Overview
Deafness and hypogonadism 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.
Abnormal sperm development
Very frequent (80-99%)HP:0008669
Abnormality of the internal auditory canal
Very frequent (80-99%)HP:0011384
Delayed puberty
Very frequent (80-99%)HP:0000823
Enlarged cochlear aqueduct
Very frequent (80-99%)HP:0011388
Hearing loss, conductive
Very frequent (80-99%)HP:0000405
Ossicular malformation
Very frequent (80-99%)HP:0004452
Primary hypogonadism
Very frequent (80-99%)HP:0000815
Progressive bilateral sensorineural hearing loss
Very frequent (80-99%)HP:0000408
Retarded ossification
Very frequent (80-99%)HP:0002750
Severe conductive hearing impairment
Very frequent (80-99%)HP:0012717
Stapes ankylosis
Very frequent (80-99%)HP:0000381
Behavioral changes
Frequent (30-79%)HP:0000708
Heterochromia iridis
Occasional (5-29%)HP:0001100
Increased distance between eyes
Occasional (5-29%)HP:0000316
Intellectual impairment
Occasional (5-29%)HP:0100543
Night blindness, congenital
Occasional (5-29%)HP:0007642
Palpebronasal fold
Occasional (5-29%)HP:0000286
Reduced blood thiamine level
Occasional (5-29%)HP:0100503
Related Conditions
Quick Facts
- SNOMED CT
- 718714006
- UMLS CUI
- C1844680
- Fully Specified Name
- Deafness and hypogonadism syndrome (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 18
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.