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.
Distal monosomy 1p36
Very frequent (80-99%)
Mowat-Wilson syndrome
Frequent (30-79%)
Retinal detachment and occipital encephalocele
Always present (100%)
7q11.23 microduplication syndrome
Occasional (5-29%)
Intellectual disability, obesity, brain malformation, facial dysmorphism syndrome
Frequent (30-79%)
Monosomy 13q34
Occasional (5-29%)
Tatton Brown Rahman overgrowth syndrome
Always present (100%)
Neonatal inflammatory skin and bowel disease
Frequent (30-79%)
AT-hook DNA binding motif containing 1-related intellectual disability, obstructive sleep apnea, mild dysmorphism syndrome
Frequent (30-79%)
Developmental delay, facial dysmorphism syndrome due to mediator complex subunit 13 like deficiency
Occasional (5-29%)
Infantile hypotonia, oculomotor anomalies, hyperkinetic movements, developmental delay syndrome
Occasional (5-29%)
FHEIG (facial dysmorphism, hypertrichosis, epilepsy, intellectual disability/developmental delay, gingival overgrowth) syndrome
Always present (100%)
Speech-language disorder type 1
Very rare (1-4%)
Quick Facts
- SNOMED CT
- 1142298007
- UMLS CUI
- C3277019
- Fully Specified Name
- Horizontal eyebrow (finding)
- Associated Conditions
- 13
- 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.