Hereditary white blood cell disorder (disorder)
| Code | 414395005 |
|---|---|
| Semantic tag | disorder |
| Module | international |
| Definition | defined |
| Effective time | 20050131 |
414393003Hereditary disorder of cellular element of blood
disorder
363138005Hereditary disorder of immune system
disorder
54097007White blood cell disorder
disorder
1332385000AMeD syndrome
disorder
768556005Ataxia pancytopenia syndrome
disorder
111396008Chédiak-Higashi syndrome
disorder
1197428008Combined immunodeficiency, enteropathy spectrum
disorder
775909002Congenital neutropenia, myelofibrosis, nephromegaly syndrome
disorder
398250003Familial haemophagocytic lymphohistiocytosis
disorder
30575002Fanconi's anaemia
disorder
234589002Glutathione synthetase deficiency
disorder
722453009Hennekam Beemer syndrome
disorder
191358004Hereditary eosinophilia
disorder
234435002Hereditary hypersegmentation
disorder
783255002Hereditary isolated aplastic anaemia
disorder
129639005Hereditary neutrophilia
disorder
402794002Heritable disorder of neutrophil function
disorder
402793008Heritable disorder of neutrophil production
disorder
1186654001Immune dysregulation, inflammatory bowel disease, arthritis, recurrent infection, lymphopenia syndrome
disorder
1187233008Leucocyte adhesion deficiency
disorder
1360083000NOCARH syndrome
disorder
1003381002Onycho-tricho-dysplasia neutropenia syndrome
disorder
774071007Pancytopenia with developmental delay syndrome
disorder
71436005Periodic fever, immunodeficiency, thrombocytopenia syndrome
disorder
1197594000Periodic fever, infantile enterocolitis, autoinflammatory syndrome
disorder
772126000Poikiloderma with neutropenia
disorder
111584000Reticular dysgenesis
disorder
723512008Revesz syndrome
disorder
190996002Severe combined immunodeficiency with reticular dysgenesis
disorder
1237618009Short stature, optic nerve atrophy, Pelger-Huët anomaly syndrome
disorder
89454001Shwachman syndrome
disorder
719019000WT limb blood syndrome
disorder
234571003Warts, hypogammaglobulinaemia, infections, and myelokathexis
disorder
782759001X-linked dyserythropoietic anaemia with abnormal platelets and neutropenia
disorder