autosomal recessive severe congenital neutropenia due to JAGN1 deficiency
MONDO:0014456Mondo
Findings
No curated finding names autosomal recessive severe congenital neutropenia due to JAGN1 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
HPO, annotations 2026-09-02
Features
7 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
- 12 of 12 reported patients
- Bone marrow maturation arrestHPOHP:0033606
- 13 of 14 reported patients
- Short statureHPOHP:0004322
- 2 of 14 reported patients
- Failure to thriveHPOHP:0001508
- 1 of 14 reported patients
- Recurrent bacterial infectionsHPOHP:0002718
- Recurrent otitis mediaHPOHP:0000403
- Recurrent respiratory infectionsHPOHP:0002205
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.
- JAGN1HGNC:26926
- Definitive · G2P · Autosomal recessive · 2015
- Strong · Labcorp Genetics (formerly Invitae) · Autosomal recessive · 2023
- Strong · PanelApp Australia · Autosomal recessive · 2025
- Supportive · Orphanet · Autosomal recessive · 2021