Overview
Sengers Hamel Otten 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.
Decreased body height
Always present (100%)HP:0004322
Gynaecomastia
Always present (100%)HP:0000771
Hypoplastic fourth metacarpal
Always present (100%)HP:0010044
Low posterior hair line
Always present (100%)HP:0002162
Mental retardation, mild
Always present (100%)HP:0001256
Mitral valve prolapse
Always present (100%)HP:0001634
Narrow, high-arched roof of mouth
Always present (100%)HP:0002705
Nonsyndromal hydrocephalus
Always present (100%)HP:0000238
Obesity
Always present (100%)HP:0001513
Outward turned elbows
Always present (100%)HP:0002967
Primary hypogonadism
Always present (100%)HP:0000815
Short neck
Always present (100%)HP:0000470
Abnormality of the hypothalamus-pituitary axis
Frequent (30-79%)HP:0000864
Absent facial hair
Frequent (30-79%)HP:0002550
Azoospermia
Frequent (30-79%)HP:0000027
Sparse facial hair
Frequent (30-79%)HP:0007464
Related Conditions
Congenital hydrocephalus(parent)
Multiple system malformation syndrome(parent)
Centripetal obesity(parent)
Hereditary disorder of endocrine system(parent)
Hereditary disorder of nervous system(parent)
Reproductive system hereditary disorder(parent)
Primary hypogonadism(parent)
Developmental hereditary disorder(parent)
X-linked recessive hereditary disease(parent)
Genetic obesity disorder(parent)
Quick Facts
- SNOMED CT
- 721231007
- UMLS CUI
- C4303476
- Fully Specified Name
- Hydrocephalus with obesity and hypogonadism syndrome (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 16
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.