FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
Help Close All Open All
General Information
Term pigmentation disease ID (Ontology) DOID:10123 (Human Disease)
Definition A skin disease that is characterized by discoloration of the skin.
Comment
Links to External Ontologies
DO.org
Annotations
Records annotated with this term OR any of its CHILD TERMS
    Results list data from multiple species. Click on a button above and use the 'Filter by species' options on the resulting HitList to retrieve species-specific data.
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:
  integumentary system disease
   |__skin disease
       |__pigmentation disease  10 rec.
           |__acanthosis nigricans
           |__Bloch-Sulzberger syndrome
           |__conjunctival pigmentation
           |__Dowling-Degos disease 3 rec.
           |__dyschromatosis symmetrica hereditaria 2 rec.
           |__dyschromatosis universalis hereditaria 2 rec.
           |__hyperpigmentation of eyelid
           |__hypopigmentation of eyelid
           |__neonatal jaundice
           |   |__kernicterus due to isoimmunization
           |   |__perinatal jaundice due to hepatocellular damage
           |__reticulate acropigmentation of Kitamura 2 rec.
           |__stromal corneal pigmentation
           |__X-linked reticulate pigmentary disorder 1 rec.
Spanning Tree View Settings
Parents/Children
View Depth
Show hierarchy levels: for parents, for children
hide Relationships
Is a skin disease
Part of
hide Synonyms & Secondary IDs
Synonyms
Secondary IDs
hide External Crossreferences & Linkouts
ICD9CM:709.09
UMLS_CUI:C0375489