| Source | us.nlm.vsac#0.11.0:null (v4.0.1) |
| resourceType | ValueSet |
| id | 2.16.840.1.113762.1.4.1078.491 |
| canonical | http://cts.nlm.nih.gov/fhir/ValueSet/2.16.840.1.113762.1.4.1078.491 |
| version | 20230601 |
| status | active |
| publisher | Optum Steward |
| name | PhagocyticCellDisorders |
| title | Phagocytic Cell Disorders |
| date | 2023-06-01T01:01:19-04:00 |
| description | SCT codes for Phagocytic cell disorders |
| Usages | (none) |
This value set contains 118 concepts
| Code | System | Display |
| 1003381002 | http://snomed.info/sct | Onycho-tricho-dysplasia neutropenia syndrome (disorder) |
| 105601003 | http://snomed.info/sct | Quantitative disorder of neutrophils (disorder) |
| 105602005 | http://snomed.info/sct | Quantitative abnormality of granulocytes (disorder) |
| 111396008 | http://snomed.info/sct | Chédiak-Higashi syndrome (disorder) |
| 111584000 | http://snomed.info/sct | Reticular dysgenesis (disorder) |
| 111585004 | http://snomed.info/sct | Neutropenia associated with autoimmune disease (disorder) |
| 1144929002 | http://snomed.info/sct | Agranulocytosis due to disease (disorder) |
| 1153417000 | http://snomed.info/sct | Secondary hemophagocytic lymphohistiocytosis (disorder) |
| 1156296001 | http://snomed.info/sct | Acquired neutropenia (disorder) |
| 1156300000 | http://snomed.info/sct | Benign ethnic neutropenia (disorder) |
| 1156801007 | http://snomed.info/sct | Macrophage activation syndrome due to juvenile systemic onset arthritis (disorder) |
| 1162505005 | http://snomed.info/sct | Agranulocytosis caused by antithyroid agent (disorder) |
| 1187233008 | http://snomed.info/sct | Leukocyte adhesion deficiency (disorder) |
| 1197482007 | http://snomed.info/sct | Susceptibility to localized juvenile periodontitis (disorder) |
| 1197483002 | http://snomed.info/sct | Functional disorder of polymorphonuclear neutrophil (disorder) |
| 1197594000 | http://snomed.info/sct | Periodic fever, infantile enterocolitis, autoinflammatory syndrome (disorder) |
| 127067009 | http://snomed.info/sct | Stress neutrophilia (disorder) |
| 129639005 | http://snomed.info/sct | Hereditary neutrophilia (disorder) |
| 129641006 | http://snomed.info/sct | Chronic benign neutropenia of childhood (disorder) |
| 129643009 | http://snomed.info/sct | Chronic hypoplastic neutropenia (disorder) |
| 14333004 | http://snomed.info/sct | Alloimmune neonatal neutropenia (disorder) |
| 17182001 | http://snomed.info/sct | Agranulocytosis (disorder) |
| 190959006 | http://snomed.info/sct | Hemophagocytic lymphohistiocytosis due to infection (disorder) |
| 190996002 | http://snomed.info/sct | Severe combined immunodeficiency with reticular dysgenesis (disorder) |
| 191338000 | http://snomed.info/sct | Primary splenic neutropenia (disorder) |
| 191345000 | http://snomed.info/sct | Acquired neutropenia in newborn (disorder) |
| 191347008 | http://snomed.info/sct | Cyclical neutropenia (disorder) |
| 21527007 | http://snomed.info/sct | Chronic granulomatous disease, type IV (disorder) |
| 234423001 | http://snomed.info/sct | Chronic benign neutropenia (disorder) |
| 234424007 | http://snomed.info/sct | Metabolic neutropenia (disorder) |
| 234425008 | http://snomed.info/sct | Autoimmune neutropenia (disorder) |
| 234426009 | http://snomed.info/sct | Corticosteroid-induced neutrophilia (disorder) |
| 234433009 | http://snomed.info/sct | Myeloperoxidase deficiency (disorder) |
| 234436001 | http://snomed.info/sct | Hemolytic erythrophagocytic syndrome (disorder) |
| 234437005 | http://snomed.info/sct | Hemophagocytic lymphohistiocytosis (disorder) |
| 234571003 | http://snomed.info/sct | Warts, hypogammaglobulinemia, infections, and myelokathexis (disorder) |
