Overview
Caudal appendage deafness 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.
Abnormality of digit
Frequent (30-79%)HP:0011297
Coccygeal tail
Frequent (30-79%)HP:0002825
Cryptorchidism
Frequent (30-79%)HP:0000028
Decreased body height
Frequent (30-79%)HP:0004322
Distortion of face
Frequent (30-79%)HP:0001999
Dull intelligence
Frequent (30-79%)HP:0001249
Infantile sensorineural hearing impairment
Frequent (30-79%)HP:0008610
Related Conditions
Brachyphalangia(parent)
Multiple malformation syndrome with limb defect as major feature(parent)
Congenital anomaly of caudal vertebra(parent)
Undescended testicle(parent)
Hearing loss associated with syndrome(parent)
Small stature(parent)
Congenital hearing disorder(parent)
Genetic intellectual disability(parent)
Quick Facts
- SNOMED CT
- 726621009
- UMLS CUI
- C2931593
- Fully Specified Name
- Caudal appendage deafness syndrome (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 7
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.