DiseaseID 4726

神经纤维瘤

disease

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Disease: 1Symptom: 5Target: 12Links: 17

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Record Fields

Scalar fields from the final disease record.

Disease Id: 4726
Core Entity Id: 61118
Source Entity Count: 1
Preferred Name: Neurofibroma
Name Cn: 神经纤维瘤
Name Pinyin: Shen Jing Xian Wei Liu
Name En: Neurofibroma
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
Mesh Class Name: Neoplasms; Nervous System Diseases
Hpo Class Name
Do Class Name: disease of anatomical entity; disease of cellular proliferation
Disease Definition: NCI2016_NCI-GLOSS_1602D:A benign tumor that develops from the cells and tissues that cover nerves.|NCI2016_CDISC_1602D:An intraneural or extraneural neoplasm arising from nerve tissues and neural sheaths, composed of perineurial-like fibroblasts and Schwann cells.|NCI2016_02D:An intraneural or extraneural neoplasm arising from nerve tissues and neural sheaths. It is composed of perineurial-like fibroblasts and Schwann cells. It usually presents as a localized cutaneous lesion and less often as a circumscribed peripheral nerve mass. Patients with neurofibromatosis type 1 present with multiple masses. Neurofibromas which arise from major nerves and plexiform neurofibromas are precursor lesions to malignant peripheral nerve sheath tumors.|MSH2017_2016_08_12:A moderately firm, benign, encapsulated tumor resulting from proliferation of SCHWANN CELLS and FIBROBLASTS that includes portions of nerve fibers. The tumors usually develop along peripheral or cranial nerves and are a central feature of NEUROFIBROMATOSIS 1, where they may occur intracranially or involve spinal roots. Pathologic features include fusiform enlargement of the involved nerve. Microscopic examination reveals a disorganized and loose cellular pattern with elongated nuclei intermixed with fibrous strands. (From Adams et al., Principles of Neurology, 6th ed, p1016)|CSP2006:moderately firm, benign, encapsulated tumor resulting from proliferation of Schwann cells and fibroblasts that includes portions of nerve fibers; tumors usually develop along peripheral or cranial nerves and are a central feature of neurofibromatosis 1, where they may occur intracranially or involve spinal roots. pathologic features include fusiform enlargement of the involved nerve.
Version: v2
Suppressed: No

Names

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

Name

Neurofibroma

Role

preferred

Cross References

Trusted external identifiers retained for this final record.

Herb

HBDIS002112

Me Sh

D009455

Umls

C0027830

Sym Map

SMDE11438

Do Class

DOID:14566DOID:7

Dis Ge Net

C0027830

Umls Sty

T191

Me Sh Class

C04C10

Tcmbank Disease

30697

Attributes

Merged source attributes and domain-specific metadata.

Version

Suppress

Do Class Name

disease of anatomical entity; disease of cellular proliferation

Disease Type

disease

Do Disease Class

disease of anatomical entity; disease of cellular proliferation

Umls Disease Type

Neoplastic Process

Disease Definition

NCI2016_NCI-GLOSS_1602D:A benign tumor that develops from the cells and tissues that cover nerves.|NCI2016_CDISC_1602D:An intraneural or extraneural neoplasm arising from nerve tissues and neural sheaths, composed of perineurial-like fibroblasts and Schwann cells.|NCI2016_02D:An intraneural or extraneural neoplasm arising from nerve tissues and neural sheaths. It is composed of perineurial-like fibroblasts and Schwann cells. It usually presents as a localized cutaneous lesion and less often as a circumscribed peripheral nerve mass. Patients with neurofibromatosis type 1 present with multiple masses. Neurofibromas which arise from major nerves and plexiform neurofibromas are precursor lesions to malignant peripheral nerve sheath tumors.|MSH2017_2016_08_12:A moderately firm, benign, encapsulated tumor resulting from proliferation of SCHWANN CELLS and FIBROBLASTS that includes portions of nerve fibers. The tumors usually develop along peripheral or cranial nerves and are a central feature of NEUROFIBROMATOSIS 1, where they may occur intracranially or involve spinal roots. Pathologic features include fusiform enlargement of the involved nerve. Microscopic examination reveals a disorganized and loose cellular pattern with elongated nuclei intermixed with fibrous strands. (From Adams et al., Principles of Neurology, 6th ed, p1016)|CSP2006:moderately firm, benign, encapsulated tumor resulting from proliferation of Schwann cells and fibroblasts that includes portions of nerve fibers; tumors usually develop along peripheral or cranial nerves and are a central feature of neurofibromatosis 1, where they may occur intracranially or involve spinal roots. pathologic features include fusiform enlargement of the involved nerve.

Me Sh Disease Class

Nervous System Diseases; Neoplasms

Dis Ge Net Disease Type

disease

Disease Class Name Me Sh

Neoplasms; Nervous System Diseases

Umls Semantic Type Name

Neoplastic Process