neutropenia, severe congenital, 12, autosomal recessive
MONDO:0980936Mondo
Findings
No curated finding names neutropenia, severe congenital, 12, autosomal recessive 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
47 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.
- Atopic dermatitisHPOHP:0001047
- 2 of 2 reported patients
- Autoimmune hemolytic anemiaHPOHP:0001890
- 1 of 1 reported patient
- Bone marrow hypocellularityHPOHP:0005528
- 1 of 1 reported patient
- BronchitisHPOHP:0012387
- 1 of 1 reported patient
- CellulitisHPOHP:0100658
- 1 of 1 reported patient
- Decreased mean corpuscular hemoglobin concentrationHPOHP:0025547
- 1 of 1 reported patient
- Decreased mean corpuscular volumeHPOHP:0025066
- 1 of 1 reported patient
- Decreased total lymphocyte countHPOHP:0001888
- 3 of 3 reported patients
- Decreased total neutrophil countHPOHP:0001875
- 3 of 3 reported patients
- Decreased total T cell countHPOHP:0005403
- 2 of 2 reported patients
- EnterocolitisHPOHP:0004387
- 1 of 1 reported patient
- Equinovarus deformityHPOHP:0008110
- 1 of 1 reported patient
Show the remaining 35
- FuruncleHPOHP:0020083
- 1 of 1 reported patient
- HepatosplenomegalyHPOHP:0001433
- 1 of 1 reported patient
- Increased total monocyte countHPOHP:0012311
- 1 of 1 reported patient
- MeningitisHPOHP:0001287
- 1 of 1 reported patient
- MyopiaHPOHP:0000545
- 1 of 1 reported patient
- OsteomyelitisHPOHP:0002754
- 1 of 1 reported patient
Where it sits
- A kind of