DiseaseID 4055
神经节神经瘤
disease
NCI2016_CDISC_1602D:A benign neoplasm characterized by the presence of ganglion cells and spindle cell proliferation, located primarily in the brain, ganglia, or adrenal medulla.|NCI2016_02D:A well differentiated, slow g
Relationship Network
Interactive first-hop connections across herbs, ingredients, formulas, targets, diseases, symptoms, syndromes, evidence, and monographs.
Click a node to open it in a new tab
Disease: 1Formula: 9Symptom: 11Target: 17Links: 44
Arranging relationship network...
Record Fields
Scalar fields from the final disease record.
- Disease Id
- 4055
- Core Entity Id
- 60343
- Source Entity Count
- 2
- Preferred Name
- Ganglioneuroma
- Name Cn
- 神经节神经瘤
- Name Pinyin
- Shen Jing Jie Shen Jing Liu
- Name En
- Ganglioneuroma
- Name Latin
- Bilingual Status
- complete
- Disease Type
- disease
- Umls Disease Type
- Neoplastic Process
- Disgenet Type
- disease
- Mesh Class
- Neoplasms
- Do Class
- disease of anatomical entity; disease of cellular proliferation
- Hpo Class
- Neoplasm; Abnormality of the nervous system
- Mesh Class Name
- Neoplasms
- Hpo Class Name
- Abnormality of the nervous system; Neoplasm
- Do Class Name
- disease of anatomical entity; disease of cellular proliferation
- Disease Definition
- NCI2016_CDISC_1602D:A benign neoplasm characterized by the presence of ganglion cells and spindle cell proliferation, located primarily in the brain, ganglia, or adrenal medulla.|NCI2016_02D:A well differentiated, slow growing neuroepithelial neoplasm composed of neoplastic, mature ganglion cells.|NCI2016_02D:A benign neuroblastic tumor of the sympathetic nervous system that occurs in childhood. Ganglioneuroma typically arises from the sympathetic trunk in the mediastinum. Histologic features include spindle cell proliferation (resembling a neurofibroma) and the presence of large ganglion cells. Common presenting features include a palpable abdominal mass, hepatomegaly, and a thoracic mass detected on routine chest X-ray.|MSH2017_2016_08_12:A benign neoplasm that usually arises from the sympathetic trunk in the mediastinum. Histologic features include spindle cell proliferation (resembling a neurofibroma) and the presence of large ganglion cells. The tumor may present clinically with HORNER SYNDROME or diarrhea due to ectopic production of vasoactive intestinal peptide. (From DeVita et al., Cancer: Principles and Practice of Oncology, 5th ed, p966)|HPO2016_07_04:A benign neoplasm that usually arises from the sympathetic trunk in the mediastinum, representing a tumor of the sympathetic nerve fibers arising from neural crest cells. [HPO:probinson]
- Version
- v2
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Ganglioneuroma
Role
preferred
Name
Gangliocytoma
Role
alias
Cross References
Trusted external identifiers retained for this final record.
Hpo
HP:0003005
Herb
HBDIS001125
Me Sh
D005729
Umls
C0017075
Sym Map
SMDE08911
Do Class
DOID:14566DOID:7
Dis Ge Net
C0017075
Umls Sty
T191
Hpo Class
HP:0000707HP:0000707;HP:0002664HP:0002664
Me Sh Class
C04
Etcm Disease
Ganglioneuroma
Tcmbank Disease
2222225251
Itcmdb Generated
ITX-DISEASE-20EC2C1968A0ITX-DISEASE-FCEF73666415
Attributes
Merged source attributes and domain-specific metadata.
Version
v2
Suppress
0
Page Title
Disease Ganglioneuroma Details page
Do Class Name
disease of anatomical entity; disease of cellular proliferation
Disease Type
disease
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
Basic Information
Disease Name
Ganglioneuroma
Global Category
Cancer diseases;Rare diseases
Anatomical Category
Neuronal diseases
Disease Definition
NCI2016_CDISC_1602D:A benign neoplasm characterized by the presence of ganglion cells and spindle cell proliferation, located primarily in the brain, ganglia, or adrenal medulla.|NCI2016_02D:A well differentiated, slow growing neuroepithelial neoplasm composed of neoplastic, mature ganglion cells.|NCI2016_02D:A benign neuroblastic tumor of the sympathetic nervous system that occurs in childhood. Ganglioneuroma typically arises from the sympathetic trunk in the mediastinum. Histologic features include spindle cell proliferation (resembling a neurofibroma) and the presence of large ganglion cells. Common presenting features include a palpable abdominal mass, hepatomegaly, and a thoracic mass detected on routine chest X-ray.|MSH2017_2016_08_12:A benign neoplasm that usually arises from the sympathetic trunk in the mediastinum. Histologic features include spindle cell proliferation (resembling a neurofibroma) and the presence of large ganglion cells. The tumor may present clinically with HORNER SYNDROME or diarrhea due to ectopic production of vasoactive intestinal peptide. (From DeVita et al., Cancer: Principles and Practice of Oncology, 5th ed, p966)|HPO2016_07_04:A benign neoplasm that usually arises from the sympathetic trunk in the mediastinum, representing a tumor of the sympathetic nerve fibers arising from neural crest cells. [HPO:probinson]
Me Sh Disease Class
Neoplasms
Dis Ge Net Disease Type
disease
Disease Class Name Me Sh
Neoplasms
Umls Semantic Type Name
Neoplastic Process