| 234573000 | http://snomed.info/sct | Phagocytic cell defect (disorder) |
| 234574006 | http://snomed.info/sct | Disorder of phagocytic cell number (disorder) |
| 234576008 | http://snomed.info/sct | Chronic familial neutropenia (disorder) |
| 234577004 | http://snomed.info/sct | Lipochrome histiocytosis - familial (disorder) |
| 234578009 | http://snomed.info/sct | Defective phagocytic cell opsonization (disorder) |
| 234579001 | http://snomed.info/sct | Mannan-binding protein deficiency (disorder) |
| 234580003 | http://snomed.info/sct | Defective phagocytic cell chemotaxis (disorder) |
| 234581004 | http://snomed.info/sct | Defective phagocytic cell adhesion (disorder) |
| 234582006 | http://snomed.info/sct | Leukocyte adhesion deficiency - type 1 (disorder) |
| 234583001 | http://snomed.info/sct | Leukocyte adhesion deficiency - type 2 (disorder) |
| 234585008 | http://snomed.info/sct | Defective phagocytic cell killing (disorder) |
| 234586009 | http://snomed.info/sct | Leukocyte glucose-6-phosphate dehydrogenase deficiency (disorder) |
| 234587000 | http://snomed.info/sct | Neutrophil lactoferrin deficiency (disorder) |
| 234588005 | http://snomed.info/sct | Neutrophil secondary granule deficiency (disorder) |
| 234589002 | http://snomed.info/sct | Glutathione synthetase deficiency (disorder) |
| 234590006 | http://snomed.info/sct | Gluthathione peroxidase deficiency (disorder) |
| 234591005 | http://snomed.info/sct | Combined phagocytic defect (disorder) |
| 247860002 | http://snomed.info/sct | Familial neutropenia (disorder) |
| 248693006 | http://snomed.info/sct | Chronic idiopathic neutropenia (disorder) |
| 24974008 | http://snomed.info/sct | Myelokathexis (disorder) |
| 26252007 | http://snomed.info/sct | Chronic granulomatous disease, type IIA (disorder) |
| 267540007 | http://snomed.info/sct | Neutropenia caused by irradiation (disorder) |
| 276576000 | http://snomed.info/sct | Neutropenia of the small for gestational age baby (disorder) |
| 276628009 | http://snomed.info/sct | Chloramphenicol-induced neutropenia (disorder) |
| 29272001 | http://snomed.info/sct | Chronic granulomatous disease, type I (disorder) |
| 302874002 | http://snomed.info/sct | Phagocytic cell dysfunction (disorder) |
| 303011007 | http://snomed.info/sct | Neutropenic disorder (disorder) |
| 32092008 | http://snomed.info/sct | Toxic neutropenia (disorder) |
| 350353007 | http://snomed.info/sct | De Vaal's syndrome (disorder) |
| 350691000119103 | http://snomed.info/sct | Agranulocytosis due to and following administration of antineoplastic agent (disorder) |
| 351287008 | http://snomed.info/sct | Reticular dysgenesis with congenital aleukocytosis (disorder) |
| 387759001 | http://snomed.info/sct | Chronic granulomatous disease (disorder) |
| 3902000 | http://snomed.info/sct | Non dose-related drug-induced neutropenia (disorder) |
| 398250003 | http://snomed.info/sct | Familial hemophagocytic lymphohistiocytosis (disorder) |
| 40197009 | http://snomed.info/sct | Chronic granulomatous disease, type IA (disorder) |
| 409089005 | http://snomed.info/sct | Febrile neutropenia (disorder) |
| 414850009 | http://snomed.info/sct | Neutrophilia disorder (disorder) |
| 416729007 | http://snomed.info/sct | Neutropenia with acquired immunodeficiency syndrome (disorder) |
| 41814009 | http://snomed.info/sct | Neutropenia with dysgranulopoiesis (disorder) |
| 421312009 | http://snomed.info/sct | Agranulocytosis with acquired immunodeficiency syndrome (disorder) |
| 430478003 | http://snomed.info/sct | Macrophage activation syndrome (disorder) |
| 46359005 | http://snomed.info/sct | Neutropenia associated with infectious disease (disorder) |
| 47144000 | http://snomed.info/sct | Acute neutrophilia (disorder) |
