Overview
Ring chromosome Y 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.
Azoospermia
Very frequent (80-99%)HP:0000027
Cryptorchidism
Very frequent (80-99%)HP:0000028
Decreased function of male gonad
Very frequent (80-99%)HP:0000026
Female infertility
Very frequent (80-99%)HP:0008222
Impaired spermatogenesis
Very frequent (80-99%)HP:0008669
Male infertility
Very frequent (80-99%)HP:0003251
Abnormality of the female genitalia
Frequent (30-79%)HP:0010460
Abnormality of the male genitalia
Frequent (30-79%)HP:0010461
Ambiguous external genitalia
Frequent (30-79%)HP:0000062
Ambiguous genitalia due to virilization
Frequent (30-79%)HP:0000061
Ambiguous genitalia in males
Frequent (30-79%)HP:0000033
Decreased body height
Frequent (30-79%)HP:0004322
Hypospadias
Frequent (30-79%)HP:0000047
Pure gonadal dysgenesis
Frequent (30-79%)HP:0000133
Unilateral cryptorchidism
Frequent (30-79%)HP:0012741
Urogenital sinus anomaly
Frequent (30-79%)HP:0100779
Gonadoblastoma
Occasional (5-29%)HP:0000150
Gynaecomastia
Occasional (5-29%)HP:0000771
Obesity
Occasional (5-29%)HP:0001513
Perineal hypospadias
Occasional (5-29%)HP:0000051
Scrotal cleft
Occasional (5-29%)HP:0000048
Streak ovary
Occasional (5-29%)HP:0010464
Quick Facts
- SNOMED CT
- 763407008
- UMLS CUI
- C4706450
- Fully Specified Name
- Ring chromosome Y syndrome (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 22
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.