DiseaseID 3567

副神经节瘤

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: 3567
Core Entity Id: 59788
Source Entity Count: 1
Preferred Name: Paraganglioma
Name Cn: 副神经节瘤
Name Pinyin: Fu Shen Jing Jie Liu
Name En: Paraganglioma
Name Latin
Bilingual Status: complete
Disease Type: disease
Umls Disease Type: Disease or Syndrome
Disgenet Type: disease
Mesh Class: Congenital, Hereditary, and Neonatal Diseases and Abnormalities; NeoplasmsNeoplasmsNervous System Diseases; Otorhinolaryngologic Diseases; Neoplasms; Pathological Conditions, Signs and Symptoms
Do Class: disease of anatomical entity; genetic disease; disease of cellular proliferation
Hpo Class: Neoplasm; Abnormality of the nervous system; Abnormality of the endocrine system
Mesh Class Name: Congenital, Hereditary, and Neonatal Diseases and Abnormalities; NeoplasmsNeoplasmsPathological Conditions, Signs and Symptoms; Neoplasms; Nervous System Diseases; Otorhinolaryngologic Diseases
Hpo Class Name: Abnormality of the endocrine system; Abnormality of the nervous system; Neoplasm
Do Class Name: genetic disease; disease of anatomical entity; disease of cellular proliferation
Disease Definition: NCI2016_02D:A benign or malignant extra-adrenal parasympathetic paraganglioma arising from paraganglia in the base of the skull and middle ear.|MSH2017_2016_08_12:A paraganglioma involving the glomus jugulare, a microscopic collection of chemoreceptor tissue in the adventitia of the bulb of the jugular vein. It may cause paralysis of the vocal cords, attacks of dizziness, blackouts, and nystagmus. It is not resectable but radiation therapy is effective. It regresses slowly, but permanent control is regularly achieved. (From Dorland, 27th ed; Stedman, 25th ed; DeVita Jr et al., Cancer: Principles & Practice of Oncology, 3d ed, pp1603-4)
Version: v1
Suppressed: No

Names

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

Name

Paraganglioma

Role

preferred

Name

Extra-Adrenal Paraganglioma

Role

preferred

Name

Paragangliomas 1

Role

preferred

Name

Paragangliomas 3

Role

preferred

Name

Paragangliomas 4

Role

preferred

Name

Paragangliomas 5

Role

preferred

Name

Paragangliomas With Sensorineural Hearing Loss

Role

preferred

Name

Carotid Body Paraganglioma

Role

preferred

Name

Glomus Jugulare Tumor

Role

preferred

Name

PARAGANGLIOMAS 1 WITH SENSORINEURAL HEARING LOSS

Role

preferred

Name

PARAGANGLIOMAS 2 (disorder)

Role

preferred

Name

CAROTID BODY TUMORS

Role

alias

Name

CAROTID BODY TUMORS AND MULTIPLE EXTRAADRENAL PHEOCHROMOCYTOMAS

Role

alias

Name

CBT1

Role

alias

Name

CHEMODECTOMAS

Role

alias

Name

Carotid Body Tumor

Role

alias

Name

Chemodectoma

Role

alias

Name

GLOMUS JUGULARE TUMORS

Role

alias

Name

GLOMUS TUMORS, FAMILIAL, 1

Role

alias

Name

GLOMUS TUMORS, FAMILIAL, 3

Role

alias

Name

Glomus Jugular Tumor

Role

alias

Name

PARAGANGLIOMA, CAROTID BODY

Role

alias

Name

PARAGANGLIOMA, FAMILIAL MALIGNANT

Role

alias

Name

PARAGANGLIOMAS, FAMILIAL NONCHROMAFFIN, 1

Role

alias

Name

PARAGANGLIOMAS, FAMILIAL, 1

Role

alias

Name

PARAGANGLIOMAS, HEREDITARY EXTRAADRENAL

Role

alias

Name

PARAGANGLIOMATA

Role

alias

Name

PGL

Role

alias

Name

PGL1

Role

alias

Name

PGL3

Role

alias

Name

PGL4

Role

alias

Name

PGL5

Role

alias

Name

PHEOCHROMOCYTOMA, EXTRAADRENAL, AND CERVICAL PARAGANGLIOMA

Role

alias

Name

PHEOCHROMOCYTOMA, FAMILIAL EXTRAADRENAL

Role

alias

Name

Paraganglioma, Extra-Adrenal

Role

alias

Name

Paragangliomas

Role

alias

Name

Paragangliomas 2

Role

alias

Name

Pgl2

Role

alias

Cross References

Trusted external identifiers retained for this final record.

Hpo

HP:0002668HP:0003001HP:0030074

Herb

HBDIS000474HBDIS001182HBDIS002290HBDIS002291HBDIS017026HBDIS017904HBDIS018318HBDIS018464HBDIS021107HBDIS021250

Me Sh

D002345D005925D010235D010236

Omim

115310168000601650605373614165

Umls

C0007279C0017671C0030421C0030422C1854336C1861848C1868633C3279992C3494181

Sym Map

SMDE00854SMDE02073SMDE03171SMDE04065SMDE06797SMDE08564SMDE09064SMDE11904SMDE11905

Do Class

DOID:14566DOID:630DOID:7

Dis Ge Net

C0007279C0017671C0030421C0030422C1854336C1861848C1866552C1868633C3276074C3279992

Umls Sty

T033T047T191

Hpo Class

HP:0000707HP:0000818HP:0002664

Me Sh Class

C04C09C10C16C23

Tcmbank Disease

11118148121617219166198522227823336258827403282919542

Itcmdb Generated

ITX-DISEASE-8711E5027100ITX-DISEASE-8ADD5140621A

Attributes

Merged source attributes and domain-specific metadata.

