congenital neutropenia-myelofibrosis-nephromegaly syndrome
MONDO:0014118Mondo
Findings
No curated finding names congenital neutropenia-myelofibrosis-nephromegaly syndrome 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
HPO, annotations 2026-09-02
Features
13 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.
- AnemiaHPOHP:0001903
- 7 of 7 reported patients
- Chronic diarrheaHPOHP:0002028
- 7 of 7 reported patients
- Decreased total neutrophil countHPOHP:0001875
- 7 of 7 reported patients
- Enlarged kidneyHPOHP:0000105
- 7 of 7 reported patients
- Extramedullary hematopoiesisHPOHP:0001978
- 5 of 5 reported patients
- Failure to thriveHPOHP:0001508
- 7 of 7 reported patients
- HepatomegalyHPOHP:0002240
- 7 of 7 reported patients
- Increased circulating immunoglobulin concentrationHPOHP:0010702
- 7 of 7 reported patients
- Recurrent infectionsHPOHP:0002719
- 7 of 7 reported patients
- SplenomegalyHPOHP:0001744
- 7 of 7 reported patients
- ThrombocytopeniaHPOHP:0001873
- 7 of 7 reported patients
- Decreased total leukocyte countHPOHP:0001882
- 5 of 7 reported patients
Show the remaining 1
- Global developmental delayHPOHP:0001263
- 2 of 7 reported patients
Genes
1 gene
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.
- VPS45HGNC:14579
- Strong · Labcorp Genetics (formerly Invitae) · Autosomal recessive · 2021
- Strong · PanelApp Australia · Autosomal recessive · 2025
- Moderate · Natera · Autosomal recessive · 2023
- Supportive · Orphanet · Autosomal recessive · 2021
Where it sits
Other names
2 names
Resolves to: congenital neutropenia-myelofibrosis-nephromegaly syndrome
- Also called
- congenital neutropenia-bone marrow fibrosis-nephromegaly syndromevps45 deficiency