Overview
Clinical overview and emergency guidance are pending physician authorship. Graph-derived data (ontology codes, linked conditions, diagnostic biomarkers) is available below.
Associated Conditions
Conditions associated with this symptom based on HPO disease-phenotype annotations.
Coffin-Lowry syndrome
4p partial monosomy syndrome
Frequent (30-79%)
Holoprosencephaly sequence
Occasional (5-29%)
Hyperphosphatasemia with mental retardation
Occasional (5-29%)
De Lange syndrome
Very frequent (80-99%)
Rubinstein-Taybi syndrome
Frequent (30-79%)
CHARGE association
Occasional (5-29%)
Congenital muscular hypertrophy-cerebral syndrome
Mannosidosis, type I
Occasional (5-29%)
Marshall-Smith syndrome
Frequent (30-79%)
20p partial trisomy syndrome
Very frequent (80-99%)
Familial aplasia of the vermis
Occasional (5-29%)
Kabuki make-up syndrome
Very frequent (80-99%)
Raine dysplasia
Occasional (5-29%)
Nicolaides-Baraitser syndrome
Frequent (30-79%)
Microphthalmia, cataract, radiculomegaly and septal heart defect
Occasional (5-29%)
Chromosome 1q21.1 deletion syndrome
Very rare (1-4%)
Facial dysmorphism, intellectual deficit, short stature and hearing loss
Always present (100%)
Zimmermann-Laband syndrome
Frequent (30-79%)
Chromosome 2q37 deletion syndrome
Spondyloepiphyseal dysplasia, Omani type
Frequent (30-79%)
Char syndrome
Blepharophimosis epicanthus inversus ptosis syndrome
Growth delay due to insulin-like growth factor I resistance
Pseudoaminopterin syndrome
Quick Facts
- SNOMED CT
- 1142297002
- UMLS CUI
- C1868571
- Fully Specified Name
- High arched eyebrow (finding)
- Associated Conditions
- 25
- Diagnostic Tests
- 0
This information is for educational purposes only. If you are experiencing symptoms, please consult a healthcare provider for proper evaluation and diagnosis.