DiseaseID 4912

松果体细胞瘤

disease

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Disease: 1Symptom: 12Target: 12Links: 24

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Record Fields

Scalar fields from the final disease record.

Disease Id: 4912
Core Entity Id: 61333
Source Entity Count: 1
Preferred Name: Pineocytoma
Name Cn: 松果体细胞瘤
Name Pinyin: Song Guo Ti Xi Bao Liu
Name En: Pineocytoma
Name Latin
Bilingual Status: complete
Disease Type: disease
Umls Disease Type: Neoplastic Process
Disgenet Type: disease
Mesh Class: Nervous System Diseases; Neoplasms
Do Class: disease of anatomical entity; disease of cellular proliferation
Hpo Class: Neoplasm; Abnormality of the nervous system
Mesh Class Name: Neoplasms; Nervous System Diseases
Hpo Class Name: Abnormality of the nervous system; Neoplasm
Do Class Name: disease of anatomical entity; disease of cellular proliferation
Disease Definition: NCI2016_02D:A benign or malignant neoplasm that occurs within the intracranial cavity above the tentorium cerebelli.|MSH2017_2016_08_12:Primary and metastatic (secondary) tumors of the brain located above the tentorium cerebelli, a fold of dura mater separating the CEREBELLUM and BRAIN STEM from the cerebral hemispheres and DIENCEPHALON (i.e., THALAMUS and HYPOTHALAMUS and related structures). In adults, primary neoplasms tend to arise in the supratentorial compartment, whereas in children they occur more frequently in the infratentorial space. Clinical manifestations vary with the location of the lesion, but SEIZURES; APHASIA; HEMIANOPSIA; hemiparesis; and sensory deficits are relatively common features. Metastatic supratentorial neoplasms are frequently multiple at the time of presentation.|HPO2016_07_04:A benign or malignant neoplasm that occurs within the intracranial cavity above the tentorium cerebelli. []
Version: v2
Suppressed: No

Names

Preferred names, aliases, and source labels retained in the final schema.

Name

Pineocytoma

Role

preferred

Name

Pineal Gland Neoplasm

Role

preferred

Name

Pineoblastoma

Role

preferred

Name

Supratentorial Neoplasms

Role

preferred

Name

Tumor Of The Pineal Region

Role

preferred

Name

Benign Supratentorial Neoplasms

Role

preferred

Name

Cancer, Supratentorial

Role

preferred

Name

Pineal Parenchymal Tumor of Intermediate Differentiation

Role

preferred

Name

Primary Supratentorial Neoplasms

Role

preferred

Name

Pineal Gland Cancer

Role

alias

Name

Pineal Parenchymal Cell Neoplasm

Role

alias

Name

Pineal Parenchymal Tumor

Role

alias

Name

Pineal Parenchymal Tumour

Role

alias

Name

Pinealoblastoma

Role

alias

Name

Pinealoma

Role

alias

Name

Supratentorial Cancer

Role

alias

Name

Supratentorial Neoplasm

Role

alias

Cross References

Trusted external identifiers retained for this final record.

Hpo

HP:0010799HP:0030407HP:0030408HP:0030693HP:0030694

Herb

HBDIS002395HBDIS002882HBDIS004317HBDIS011372HBDIS011373HBDIS011374HBDIS012381HBDIS014032HBDIS014209

Me Sh

D010871D015173

Umls

C0031941C0038874C0205898C0917890C1412004

Sym Map

SMDE12172SMDE12173SMDE12174SMDE13744SMDE14052

Do Class

DOID:14566DOID:7

Dis Ge Net

C0031941C0038874C0205898C0751588C0751589C0751590C0917890C1367859C1412004

Umls Sty

T191

Hpo Class

HP:0000707HP:0002664

Me Sh Class

C04C10

Tcmbank Disease

1019315816182322697230262607520970777082

Itcmdb Generated

ITX-DISEASE-481524994118ITX-DISEASE-619D7CC580ECITX-DISEASE-9EDA745D5AA3ITX-DISEASE-B8B1E48D3D35ITX-DISEASE-F0E2E2CEAB95

Attributes

Merged source attributes and domain-specific metadata.

