Overview
Shokeir 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 the eyelashes
Very frequent (80-99%)HP:0000499
Alopecia universalis
Very frequent (80-99%)HP:0002289
Dental problems
Very frequent (80-99%)HP:0000164
Electroencephalogram abnormal
Very frequent (80-99%)HP:0002353
Memory impairment
Very frequent (80-99%)HP:0002354
Mental retardation, mild
Very frequent (80-99%)HP:0001256
Periodontal disease
Very frequent (80-99%)HP:0000704
Red and swollen gums
Very frequent (80-99%)HP:0000230
Sparse body hair
Very frequent (80-99%)HP:0002231
Thinning scalp hair
Very frequent (80-99%)HP:0002209
Epilepsy
Frequent (30-79%)HP:0001250
Hypoacusis
Occasional (5-29%)HP:0000365
Nevocellular nevi
Occasional (5-29%)HP:0000995
Nonsyndromal hydrocephalus
Occasional (5-29%)HP:0000238
Related Conditions
Congenital alopecia(parent)
Autosomal dominant hereditary disorder(parent)
Alopecia universalis(parent)
Hereditary disorder of the integument(parent)
Periodontitis co-occurrent with genetic disorder(parent)
Congenital anomaly of digestive organ(parent)
Congenital anomaly of jaw(parent)
Congenital abnormality of oral cavity(parent)
Developmental hereditary disorder(parent)
Developmental anomaly of periodontal tissue(parent)
Hereditary disorder of immune system(parent)
Quick Facts
- SNOMED CT
- 720980004
- UMLS CUI
- C1863090
- Fully Specified Name
- Alopecia, psychomotor epilepsy, periodontal pyorrhea, intellectual disability syndrome (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 14
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.