Hereditary elliptocytosis (disorder)
| Code | 191169008 |
|---|---|
| Semantic tag | disorder |
| Module | international |
| Definition | defined |
| Effective time | 20200131 |
111575000Anaemia due to membrane defect
disorder
42601008Congenital haemolytic anaemia
disorder
276654001Congenital malformation
disorder
363070008Developmental hereditary disorder
disorder
234409003Erythrocyte membrane abnormality
disorder
38911009Hereditary haemolytic anaemia
disorder
720982007Alport syndrome, intellectual disability, midface hypoplasia, elliptocytosis syndrome
disorder
75443009Hereditary elliptocytosis due to abnormal protein 4.1
disorder
8857001Hereditary elliptocytosis due to alpha spectrin defect
disorder
73073009Hereditary elliptocytosis due to beta spectrin defect in self-association
disorder
66262001Hereditary elliptocytosis due to beta spectrin-ankyrin interaction
disorder
5994005Hereditary elliptocytosis due to deficiency of protein 4.1
disorder
15121005Hereditary elliptocytosis due to glycophorin C deficiency
disorder
234410008Hereditary elliptocytosis with transient poikilocytosis
disorder
9434008Hereditary pyropoikilocytosis
disorder
1153399000Homozygous hereditary elliptocytosis
disorder