genetic infantile agranulocytosis
Term · Oncology and biomedicine · MLC-T-ONC-003487
An inherited disorder in which there is a lower-than-normal number of neutrophils (a type of white blood cell that is important in fighting infections). Infants with the disorder get infections caused by bacteria, and are at an increased risk of acute myelogenous leukemia (AML) or myelodysplasia (a bone marrow disorder). Also called congenital neutropenia, infantile genetic agranulocytosis, Kostmann disease, Kostmann neutropenia, and Kostmann syndrome.
| Identifier | MLC-T-ONC-003487 |
|---|---|
| Field | Oncology and biomedicine |
| Synonyms | congenital neutropenia; infantile genetic agranulocytosis; Kostmann disease; Kostmann neutropenia; Kostmann syndrome |
| References | NCI Dictionary of Cancer Terms |
Record as JSON
{
"id": "MLC-T-ONC-003487",
"term": "genetic infantile agranulocytosis",
"field": "Oncology and biomedicine",
"definition": "An inherited disorder in which there is a lower-than-normal number of neutrophils (a type of white blood cell that is important in fighting infections). Infants with the disorder get infections caused by bacteria, and are at an increased risk of acute myelogenous leukemia (AML) or myelodysplasia (a bone marrow disorder). Also called congenital neutropenia, infantile genetic agranulocytosis, Kostmann disease, Kostmann neutropenia, and Kostmann syndrome.",
"synonyms": [
"congenital neutropenia",
"infantile genetic agranulocytosis",
"Kostmann disease",
"Kostmann neutropenia",
"Kostmann syndrome"
],
"references": [
"NCI Dictionary of Cancer Terms"
],
"url": "https://mlchart.com/terminology/oncology/genetic-infantile-agranulocytosis/"
}
Record 7,907 of 17,721 in Oncology and biomedicine terminology (MLC-0111). Request the full dataset.