Hereditary nonspherocytic hemolytic anemia (disorder)
| Code | 301317008 |
|---|---|
| Semantic tag | disorder |
| Module | international |
| Definition | primitive |
| Effective time | 20020131 |
38911009Hereditary haemolytic anaemia
disorder
363041004Congenital nonspherocytic haemolytic anaemia due to inborn error of metabolism
disorder
74703006HNSHA (hereditary nonspherocytic haemolytic anaemia) due to pyruvate kinase deficiency
disorder
47526003HNSHA due to NADH diaphorase deficiency
disorder
78908001HNSHA due to decreased adenosine deaminase activity
disorder
62268000HNSHA due to diphosphoglycerate mutase deficiency
disorder
25251008HNSHA due to gamma glutamyl cysteine synthetase deficiency
disorder
52413004HNSHA due to glucose phosphate isomerase deficiency
disorder
52212006HNSHA due to glutathione reductase deficiency
disorder
111579006HNSHA due to glutathione synthetase deficiency
disorder
42484009HNSHA due to hexokinase deficiency
disorder
41387000HNSHA due to phosphofructokinase deficiency
disorder
59644002HNSHA due to phosphoglycerate kinase deficiency
disorder
34194007HNSHA due to pyrimidine-5'-nucleotidase deficiency
disorder
44641000HNSHA due to triosephosphate isomerase deficiency
disorder
766982000Haemolytic anaemia due to adenylate kinase deficiency
disorder
5315003Haemolytic anaemia due to erythrocyte adenosine deaminase overproduction
disorder
719402008Lethal haemolytic anaemia and genital anomaly syndrome
disorder
725057008Nonspherocytic haemolytic anaemia due to deficiency of adenosinetriphosphatase
disorder