Neutropenia, monocytopenia, deafness syndrome

disorder

SNOMED 725137007CUI C4518430

Overview

Neutropenia, monocytopenia, deafness syndrome 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.

Abnormal macrophage morphology

Very frequent (80-99%)HP:0004311

Abnormality of neutrophils

Very frequent (80-99%)HP:0001874

Sensorineural deafness

Very frequent (80-99%)HP:0000407

Abnormality of immune system physiology

Frequent (30-79%)HP:0010978

Related Conditions

Congenital deafness(parent)

Hearing loss associated with syndrome(parent)

Congenital neutropenia(parent)

Congenital anomaly of ear with impairment of hearing(parent)

Congenital anomaly of inner ear(parent)

Quick Facts

SNOMED CT: 725137007
UMLS CUI: C4518430
Fully Specified Name: Neutropenia, monocytopenia, deafness syndrome (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 4

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.