Kostmann syndrome
Term · Oncology and biomedicine · MLC-T-ONC-004663
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, genetic infantile agranulocytosis, infantile genetic agranulocytosis, Kostmann disease, and Kostmann neutropenia.
| Identifier | MLC-T-ONC-004663 |
|---|---|
| Field | Oncology and biomedicine |
| Synonyms | congenital neutropenia; genetic infantile agranulocytosis; infantile genetic agranulocytosis; Kostmann disease; Kostmann neutropenia |
| References | NCI Dictionary of Cancer Terms |
Record as JSON
{
"id": "MLC-T-ONC-004663",
"term": "Kostmann syndrome",
"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, genetic infantile agranulocytosis, infantile genetic agranulocytosis, Kostmann disease, and Kostmann neutropenia.",
"synonyms": [
"congenital neutropenia",
"genetic infantile agranulocytosis",
"infantile genetic agranulocytosis",
"Kostmann disease",
"Kostmann neutropenia"
],
"references": [
"NCI Dictionary of Cancer Terms"
],
"url": "https://mlchart.com/terminology/oncology/kostmann-syndrome/"
}
Record 9,800 of 17,717 in Oncology and biomedicine terminology (MLC-0111). Request the full dataset.