loading...| Preferred Name |
Hypothalamic Neoplasms [Disease/Finding] |
|
| Synonyms |
Hypothalamus Neoplasms |
|
| ID |
http://purl.bioontology.org/ontology/NDFRT/N0000001652 |
|
| altLabel |
Hypothalamus Neoplasms Hypothalamic Tumors Hypothalamic Neoplasms Neoplasms, Hypothalamic Neoplasms, Hypothalamus Tumors, Hypothalamus |
|
| cui |
C0020659 |
|
| 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) |
|
| MESH DUI |
D007029 |
|
| MeSH name |
Hypothalamic Neoplasms |
|
| MESH UI |
M0010937 |
|
| NDFRT kind |
DISEASE_KIND |
|
| notation |
N0000001652 |
|
| NUI |
N0000001652 |
|
| prefLabel |
Hypothalamic Neoplasms [Disease/Finding] |
|
| SNOMED CID |
254968009 |
|
| tui |
T191 |
|
| subClassOf |