FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term cystic fibrosis ID (Ontology) DOID:1485 (Human Disease)
Definition A syndrome that is characterized by the buildup of thick, sticky mucus that can damage many organs.
Also Known As "CF" ; "mucoviscidosis"
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Links to External Ontologies
DO.org
Annotations
Records annotated with this term OR any of its CHILD TERMS
Records annotated with this exact term (annotations to child terms are NOT included)
Data Class Field Records
Alleles (FBal)  HUMAN_DISEASE_INTERACTIONS      17
Human Disease Models (FBhh)  DOID       2
show Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
 Full annotation statements 
Relevant FlyBase reports
 Alleles Genes Human Disease Models
 cystic fibrosis      17      9      2
 ameliorates | cystic fibrosis       4       --       --
 for disease ribbon | cystic fibrosis       --       6       --
 model of | cystic fibrosis      13      6       --
Spanning Tree (Parents/Children)
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autosomal genetic disease
 |__autosomal recessive disease__
disease                          |
 |__syndrome_____________________|
                                 cystic fibrosis  28 rec.
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Is a autosomal recessive disease
syndrome
Part of
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Synonyms
  • "CF" EXACT OMO:0003012
    "mucoviscidosis" EXACT
Secondary IDs
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GARD:6233
ICD10CM:E84
ICD9CM:277.0
MESH:D003550
MIM:219700
NCI:C2975
ORDO:586
SNOMEDCT_US_2023_03_01:85809002
UMLS_CUI:C0010674