OMOP Concept 1075851
Full schwannomatosis
StandardConditionSNOMED1332358007Disorder
Maps from
3
Descendants
0
Valid from
1 May 2024
Valid to
31 Dec 2099
OMOP concepts
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Source codes that map to this concept
3 source codes normalize to Full schwannomatosis via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| ICD10CM | Q85.03 | Schwannomatosis | Non-standard |
| ICD9CM | 237.73 | Schwannomatosis | Non-standard |
| MeSH | C536641 | Schwannomatosis | Non-standard |
Synonyms
Alternative names recorded for Full schwannomatosis across source vocabularies.
- Full neurofibromatosis type 3
- Full NF3 (neurofibromatosis type 3)
- Full schwannomatosis (disorder)
- Full SWN (schwannomatosis)
- Neurilemmomatosis
- neurilemomatosis
- neurofibromatosis tipo 3 completa
- NF3 (neurofibromatosis tipo 3) completa
- Nonmosaic schwannomatosis
- schwannomatosis completa
- schwannomatosis completa (trastorno)
- schwannomatosis sin mosaicismo
- SWN (schwannomatosis) completa
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(50)Roll up to these when you need a wider cohort.
- 1Autosomal dominant hereditary disorder
- 1Hereditary disorder of nervous system
- 1Hereditary disorder of the integument
- 1Neurofibromatosis syndrome
- 1Schwannoma
- 2Autosomal hereditary disorder
- 2Benign neoplasm of nerve sheath origin
- 2Benign neoplasm of nervous system
- 2Disorder of integument
- 2Disorder of nervous system
- 2Hereditary disorder by system
- 2Neoplasm of nerve sheath origin
- 2Neoplasm of uncertain behavior of nervous system
- 2Neoplasm of uncertain behavior of skin
- 2Neurocutaneous syndrome
- 2Skin tumor of neural origin
- 3Benign neoplastic disease
- 3Congenital disease
- 3Disorder of body system
- 3Fetal and/or neonatal disorder of integument
- 3Hereditary disease
- 3Integumentary system finding
- 3Neoplasm of nervous system
- 3Neoplasm of skin
- 3Neoplasm of uncertain behavior of soft tissues
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