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Pathways

Ontology Browser

Term:
Parent Terms Term With Siblings Child Terms
ABC Disease 
benign neoplasm +   
cancer +   
Chromosomal Instability with Tissue-Specific Radiosensitivity 
Cutaneous Telangiectasia and Cancer Syndrome, Familial  
Cysts +   
Experimental Neoplasms +   
Hamartoma +   
A focal malformation resembling a neoplasm, composed of an overgrowth of mature cells and tissues that normally occur in the affected area.
Hereditary Neoplastic Syndromes +   
Multiple Primary Neoplasms +   
Neoplasms by Histologic Type +   
Neoplasms by Site +   
Neoplasms, Hormone-Dependent  
Neoplasms, Post-Traumatic 
Neoplasms, Second Primary  
Neoplastic Pregnancy Complications +   
Neoplastic Processes +   
Paraneoplastic Syndromes +   
pre-malignant neoplasm +   
Radiation-Induced Neoplasms +   
Tumor Predisposition Syndrome +   
X-linked immunodeficiency with magnesium defect, Epstein-Barr virus infection, and neoplasia  

Synonyms
Exact Synonyms: Hamartomas
Narrow Synonyms: Chondroid Hamartoma ;   Colorectal Hamartoma ;   Gastrointestinal Hamartoma
Primary IDs: MESH:D006222
Xrefs: EFO:1000175 ;   EFO:1000193 ;   EFO:1000280 ;   EFO:1000634
Definition Sources: MESH:D006222

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