autosomal recessive severe congenital neutropenia due to CSF3R deficiency
MONDO:0014865Mondo
Findings
No curated finding names autosomal recessive severe congenital neutropenia due to CSF3R deficiency yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
- Inheritance
- Autosomal recessive inheritance
- Onset and course
- Infantile onset · Neonatal onset · Childhood onset
HPO, annotations 2026-09-02
Features
3 features
What the disease is reported to present with, and how often among people who have it — never how often a feature means the disease. HPO, annotations 2026-09-02.
- Decreased total neutrophil countHPOHP:0001875
- 4 of 4 reported patients
- Recurrent infectionsHPOHP:0002719
- 4 of 4 reported patients
- Bone marrow maturation arrestHPOHP:0033606
- 0 of 3 reported patients
Genes
2 genes
Germline variants in the gene encoding each protein, as classified by GenCC submitters, each in their own words. Limited, disputed and refuted submissions are listed too.
Where it sits
Other names
1 name
Resolves to: autosomal recessive severe congenital neutropenia due to CSF3R deficiency
- Also called
- neutropenia, Severe congenital, 7, autosomal recessive