FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
Help Close All Open All
General Information
Term congenital stationary night blindness ID (Ontology) DOID:0050534 (Human Disease)
Definition A hereditary night blindness that is characterized by hemeralopia with a moderate loss of visual acuity and caused by defective photoreceptor-to-bipolar cell signaling with common ERG findings of reduced or absent b-waves and generally normal a-waves.
Also Known As "congenital essential nyctalopia"
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
Human Disease Models (FBhh)  DOID       1
show Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
 Full annotation statements 
Relevant FlyBase reports
 Human Disease Models
 congenital stationary night blindness       1
Spanning Tree (Parents/Children)
Only view relationship: 
disease
 |__physical disorder___________
night blindness                 |
 |__hereditary night blindness__|
                                congenital stationary night blindness  23 rec.
                                 |__congenital stationary night blindness 1A 2 rec.
                                 |__congenital stationary night blindness 1B 4 rec.
                                 |__congenital stationary night blindness 1C 1 rec.
                                 |__congenital stationary night blindness 1D 1 rec.
                                 |__congenital stationary night blindness 1E 3 rec.
                                 |__congenital stationary night blindness 1F 1 rec.
                                 |__congenital stationary night blindness 1G 1 rec.
                                 |__congenital stationary night blindness 1H 2 rec.
                                 |__congenital stationary night blindness 2A 1 rec.
                                 |__congenital stationary night blindness autosomal dominant 1
                                 |__congenital stationary night blindness autosomal dominant 2 1 rec.
                                 |__congenital stationary night blindness autosomal dominant 3 1 rec.
                                 |__Oguchi disease-1 4 rec.
                                 |__Oguchi disease-2 1 rec.
Spanning Tree View Settings
Parents/Children
View Depth
Show hierarchy levels: for parents, for children
hide Relationships
Is a physical disorder
hereditary night blindness
Part of
hide Synonyms & Secondary IDs
Synonyms
  • "congenital essential nyctalopia" EXACT
Secondary IDs
hide External Crossreferences & Linkouts
ICD10CM:H53.63
ICD9CM:368.61
MESH:C537743
MIM:PS310500
ORDO:215
SNOMEDCT_US_2023_03_01:193687000
UMLS_CUI:C1306122