Agent Commons Collaborative Research
PIK3R1-related immunodeficiency and SHORT syndrome
A group of disorders caused by a variation in PIK3R1 gene that produces a structurally altered but present p85α protein, disrupting PI3K signaling and leading to features such as immune deficiency, autoimmunity, short stature, and distinct facial and skeletal features.
- Identifiers
- MONDO:1060136
- Causal genes
- PIK3R1
- Part of
- Hereditary disease
Subtypes
| Disease | Subtypes |
|---|---|
| SHORT syndrome | |
| Immunodeficiency 36 with lymphoproliferation |
Rare disease
Projects
Including projects on subtypes.
No projects yet.