Colorectal Benign Granular Cell Tumor

Preferred Label : Colorectal Benign Granular Cell Tumor;

NCIt definition : A granular cell tumor that arises from the colon or rectum and is characterized by the absence of atypical or malignant cytological and architectural features, and absence of invasive features or metastatic potential.;

Neoplastic status : Undetermined;

Details

Origin ID

C96516;

UMLS CUI

C3272838;

Disease excludes abnormal cell
- Malignant Cell [NCIt concept]
- Malignant Polygonal Cell with Abundant Granular Cytoplasm [NCIt concept]
Has associated anatomic sites
- Colorectal Region [NCIt concept]
- Digestive System [NCIt concept]
- Intestine [NCIt concept]
- Nervous System [NCIt concept]
Semantic type(s)
- Neoplastic Process [UMLS semantic type]
disease_excludes_finding
- Malignant Cellular Infiltrate [NCIt concept]
disease_excludes_normal_tissue_origin
- Lymphoid Tissue [NCIt concept]
disease_has_abnormal_cell
- Neoplastic Cell [NCIt concept]
- Neoplastic Neuroepithelial Cell and Neoplastic Perineural Cell [NCIt concept]
- Neoplastic Perineural Cell [NCIt concept]
- Neoplastic Polygonal Cell with Abundant Granular Cytoplasm [NCIt concept]
disease_has_finding
- Benign Cellular Infiltrate [NCIt concept]
disease_has_normal_cell_origin
- Neuron, Neuroepithelial Cell, and Supporting Cell of the Nervous System [NCIt concept]
- Perineural Cell [NCIt concept]
disease_has_normal_tissue_origin
- Nerve Tissue and Nerve Sheaths [NCIt concept]
- Nerve Tissue, Neuroepithelial Tissue, and Nerve Sheaths [NCIt concept]
disease_has_primary_anatomic_site
- Colorectal Region [NCIt concept]
- Digestive System [NCIt concept]
- Large Intestine [NCIt concept]
- Nervous System [NCIt concept]
disease_mapped_to_gene
- ATP6AP1 Gene [NCIt concept]
- ATP6AP2 Gene [NCIt concept]
disease_may_have_molecular_abnormality
- ATP6AP1 Gene Mutation [NCIt concept]
- ATP6AP2 Gene Mutation [NCIt concept]

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