Preferred Name |
Hypothalamic Neoplasms [Disease/Finding] |
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Synonyms |
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ID |
http://evs.nci.nih.gov/ftp1/NDF-RT/NDF-RT.owl#N0000001652 |
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code |
C3482 |
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Display_Name |
Hypothalamic Neoplasms |
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imported from | ||
label |
Hypothalamic Neoplasms [Disease/Finding] |
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MeSH_CUI |
M0010937 |
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MeSH_Definition |
Benign and malignant tumors of the HYPOTHALAMUS. Pilocytic astrocytomas and hamartomas are relatively frequent histologic types. Neoplasms of the hypothalamus frequently originate from adjacent structures, including the OPTIC CHIASM, optic nerve (see OPTIC NERVE NEOPLASMS), and pituitary gland (see PITUITARY NEOPLASMS). Relatively frequent clinical manifestations include visual loss, developmental delay, macrocephaly, and precocious puberty. (From Devita et al., Cancer: Principles and Practice of Oncology, 5th ed, p2051) |
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MeSH_DUI |
D007029 |
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MeSH_Name |
Hypothalamic Neoplasms |
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NUI |
N0000001652 |
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prefixIRI |
NDF-RT:N0000001652 |
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prefLabel |
Hypothalamic Neoplasms [Disease/Finding] |
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RxNorm_CUI |
1021928 |
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SNOMED_CID |
254968009 |
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Synonym |
Hypothalamic Tumors Tumors, Hypothalamus Neoplasms, Hypothalamic Hypothalamus Neoplasms Neoplasms, Hypothalamus |
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UMLS_CUI |
C0020659 |
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subClassOf |
Delete | Mapping To | Ontology | Source |
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http://purl.bioontology.org/ontology/NDFRT/N0000001652 | NDFRT | LOOM |