Overview
Eiken 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.
Acetabular angle flat
Always present (100%)HP:0003180
Broad femoral neck
Always present (100%)HP:0006429
Broad ribs
Always present (100%)HP:0000885
Bulging forehead
Always present (100%)HP:0011220
Chiari malformation
Always present (100%)HP:0002308
Clinodactyly
Always present (100%)HP:0030084
Decreased height of philtrum
Always present (100%)HP:0000322
Decreased projection of midface
Always present (100%)HP:0011800
Deficient in vitamin D
Always present (100%)HP:0100512
Delayed ankle bone maturation
Always present (100%)HP:0008103
Delayed loss of deciduous teeth
Always present (100%)HP:0006335
Delayed ossification of carpal bones
Always present (100%)HP:0001216
Dolichocephaly
Always present (100%)HP:0000268
Elevated alkaline phosphatase
Always present (100%)HP:0003155
Eruption failure
Always present (100%)HP:0000706
Failure of eruption of multiple teeth
Always present (100%)HP:0006283
Febrile seizure (within the age range of 3 months to 6 years)
Always present (100%)HP:0002373
Flat end part of bone
Always present (100%)HP:0003071
Increased distance between eyes
Always present (100%)HP:0000316
Increased height of lower lip vermilion
Always present (100%)HP:0000179
Increased thickness of cranium
Always present (100%)HP:0002684
Large halluces
Always present (100%)HP:0001847
Long thumb
Always present (100%)HP:0032524
Low body weight
Always present (100%)HP:0004325
Multiple buried teeth
Always present (100%)HP:0001571
No development of motor milestones
Always present (100%)HP:0001270
Partial anodontia
Always present (100%)HP:0000677
Pseudoepiphyses
Always present (100%)HP:0010584
Short middle phalanx of finger
Always present (100%)HP:0005819
Type A1 brachydactyly
Always present (100%)HP:0009371
Quick Facts
- SNOMED CT
- 720863002
- UMLS CUI
- C1838779
- Fully Specified Name
- Eiken syndrome (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 30
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.