Experimental Factor Ontology

Last uploaded: April 15, 2024
Preferred Name

schwannoma

Synonyms

neurolemmoma

SCHW

Neurilemmoma, NOS

Benign Schwannoma

Neurilemoma (morphologic abnormality)

Ancient neurilemoma

Psammomatous schwannoma

Degenerated Neurilemmoma

Ancient schwannoma

Pigmented Schawnnoma

Ancient neurilemmoma

Acoustic neuroma

Benign Neurilemmoma

Schwannomas

Melanotic schwannoma

Neurilemoma, Malignant

Cellular schwannoma

Schwannomatosis, Plexiform

Neurilemmomas

Neurilemmoma

Malignant Neurilemoma

Neurilemmosarcoma

Pigmented schwannoma

Degenerated Schwannoma

Plexiform schwannoma

Schwannoma (WHO Grade I)

Plexiform Schwannomatoses

Neurilemmoma (disorder)

Malignant Neurilemomas

Neurilemomas, Malignant

Neurilemmosarcomas

Ancient neurilemmoma (disorder)

Schwannoma, NOS

Neurilemomas

Neurilemoma

Ancient schwannoma (morphologic abnormality)

Melanocytic Schwannoma

Plexiform Schwannomatosis

Schwannomatoses, Plexiform

Neurinoma

Neurinomas

peripheral fibroblastoma

benign schwannoma

neurilemmoma

schwannoma, benign

schwannoma (WHO grade I)

benign neurilemmoma

psammomatous schwannoma

neurinoma

schwannoma

Definitions

A neoplasm that arises from SCHWANN CELLS of the cranial, peripheral, and autonomic nerves. Clinically, these tumors may present as a cranial neuropathy, abdominal or soft tissue mass, intracranial lesion, or with spinal cord compression. Histologically, these tumors are encapsulated, highly vascular, and composed of a homogenous pattern of biphasic fusiform-shaped cells that may have a palisaded appearance. (From DeVita Jr et al., Cancer: Principles and Practice of Oncology, 5th ed, pp964-5) A benign, usually encapsulated slow growing tumor of the peripheral nervous system composed of well differentiated Schwann cells. It recurs infrequently and only rare cases associated with malignant transformation have been reported. A neoplasm that arises from SCHWANN CELLS of the cranial, peripheral, and autonomic nerves. Clinically, these tumors may present as a cranial neuropathy, abdominal or soft tissue mass, intracranial lesion, or with spinal cord compression. Histologically, these tumors are encapsulated, highly vascular, and composed of a homogenous pattern of biphasic fusiform-shaped cells that may have a palisaded appearance (MeSH). A tumor of the peripheral nervous system composed of neoplastic Schwann cells. The vast majority of schwannomas follow a benign clinical course. Only rare cases associated with a malignant clinical course have been reported. A benign, usually encapsulated slow growing tumor composed of Schwann cells. It affects peripheral and cranial nerves. It recurs infrequently and only rare cases associated with malignant transformation have been reported.

ID

http://www.ebi.ac.uk/efo/EFO_0000693

closeMatch

http://identifiers.org/meddra/10029235

http://identifiers.org/meddra/10029234

database_cross_reference

SNOMEDCT:404022001

SNOMEDCT:985004

NIFSTD:birnlex_12603

SNOMEDCT:253086004

MedDRA:10039667

SNOMEDCT:404023006

SNOMEDCT:409704009

MeSH:D009442

OMIM:162091

SNOMEDCT:253087008

SNOMEDCT:253088003

SNOMEDCT:126949007

SNOMEDCT:77418004

DOID:12689

DOID:3192

DOID:3196

DOID:3206

DOID:955

NCIt:C3269

MedDRA:10029235

ICDO:9560/0

GARD:4767

UMLS:C0027809

NCIT:C3269

MedDRA:10029234

Orphanet:252164

MONDO:0002546

ONCOTREE:SCHW

SCTID:404022001

ICD9:215.9

definition

A neoplasm that arises from SCHWANN CELLS of the cranial, peripheral, and autonomic nerves. Clinically, these tumors may present as a cranial neuropathy, abdominal or soft tissue mass, intracranial lesion, or with spinal cord compression. Histologically, these tumors are encapsulated, highly vascular, and composed of a homogenous pattern of biphasic fusiform-shaped cells that may have a palisaded appearance. (From DeVita Jr et al., Cancer: Principles and Practice of Oncology, 5th ed, pp964-5)