Version

v1v1,v2v2

Suppress

Do Class Name

genetic disease; disease of anatomical entity; disease of cellular proliferation

Disease Type

disease

Hpo Class Name

Abnormality of the endocrine system; Abnormality of the nervous system; Neoplasm

Do Disease Class

disease of anatomical entity; genetic disease; disease of cellular proliferation

Hpo Disease Class

Neoplasm; Abnormality of the nervous system; Abnormality of the endocrine system

Umls Disease Type

Disease or SyndromeFindingNeoplastic Process

Disease Definition

NCI2016_02D:A benign or malignant extra-adrenal parasympathetic paraganglioma arising from paraganglia in the base of the skull and middle ear.|MSH2017_2016_08_12:A paraganglioma involving the glomus jugulare, a microscopic collection of chemoreceptor tissue in the adventitia of the bulb of the jugular vein. It may cause paralysis of the vocal cords, attacks of dizziness, blackouts, and nystagmus. It is not resectable but radiation therapy is effective. It regresses slowly, but permanent control is regularly achieved. (From Dorland, 27th ed; Stedman, 25th ed; DeVita Jr et al., Cancer: Principles & Practice of Oncology, 3d ed, pp1603-4)NCI2016_02D:A benign or malignant paraganglioma arising from sympathetic or parasympathetic paraganglia outside the adrenal gland.|MSH2017_2016_08_12:A relatively rare, usually benign neoplasm originating in the chemoreceptor tissue of the CAROTID BODY; GLOMUS JUGULARE; GLOMUS TYMPANICUM; AORTIC BODIES; and the female genital tract. It consists histologically of rounded or ovoid hyperchromatic cells that tend to be grouped in an alveolus-like pattern within a scant to moderate amount of fibrous stroma and a few large thin-walled vascular channels. (From Stedman, 27th ed)NCI2016_CDISC_1602D:A neoplasm of the chemoreceptor system (e.g. carotid body, glomus jugulare, glomus vagale) for which the malignancy status has not be established.|NCI2016_02D:A benign or malignant extra-adrenal parasympathetic paraganglioma arising from paraganglia adjacent to or in the bifurcation of the common carotid artery. Most patients present with a slow growing, painless mass in the neck.|MSH2017_2016_08_12:Benign paraganglioma at the bifurcation of the COMMON CAROTID ARTERIES. It can encroach on the parapharyngeal space and produce dysphagia, pain, and cranial nerve palsies.|HPO2016_07_04:A usually benign neoplasm originating in the chemoreceptor tissue of the cartodi body, glomus jugulare, glomus tympanicum, aortic bodies, or the female genital tract. []NCI2016_NCI-GLOSS_1602D:A rare, usually benign tumor that develops from cells of the paraganglia. Paraganglia are a collection of cells that came from embryonic nervous tissue, and are found near the adrenal glands and some blood vessels and nerves. Paragangliomas that develop in the adrenal gland are called pheochromocytomas. Those that develop outside of the adrenal glands near blood vessels or nerves are called glomus tumors or chemodectomas.|NCI2016_CDISC_1602D:A neoplasm arising from paraganglia located along nerves composed of neoplastic neuroectodermal chromaffin cells, for which the malignancy status has not been established.|NCI2016_02D:A benign or malignant neoplasm arising from paraganglia located along the sympathetic or parasympathetic nerves. Infrequently, it may arise outside the usual distribution of the sympathetic and parasympathetic paraganglia. Tumors arising from the adrenal gland medulla are called pheochromocytomas. Morphologically, paragangliomas usually display a nesting (Zellballen) growth pattern. There are no reliable morphologic criteria to distinguish between benign and malignant paragangliomas. The only definitive indicator of malignancy is the presence of regional or distant metastases.|MSH2017_2016_08_12:A neural crest tumor usually derived from the chromoreceptor tissue of a paraganglion, such as the carotid body, or medulla of the adrenal gland (usually called a chromaffinoma or pheochromocytoma). It is more common in women than in men. (Stedman, 25th ed; from Segen, Dictionary of Modern Medicine, 1992)|HPO2016_07_04:A carotid body tumor (also called paraganglionoma or chemodectoma) is a tumor found in the upper neck at the branching of the carotid artery. They arise from the chemoreceptor organ (paraganglion) located in the adventitia of the carotid artery bifurcation. [HPO:probinson]

Me Sh Disease Class

Congenital, Hereditary, and Neonatal Diseases and Abnormalities; NeoplasmsNeoplasmsNervous System Diseases; Otorhinolaryngologic Diseases; Neoplasms; Pathological Conditions, Signs and Symptoms

Dis Ge Net Disease Type

disease

Disease Class Name Me Sh

Congenital, Hereditary, and Neonatal Diseases and Abnormalities; NeoplasmsNeoplasmsPathological Conditions, Signs and Symptoms; Neoplasms; Nervous System Diseases; Otorhinolaryngologic Diseases

Umls Semantic Type Name

Disease or SyndromeFindingNeoplastic Process