Splenogonadal fusion

disorder

SNOMED 62042001CUI C0266636

Overview

Splenogonadal fusion 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 scrotum morphology

Very frequent (80-99%)HP:0000045

Testicular mass

Frequent (30-79%)HP:0032404

Unilateral cryptorchidism

Frequent (30-79%)HP:0012741

Abnormal epididymis morphology

Occasional (5-29%)HP:0009714

Cryptorchidism, bilateral

Occasional (5-29%)HP:0008689

Ectopia of the spleen

Occasional (5-29%)HP:0010452

Hydrocele testis

Occasional (5-29%)HP:0000034

Inguinal hernia

Occasional (5-29%)HP:0000023

Multiple accessory spleens

Occasional (5-29%)HP:0001748

Abnormality of the penis

Very rare (1-4%)HP:0000036

Related Conditions

Splenogonadal fusion, limb defect, micrognathia syndrome(child)

Congenital anomaly of spleen(parent)

Splenic lesion(parent)

Lesion of genitalia(parent)

Gonadal dysgenesis(parent)

Quick Facts

SNOMED CT: 62042001
UMLS CUI: C0266636
Fully Specified Name: Splenogonadal fusion (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 10

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.