FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term Kindler syndrome ID (Ontology) DOID:0060472 (Human Disease)
Definition A skin disease characterized by congenital blistering, skin atrophy, photosensitivity, skin fragility, and scaling.
Also Known As "hereditary acrokeratotic poikiloderma of Kindler-Weary" ; "poikiloderma of Kindler"
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 Genes
 Kindler syndrome       2
 for disease ribbon | Kindler syndrome       2
 model of | Kindler syndrome       2
Spanning Tree (Parents/Children)
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  integumentary system disease
   |__skin disease
       |__Kindler syndrome  2 rec.
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Is a skin disease
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Synonyms
  • "hereditary acrokeratotic poikiloderma of Kindler-Weary" EXACT
    "poikiloderma of Kindler" EXACT
Secondary IDs
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GARD:4391
MESH:C536321
MIM:173650
ORDO:306539