Version

Suppress

Do Class Name

disease of anatomical entity; disease of cellular proliferation

Disease Type

diseasegroup

Hpo Class Name

Abnormality of the nervous system; Neoplasm

Do Disease Class

disease of anatomical entity; disease of cellular proliferation

Hpo Disease Class

Neoplasm; Abnormality of the nervous system

Umls Disease Type

Neoplastic Process

Disease Definition

NCI2016_02D:A benign or malignant neoplasm that occurs within the intracranial cavity above the tentorium cerebelli.|MSH2017_2016_08_12:Primary and metastatic (secondary) tumors of the brain located above the tentorium cerebelli, a fold of dura mater separating the CEREBELLUM and BRAIN STEM from the cerebral hemispheres and DIENCEPHALON (i.e., THALAMUS and HYPOTHALAMUS and related structures). In adults, primary neoplasms tend to arise in the supratentorial compartment, whereas in children they occur more frequently in the infratentorial space. Clinical manifestations vary with the location of the lesion, but SEIZURES; APHASIA; HEMIANOPSIA; hemiparesis; and sensory deficits are relatively common features. Metastatic supratentorial neoplasms are frequently multiple at the time of presentation.|HPO2016_07_04:A benign or malignant neoplasm that occurs within the intracranial cavity above the tentorium cerebelli. []NCI2016_02D:A neoplasm arising from the pineocyte, a cell with photosensory and neuroendocrine functions. It may be composed of mature elements or primitive, immature cells. The cellular composition determines the biological behavior and clinical outcome. Three types are recognized: pineoblastoma, pineocytoma, and pineal parenchymal tumor of intermediate differentiation (Adapted from WHO.)|MSH2017_2016_08_12:Neoplasms which originate from pineal parenchymal cells that tend to enlarge the gland and be locally invasive. The two major forms are pineocytoma and the more malignant pineoblastoma. Pineocytomas have moderate cellularity and tend to form rosette patterns. Pineoblastomas are highly cellular tumors containing small, poorly differentiated cells. These tumors occasionally seed the neuroaxis or cause obstructive HYDROCEPHALUS or Parinaud's syndrome. GERMINOMA; CARCINOMA, EMBRYONAL; GLIOMA; and other neoplasms may arise in the pineal region with germinoma being the most common pineal region tumor. (From DeVita et al., Cancer: Principles and Practice of Oncology, 5th ed, p2064; Adams et al., Principles of Neurology, 6th ed, p670)|HPO2016_07_04:A neoplasm of the pineal gland. [HPO:probinson]|CSP2006:new abnormal pineal body tissue that grows by excessive cellular division and proliferation more rapidly than normal and continues to grow after the stimuli that initiated the new growth cease.NCI2016_NCI-GLOSS_1602D:A fast growing type of brain tumor that occurs in or around the pineal gland, a tiny organ near the center of the brain.|NCI2016_CDISC_1602D:A poorly differentiated malignant embryonal neoplasm arising from the pineal region of the brain.|NCI2016_02D:A poorly differentiated malignant embryonal neoplasm arising from the pineal region. It usually occurs in children and it is characterized by the presence of small immature neuroepithelial cells. It may follow an aggressive clinical course.|HPO2016_07_04:Pineoblastoma is a rare primitive neuroectodermal tumour (PNET) arising in the pineal gland. Pineoblastomas are classified as a WHO grade IV tumour and comprise one-fourth to one-half of pineal parenchymal tumours. Pineoblastoma is a highly cellular tumor originating in the pineal gland and containing small, poorly differentiated cells. [HPO:probinson] {comment="PMID:21717450"}NCI2016_NCI-GLOSS_1602D:A slow growing type of brain tumor that occurs in or around the pineal gland, a tiny organ near the center of the brain.|NCI2016_CDISC_1602D:A benign neoplasm of the brain arising from the pineal gland.|NCI2016_02D:A WHO grade I slow growing tumor, more frequently affecting young adults. It is composed of small, uniform, mature cells resembling pineocytes with occasional large pineocytomatous rosettes. It may show a wide range of divergent phenotypes, including neuronal, glial, melanocytic, photoreceptor and mesenchymal differentiation. Pineocytoma generally has a relatively favorable prognosis. (Adapted from WHO)|HPO2016_07_04:A type of pineal parenchymal cell neoplasm that is a mature well-differentiated tumour (WHO grade I). []NCI2016_NCI-GLOSS_1602D:A type of brain tumor that occurs in or around the pineal gland, a tiny organ near the center of the brain.|NCI2016_02D:Neoplasms that are located in the pineal gland. These neoplasms arise either from pineal parenchymal cells (pineocytes), as do pineocytomas and the more aggressive pineoblastomas, or from other cell types, as do pineal astrocytic tumors (notably pilocytic astrocytomas) and germ cell tumors. Clinical symptoms include neuro-ophthalmologic dysfunction, changes in mental status, dysfunction of the brain stem, and hypothalamic-based endocrine abnormalities.

Me Sh Disease Class

Nervous System Diseases; Neoplasms

Dis Ge Net Disease Type

diseasegroup

Disease Class Name Me Sh

Neoplasms; Nervous System Diseases

Umls Semantic Type Name

Neoplastic Process