Nonmosaic schwannomatosis

disorder

SNOMED 1332358007CUI C5779880

Overview

Nonmosaic schwannomatosis is a disorder.

Auto-generated from clinical reference data. Not a substitute for medical advice.

Signs & Symptoms

Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.

Schwannoma

Always present (100%)HP:0100008

Pain

Frequent (30-79%)HP:0012531

Peripheral schwannoma

Frequent (30-79%)HP:0009593

Spinal tumours

Frequent (30-79%)HP:0010302

Cataract

Occasional (5-29%)HP:0000518

Cobb angle greater than ten degrees

Occasional (5-29%)HP:0002650

Fatty lump

Occasional (5-29%)HP:0012032

Hypoacusis

Occasional (5-29%)HP:0000365

Lumbar/sacral hemangioma

Occasional (5-29%)HP:0410275

Muscle weakness

Occasional (5-29%)HP:0001324

Oncology

Occasional (5-29%)HP:0002664

Paresthesia

Occasional (5-29%)HP:0003401

Ringing in ears

Occasional (5-29%)HP:0000360

Uterine fibroid

Occasional (5-29%)HP:0000131

Hypoaesthesia

Very rare (1-4%)HP:0033748

Hypophonia

Very rare (1-4%)HP:0001621

Meningioma

Very rare (1-4%)HP:0002858

Muscle fasciculation

Very rare (1-4%)HP:0002380

Neoplasm of the pars anterior

Very rare (1-4%)HP:0011750

Seizures

Very rare (1-4%)HP:0001250

Related Conditions

Autosomal dominant hereditary disorder(parent)

Schwannoma(parent)

Neurofibromatosis syndrome(parent)

Hereditary disorder of the integument(parent)

Hereditary disorder of nervous system(parent)

Benign neoplasm of nervous system(parent)

Quick Facts

SNOMED CT: 1332358007
UMLS CUI: C5779880
Fully Specified Name: Full schwannomatosis (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 20

Medical Disclaimer

This information is for educational purposes only and does not constitute medical advice, diagnosis, or treatment. Always consult with a qualified healthcare provider regarding any medical condition or treatment plan.

Clinical content is derived from the SNOMED CT clinical ontology and curated medical knowledge graphs.