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.
Rubinstein-Taybi syndrome
Always present (100%)
Leucocyte adhesion deficiency - type 2
Occasional (5-29%)
Neonatal pseudo-hydrocephalic progeroid syndrome
Very rare (1-4%)
Multiple symmetrical lipomatosis
Very rare (1-4%)
15q24 microdeletion
Frequent (30-79%)
Mowat-Wilson syndrome
Frequent (30-79%)
Trisomy 17p
Occasional (5-29%)
X-linked reticulate pigmentary disorder with systemic manifestation syndrome
Always present (100%)
Ramos Arroyo syndrome
Hirschsprung disease and intellectual disability due to del(2)(q22)
Frequent (30-79%)
Brain malformations, musculoskeletal abnormalities, facial dysmorphism, intellectual disability syndrome
Occasional (5-29%)
Congenital labioscrotal agenesis, cerebellar malformation, corneal dystrophy, facial dysmorphism syndrome
Very frequent (80-99%)
Arginine-glutamic acid dipeptide repeats-related neurodevelopmental syndrome
Occasional (5-29%)
Pilarowski Bjornsson syndrome
Frequent (30-79%)
Pyrroline-5-carboxylate reductase 2 related microcephaly, progressive leucoencephalopathy
Occasional (5-29%)
Microcephaly, intellectual disability, sensorineural deafness, epilepsy, abnormal muscle tone syndrome
Occasional (5-29%)
Megalencephaly, severe kyphoscoliosis, overgrowth syndrome
Very frequent (80-99%)
Quick Facts
- SNOMED CT
- 1142294009
- UMLS CUI
- C1856121
- Fully Specified Name
- Broad eyebrow (finding)
- Associated Conditions
- 17
- 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.