| 47318007 | http://snomed.info/sct | Drug-induced neutropenia (disorder) |
| 55444004 | http://snomed.info/sct | Transient neonatal neutropenia (disorder) |
| 56918001 | http://snomed.info/sct | Dose-related drug-induced neutropenia (disorder) |
| 63484008 | http://snomed.info/sct | Drug-induced neutrophilia (disorder) |
| 65623009 | http://snomed.info/sct | Immune neutropenia (disorder) |
| 70349007 | http://snomed.info/sct | Pseudoneutrophilia (disorder) |
| 713444005 | http://snomed.info/sct | Hemophagocytic syndrome with human immunodeficiency virus infection (disorder) |
| 713530002 | http://snomed.info/sct | Agranulocytosis co-occurrent with human immunodeficiency virus infection (disorder) |
| 71436005 | http://snomed.info/sct | Lazy leukocyte syndrome (disorder) |
| 71610005 | http://snomed.info/sct | Neutrophilic leukemoid reaction (disorder) |
| 718882006 | http://snomed.info/sct | X-linked severe congenital neutropenia (disorder) |
| 720520009 | http://snomed.info/sct | Attenuated Chédiak-Higashi syndrome (disorder) |
| 722925004 | http://snomed.info/sct | Transient neonatal neutropenia due to congenital viral infection (disorder) |
| 722926003 | http://snomed.info/sct | Transient neonatal neutropenia due to neonatal bacterial sepsis (disorder) |
| 725137007 | http://snomed.info/sct | Neutropenia, monocytopenia, deafness syndrome (disorder) |
| 735434003 | http://snomed.info/sct | Acquired neutrophilia (disorder) |
| 735435002 | http://snomed.info/sct | Constitutional neutrophilia (disorder) |
| 76243000 | http://snomed.info/sct | Chronic granulomatous disease, type IVA (disorder) |
| 763668009 | http://snomed.info/sct | Lichtenstein syndrome (disorder) |
| 767658000 | http://snomed.info/sct | Neutropenia due to and following chemotherapy (disorder) |
| 770942003 | http://snomed.info/sct | Kostmann syndrome (disorder) |
| 770947009 | http://snomed.info/sct | Autosomal dominant severe congenital neutropenia (disorder) |
| 772126000 | http://snomed.info/sct | Poikiloderma with neutropenia (disorder) |
| 77330006 | http://snomed.info/sct | Chronic granulomatous disease, type II (disorder) |
| 775909002 | http://snomed.info/sct | Congenital neutropenia, myelofibrosis, nephromegaly syndrome (disorder) |
| 778024005 | http://snomed.info/sct | Monocytopenia with susceptibility to infections (disorder) |
| 782759001 | http://snomed.info/sct | X-linked dyserythropoietic anemia with abnormal platelets and neutropenia (disorder) |
| 782915004 | http://snomed.info/sct | Acquired hemophagocytic lymphohistiocytosis associated with malignant disease (disorder) |
| 783058007 | http://snomed.info/sct | Autosomal recessive severe congenital neutropenia due to glucose-6-phosphatase catalytic subunit 3 deficiency (disorder) |
| 783199003 | http://snomed.info/sct | Autosomal recessive severe congenital neutropenia due to jagunal homolog 1 deficiency (disorder) |
| 783200000 | http://snomed.info/sct | Autosomal recessive severe congenital neutropenia due to C-X-C motif chemokine receptor 2 deficiency (disorder) |
| 783201001 | http://snomed.info/sct | Autosomal recessive severe congenital neutropenia due to colony stimulating factor 3 receptor deficiency (disorder) |
| 78378009 | http://snomed.info/sct | Isoimmune neutropenia (disorder) |
| 784392009 | http://snomed.info/sct | Adult chronic idiopathic neutropenia (disorder) |
| 80255009 | http://snomed.info/sct | Maternal transfer neutropenia (disorder) |
| 80369006 | http://snomed.info/sct | Chronic neutrophilia (disorder) |
| 82317007 | http://snomed.info/sct | Chronic granulomatous disease, type III (disorder) |
| 89454001 | http://snomed.info/sct | Shwachman syndrome (disorder) |
| 89655007 | http://snomed.info/sct | Congenital neutropenia (disorder) |
Produced 08 Sep 2023