FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
Help Close All Open All
General Information
Term neurofibromatosis ID (Ontology) DOID:8712 (Human Disease)
Definition
Comment
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      64
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
 neurofibromatosis      66     30
 ameliorates | neurofibromatosis      46       --
 exacerbates | neurofibromatosis       9       --
 model of | neurofibromatosis      10       --
 DOES NOT ameliorate | neurofibromatosis       1       --
Spanning Tree (Parents/Children)
Only view relationship: 
autosomal genetic disease
 |__autosomal dominant disease__
syndrome                        |
 |__RASopathy___________________|
                                neurofibromatosis  100 rec.
                                 |__neurofibromatosis 1 16 rec.
                                     |__spinal neurofibromatosis 1 rec.
Spanning Tree View Settings
Parents/Children
View Depth
Show hierarchy levels: for parents, for children
hide Relationships
Is a autosomal dominant disease
RASopathy
Part of
hide Synonyms & Secondary IDs
Synonyms
Secondary IDs
hide External Crossreferences & Linkouts
GARD:10420
ICD10CM:Q85.0
ICD9CM:237.7
MESH:D017253
NCI:C6727
ORDO:634518
SNOMEDCT_US_2023_03_01:19133005
UMLS_CUI:C0162678
UMLS_CUI:C0495632