A benign, usually encapsulated slow growing tumor of the peripheral nervous system composed of well differentiated Schwann cells. It recurs infrequently and only rare cases associated with malignant transformation have been reported.

A neoplasm that arises from SCHWANN CELLS of the cranial, peripheral, and autonomic nerves. Clinically, these tumors may present as a cranial neuropathy, abdominal or soft tissue mass, intracranial lesion, or with spinal cord compression. Histologically, these tumors are encapsulated, highly vascular, and composed of a homogenous pattern of biphasic fusiform-shaped cells that may have a palisaded appearance (MeSH).

A tumor of the peripheral nervous system composed of neoplastic Schwann cells. The vast majority of schwannomas follow a benign clinical course. Only rare cases associated with a malignant clinical course have been reported.

A benign, usually encapsulated slow growing tumor composed of Schwann cells. It affects peripheral and cranial nerves. It recurs infrequently and only rare cases associated with malignant transformation have been reported.

exactMatch

http://purl.obolibrary.org/obo/NCIT_C3269

http://purl.obolibrary.org/obo/DOID_3192

http://purl.obolibrary.org/obo/Orphanet_252164

http://purl.obolibrary.org/obo/DOID_955

http://linkedlifedata.com/resource/umls/id/C0027809

http://identifiers.org/snomedct/404022001

has_exact_synonym

Neurilemmoma, NOS

Benign Schwannoma

Neurilemoma (morphologic abnormality)

Ancient neurilemoma

Psammomatous schwannoma

Degenerated Neurilemmoma

Ancient schwannoma

Pigmented Schawnnoma

Ancient neurilemmoma

Acoustic neuroma

Benign Neurilemmoma

Schwannomas

Melanotic schwannoma

Neurilemoma, Malignant

Cellular schwannoma

Schwannomatosis, Plexiform

Neurilemmomas

Neurilemmoma

Malignant Neurilemoma

Neurilemmosarcoma

Pigmented schwannoma

Degenerated Schwannoma

Plexiform schwannoma

Schwannoma (WHO Grade I)

Plexiform Schwannomatoses

Neurilemmoma (disorder)

Malignant Neurilemomas

Neurilemomas, Malignant

Neurilemmosarcomas

Ancient neurilemmoma (disorder)

Schwannoma, NOS

Neurilemomas

Neurilemoma

Ancient schwannoma (morphologic abnormality)

Melanocytic Schwannoma

Plexiform Schwannomatosis

Schwannomatoses, Plexiform

Neurinoma

Neurinomas

peripheral fibroblastoma

benign schwannoma

neurilemmoma

schwannoma, benign

schwannoma (WHO grade I)

benign neurilemmoma

psammomatous schwannoma

neurinoma

schwannoma

has_related_synonym

neurolemmoma

SCHW

id

EFO:0000693

in_subset

http://purl.obolibrary.org/obo/mondo#ordo_disease

http://purl.obolibrary.org/obo/mondo#rare

http://purl.obolibrary.org/obo/mondo#nord_rare

http://purl.obolibrary.org/obo/mondo#orphanet_rare

http://purl.obolibrary.org/obo/mondo#gard_rare

label

schwannoma

notation

EFO:0000693

preferred label

schwannoma

prefLabel

schwannoma

see also

https://rarediseases.info.nih.gov/diseases/4767/schwannoma

term editor

Tomasz Adamusiak

James Malone

subClassOf

http://purl.obolibrary.org/obo/MONDO_0021637

http://purl.obolibrary.org/obo/MONDO_0002547

http://purl.obolibrary.org/obo/MONDO_0016752

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