Pineoblastoma

disorder

SNOMED 767448007CUI C0205898

Overview

Source: MedlinePlus.gov, National Library of Medicine. Not a substitute for medical advice.

Signs & Symptoms

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

Pinealoma

Always present (100%)HP:0010799

Headache

Very frequent (80-99%)HP:0002315

Behavioral changes

Frequent (30-79%)HP:0000708

Cognitive deficits

Frequent (30-79%)HP:0100543

Intracranial hypertension

Frequent (30-79%)HP:0002516

Memory loss

Frequent (30-79%)HP:0002354

Worsening neurological symptoms

Frequent (30-79%)HP:0002344

Amaurosis fugax

Occasional (5-29%)HP:0100576

Convergence insufficiency

Occasional (5-29%)HP:0000619

Decreased visual acuity

Occasional (5-29%)HP:0007663

Epilepsy

Occasional (5-29%)HP:0001250

Midline brain calcifications

Occasional (5-29%)HP:0007045

Papillitis

Occasional (5-29%)HP:0001085

Paralysis

Occasional (5-29%)HP:0003470

Progressive visual field defects

Occasional (5-29%)HP:0007987

Retinoblastoma

Occasional (5-29%)HP:0009919

Sensory neuropathy

Occasional (5-29%)HP:0000763

Disturbances of consciousness

Very rare (1-4%)HP:0004372

Dullness

Very rare (1-4%)HP:0001254

Related Conditions

Pineal parenchymal tumor of intermediate differentiation(child)

Primary pineoblastoma(child)

Malignant tumour of pineal gland(parent)

NEN - neuroendocrine neoplasm(parent)

Quick Facts

SNOMED CT: 767448007
UMLS CUI: C0205898
Fully Specified Name: Pineoblastoma (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 19

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.