Sensorineural deafness and male infertility

disorder

SNOMED 700489002CUI C1970187

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.

Abnormal sperm development

Always present (100%)HP:0008669

Abnormal sperm tail morphology

Always present (100%)HP:0012868

Bilateral nerve deafness

Always present (100%)HP:0008619

Reduced sperm motility

Always present (100%)HP:0012207

Sperm head anomaly

Always present (100%)HP:0012865

Azoospermia

Very frequent (80-99%)HP:0000027

Male infertility

Very frequent (80-99%)HP:0003251

Sensorineural deafness

Very frequent (80-99%)HP:0000407

Interictal vestibular dysfunction

Excluded (<1%)HP:0001751

Related Conditions

Male infertility of chromosomal origin(parent)

Recessive sensorineural hearing loss(parent)

Recessive hereditary disorder (autosomal)(parent)

Reproductive system hereditary disorder(parent)

Hereditary hearing loss(parent)

Quick Facts

SNOMED CT: 700489002
UMLS CUI: C1970187
Fully Specified Name: Sensorineural deafness and male infertility (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 9

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.