C006780
 bisphenol A
C006780
 
  
  
  
MESH:C016403
 2,4-dinitrotoluene
C016403
 
  
  
  
MESH:C023514
 2,6-dinitrotoluene
C023514
 
  
  
  
MESH:C029938
 nickel sulfate
C029938
 
  
  
  
MESH:C564859
 Uridine 5-Prime Monophosphate Hydrolase Deficiency, Hemolytic Anemia due to
C564859
 
  
  
  
MESH:D003993
 Dibutyl Phthalate
D003993
 
  
  
  
all 11 items...

Xerocytosis, hereditary [MESH:C536764] (1)   
MESH:C536764
 Xerocytosis, hereditary
C536764
 
  
  
  

 (others) (1)   
MESH:D000745
 Anemia, Hemolytic, Congenital
D000745