neutropenia, severe congenital, 11, autosomal dominant
MONDO:0958017Mondo
Findings
No curated finding names neutropenia, severe congenital, 11, autosomal dominant yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
- Inheritance
- Autosomal dominant inheritance
- Onset and course
- Infantile onset
HPO, annotations 2026-09-02
Features
23 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
- 1 of 1 reported patient
- Aphthous ulcerHPOHP:0032154
- 1 of 1 reported patient
- Bone marrow maturation arrestHPOHP:0033606
- 1 of 1 reported patient
- Decreased total neutrophil countHPOHP:0001875
- 1 of 1 reported patient
- GingivitisHPOHP:0000230
- 1 of 1 reported patient
- HyperuricemiaHPOHP:0002149
- 1 of 1 reported patient
- Increased circulating IgA concentrationHPOHP:0003261
- 1 of 1 reported patient
- Increased circulating IgG2 concentrationHPOHP:0032299
- 1 of 1 reported patient
- Increased plasmablast proportionHPOHP:0032128
- 1 of 1 reported patient
- Increased total monocyte countHPOHP:0012311
- 1 of 1 reported patient
- Perianal abscessHPOHP:0009789
- 1 of 1 reported patient
- Pleural empyemaHPOHP:0011919
- 1 of 1 reported patient
Show the remaining 11
- PneumoniaHPOHP:0002090
- 1 of 1 reported patient
- Poor wound healingHPOHP:0001058
- 1 of 1 reported patient
- Recurrent aphthous stomatitisHPOHP:0011107
- 1 of 1 reported patient
- Recurrent gingivitisHPOHP:0034284
- 1 of 1 reported patient
- Recurrent otitis mediaHPOHP:0000403
- 1 of 1 reported patient
- Recurrent sinusitisHPOHP:0011108
- 1 of 1 reported patient
Where it sits
- A kind of