Male infertility with teratozoospermia due to single gene mutation

disorder

SNOMED 764096006CUI C4706677

Overview

Male infertility with teratozoospermia due to single gene mutation 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 sperm development

Very frequent (80-99%)HP:0008669

Abnormal sperm tail morphology

Very frequent (80-99%)HP:0012868

Decreased testicular size

Very frequent (80-99%)HP:0008734

Globozoospermia

Very frequent (80-99%)HP:0012205

Gonadotropin excess

Very frequent (80-99%)HP:0000837

Phenotypic abnormality

Very frequent (80-99%)HP:0000118

Teratozoospermia

Very frequent (80-99%)HP:0012864

Testicular azoospermia

Very frequent (80-99%)HP:0011961

Related Conditions

Teratozoospermia(parent)

Male infertility of genetic origin(parent)

Male genital organ disease(parent)

Quick Facts

SNOMED CT: 764096006
UMLS CUI: C4706677
Fully Specified Name: Male infertility with teratozoospermia due to single gene mutation (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 8

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.