Adult Adamantinomatous Craniopharyngioma

Preferred Label : Adult Adamantinomatous Craniopharyngioma;

NCIt definition : An adamantinomatous craniopharyngioma that occurs in adults.;

Neoplastic status : Benign;

NCI Metathesaurus CUI : CL1794008;

Details

Origin ID

C188949;

UMLS CUI

C5708144;

Disease excludes abnormal cell
- Malignant Cell [NCIt concept]
- Malignant Epithelial Cell [NCIt concept]
- Malignant Squamous Cell [NCIt concept]
- Neoplastic Glandular Cell [NCIt concept]
- Neoplastic Smooth Muscle Cell [NCIt concept]
Disease excludes normal cell origin
- Endocrine-Stromal Cell [NCIt concept]
Disease may have findings
- Visual Disturbance [NCIt concept]
Excludes anatomical site(s)
- Spinal Cord [NCIt concept]
Has associated anatomic sites
- Base of the Skull [NCIt concept]
- Brain [NCIt concept]
- Central Nervous System [NCIt concept]
- Head and Neck [NCIt concept]
- Nervous System [NCIt concept]
- Sellar Region [NCIt concept]
- Skull [NCIt concept]
Semantic type(s)
- Neoplastic Process [UMLS semantic type]
disease_excludes_finding
- Borderline Lesion [NCIt concept]
- Malignant Cellular Infiltrate [NCIt concept]
- Mixed Cellular Population [NCIt concept]
- Mixed Neoplastic Glandular and Squamous Cell Population [NCIt concept]
- Pseudopapillary Pattern [NCIt concept]
disease_has_abnormal_cell
- Neoplastic Cell [NCIt concept]
- Neoplastic Epithelial Cell [NCIt concept]
- Neoplastic Squamous Cell [NCIt concept]
disease_has_finding
- Adulthood Lesion [NCIt concept]
- Benign Cellular Infiltrate [NCIt concept]
- Cholesterol Deposit [NCIt concept]
- Cystic Lesion [NCIt concept]
- Dystrophic Calcification [NCIt concept]
- Epithelial Component Present [NCIt concept]
- Nodules of Compact Keratin Present [NCIt concept]
- Nuclear Palisading [NCIt concept]
- Rare Lesion [NCIt concept]
- Slow Growing Mass [NCIt concept]
disease_has_grade
- Grade 1 [NCIt concept]
disease_has_normal_cell_origin
- Epithelial Cell [NCIt concept]
disease_has_normal_tissue_origin
- Epithelial Tissue [NCIt concept]
- Rathke Pouch Epithelium [NCIt concept]
disease_has_primary_anatomic_site
- Base of the Skull [NCIt concept]
- Brain [NCIt concept]
- Central Nervous System [NCIt concept]
- Head [NCIt concept]
- Head and Neck [NCIt concept]
- Nervous System [NCIt concept]
- Sellar Region [NCIt concept]
- Skull [NCIt concept]
disease_mapped_to_gene
- CTNNB1 Gene [NCIt concept]
disease_may_have_associated_disease
- Endocrine System Disorder [NCIt concept]
disease_may_have_molecular_abnormality
- CTNNB1 Gene Mutation [NCIt concept]

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