Histology
Hereditary Benign Intraepithelial Dyskeratosis
CI-CAN-00002860HBIDExplore in graph →
Non-malignant
- NCIt
- C3940
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Histology
CI-CAN-00002860HBIDExplore in graph →
Data completeness0 / 7 dimensions
Computed from entity_counters.completeness · refreshed after each connector run
Definition
A rare autosomal dominant disorder with high penetrance that affects the limbal conjunctiva or oral mucosa. It is almost exclusively encountered in Native Americans belonging to the Haliwa-Saponi tribe of northeastern North Carolina and is caused by a duplication in chromosome 4q35. It is characterized by the presence of elevated epithelial dyskeratotic plaques in the limbal conjunctiva or oral cavity. Epithelial dysplasia is absent.
Data updated 22 days agoSource updated 26.08e
Taxonomy
Several hierarchies coexist; edges are listed per hierarchy type with their source.
Anatomy
Data not yet available
Data updated 3 hours agoSource updated unknowncounters aggregate over descendants
Names
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Key figures
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No registry-level ancestor: burden figures are published for the mutually exclusive top-level site groups only, and this entity does not descend from one. Global figures (IARC / GLOBOCAN) stay under license review and SEER awaits credentials.
Data updated 3 hours agoSource updated unknownregistry figures: none · counters aggregate over descendants