Overview
Schöpf-Schulz-Passarge 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.
Dry skin
Always present (100%)HP:0000958
Dystrophic nails
Always present (100%)HP:0008404
Epidermal hyperkeratosis
Always present (100%)HP:0000962
Multiple eyelid-margin apocrine hidrocystomas
Always present (100%)HP:0034946
Sparse body hair
Always present (100%)HP:0002231
Facial telangiectasia
Very frequent (80-99%)HP:0007380
Keratoderma
Very frequent (80-99%)HP:0000982
Thin, sparse hair
Very frequent (80-99%)HP:0008070
Hair loss
Frequent (30-79%)HP:0001596
Missing between one and six teeth
Frequent (30-79%)HP:0000668
Premature exfoliation of primary teeth
Frequent (30-79%)HP:0006323
Sparse or absent eyebrows
Frequent (30-79%)HP:0100840
Basal cell carcinoma
Occasional (5-29%)HP:0002671
Bird-like facial appearance
Occasional (5-29%)HP:0000320
Ovarian cancer
Occasional (5-29%)HP:0100615
Squamous cell carcinoma
Occasional (5-29%)HP:0002860
Abnormal eye
HP:0000478
Apocrine hidrocystoma
HP:0031454
Ectodermal dysplasia
HP:0000968
Longitudinal ridging
HP:0001807
Narrow nail
HP:0011313
Oncholysis
HP:0001806
Poroma
HP:0031405
Small nail
HP:0001792
Thin nails
HP:0001816
Related Conditions
Hereditary neoplastic syndrome(parent)
Autosomal hereditary disorder(parent)
Developmental hereditary disorder(parent)
Hereditary disorder of tooth(parent)
Ectodermal dysplasia with hair-tooth-nail defects(parent)
Hereditary diffuse palmoplantar keratoderma(parent)
Genetic disorder of nail(parent)
Hypotrichosis(parent)
Dystrophia unguium(parent)
Hereditary disorder of the visual system(parent)
Congenital anomaly in number of teeth(parent)
Cyst of eyelid(parent)
Quick Facts
- SNOMED CT
- 700062000
- UMLS CUI
- C1857069
- Fully Specified Name
- Schöpf-Schulz-Passarge syndrome (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 25
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.