Congenital absence of both testes

disorder

SNOMED 371015003CUI C1261504

Overview

Congenital absence of both testes 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 vas deferens morphology

Very frequent (80-99%)HP:0012872

Absent external genitalia

Very frequent (80-99%)HP:0000042

Absent testis

Very frequent (80-99%)HP:0010469

Decreased testosterone

Very frequent (80-99%)HP:0040171

Gonadotropin excess

Very frequent (80-99%)HP:0000837

Short penis

Very frequent (80-99%)HP:0000054

Vanishing testis

Very frequent (80-99%)HP:0012870

Ambiguous external genitalia

Frequent (30-79%)HP:0000062

Underdeveloped uterus

Frequent (30-79%)HP:0000013

Urethrovaginal fistulae

Frequent (30-79%)HP:0008716

Urogenital sinus anomaly

Frequent (30-79%)HP:0100779

Related Conditions

Bilateral testicular agenesis(child)

Left congenital monorchism(parent)

Congenital absence of right testis(parent)

Quick Facts

SNOMED CT: 371015003
UMLS CUI: C1261504
Fully Specified Name: Congenital absence of both testes (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 11

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.