loading...| Preferred Name |
Hemangioblastoma |
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| Synonyms |
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| Definitions |
A WHO grade I tumor of uncertain histogenesis which is composed of stromal cells and abundant capillaries. Approximately 25% of hemangioblastomas are associated with Von Hippel-Lindau disease, a disease inherited through an autosomal dominant trait and characterized by the development of hemangioblastomas of the central nervous system and retina, clear cell renal carcinoma, pheochromocytoma, and pancreatic and inner ear tumors. (Adapted from WHO) |
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| ID |
http://purl.obolibrary.org/obo/NCIT_C3801 |
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| code |
C3801 |
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| Contributing_Source |
GDC |
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| definition |
A WHO grade I tumor of uncertain histogenesis which is composed of stromal cells and abundant capillaries. Approximately 25% of hemangioblastomas are associated with Von Hippel-Lindau disease, a disease inherited through an autosomal dominant trait and characterized by the development of hemangioblastomas of the central nervous system and retina, clear cell renal carcinoma, pheochromocytoma, and pancreatic and inner ear tumors. (Adapted from WHO) |
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| ICD-O-3_Code |
9161/1 |
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| in_subset |
http://purl.obolibrary.org/obo/NCIT_C168658 http://purl.obolibrary.org/obo/NCIT_C168656 http://purl.obolibrary.org/obo/NCIT_C168657 http://purl.obolibrary.org/obo/NCIT_C168655 http://purl.obolibrary.org/obo/NCIT_C168662 http://purl.obolibrary.org/obo/NCIT_C168661 http://purl.obolibrary.org/obo/NCIT_C177537 http://purl.obolibrary.org/obo/ncit#oncotree_slim |
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| Is_Value_For_GDC_Property | ||
| label |
Hemangioblastoma |
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| Legacy Concept Name |
Hemangioblastoma |
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| Maps_To |
Hemangioblastoma Angioblastoma Haemangioblastoma 9161/1 |
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| Neoplastic_Status |
Undetermined |
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| Preferred_Name |
Hemangioblastoma |
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| prefixIRI |
NCIT:C3801 |
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| prefLabel |
Hemangioblastoma |
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| Semantic_Type |
Neoplastic Process |
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| UMLS_CUI |
C0206734 |
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| subClassOf |