FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
Help Close All Open All
General Information
Term autoimmune polyendocrine syndrome type 2 ID (Ontology) DOID:0050168 (Human Disease)
Definition An autoimmune polyendocrine syndrome that is characterized by abnormal functioning of the immune system that causes auto-reactivity against endocrine organs. It is more heterogeneous and has not been linked to one gene." [url:http\://en.wikipedia.org/wiki/Autoimmune_polyendocrine_syndrome_type_2] {comment="sn:IEDB"}
Also Known As "Schmidt syndrome"
Comment
Links to External Ontologies
DO.org
Annotations
Records annotated with this term OR any of its CHILD TERMS
No relevant records available
Records annotated with this exact term (annotations to child terms are NOT included)
No relevant records available
show Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
No relevant statements available
Spanning Tree (Parents/Children)
Only view relationship:
  autoimmune disease of endocrine system
   |__autoimmune polyendocrine syndrome
       |__autoimmune polyendocrine syndrome type 2
Spanning Tree View Settings
Parents/Children
View Depth
Show hierarchy levels: for parents, for children
hide Relationships
Is a autoimmune polyendocrine syndrome
Part of
hide Synonyms & Secondary IDs
Synonyms
  • "Schmidt syndrome" EXACT
Secondary IDs
hide External Crossreferences & Linkouts
GARD:7611
MIM:269200