reticular dysgenesis
ICD-10: D81.0MeSH: C538361ORPHA: 33355
Overview
Human disease
Available Treatments (0)
No treatments linked yet
Clinical trials or compassionate use may be available — consult a specialist.
Clinical Presentation
Signs and symptoms associated with reticular dysgenesis, sourced from HPO and Orphanet clinical annotations.
Hearing impairmentChronic otitis mediaSkin rashFailure to thriveWeight lossAbnormality of neutrophilsDecreased total leukocyte countAnemiaDehydrationFeverDiarrheaMalabsorptionRecurrent respiratory infectionsAbnormality of mitochondrial metabolismDecreased circulating immunoglobulin concentrationSevere combined immunodeficiencyCellular immunodeficiencyAplasia/Hypoplasia of the thymusSepsisSkin ulcerLymphopenia
Classification & Codes
ICD-10 Code
D81.0MeSH Code
C538361Orphanet Code
ORPHA:33355reticular dysgenesis
| ICD-10 | D81.0 |
| MeSH | C538361 |
| Orphanet | ORPHA:33355 |
| Treatments | 0 drug(s) |
| Symptoms on record | 21 signs |
| Status | published |
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO