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Osteosclerosis, ichthyosis, premature ovarian failure syndrome
disorderSNOMED 722114007CUI C4302815
Overview
Osteosclerosis, ichthyosis, premature ovarian failure 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.
Dependant oedema
Very frequent (80-99%)HP:0010741
Ichthyosiform abnormality of the skin
Very frequent (80-99%)HP:0008064
Increased bone mineral density
Very frequent (80-99%)HP:0011001
Premature menopause
Very frequent (80-99%)HP:0008209
Related Conditions
Congenital ichthyosis of skin(parent)
Multiple system malformation syndrome(parent)
Premature ovarian failure(parent)
Dysplasia with increased bone density(parent)
Hereditary disorder of endocrine system(parent)
Hereditary disorder of musculoskeletal system(parent)
Reproductive system hereditary disorder(parent)
Congenital anomaly of skeletal bone(parent)
Quick Facts
- SNOMED CT
- 722114007
- UMLS CUI
- C4302815
- Fully Specified Name
- Sclerosing dysplasia of bone, ichthyosis, premature ovarian failure syndrome (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 4
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.