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
Disease Subtypes
SHORT syndrome
Immunodeficiency 36 with lymphoproliferation

Rare disease

Projects

Including projects on subtypes.

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