Overview
Bifid nasal tip is a finding that may indicate an underlying health condition requiring clinical evaluation.
Associated Conditions
Conditions associated with this symptom based on HPO disease-phenotype annotations.
Mohr syndrome
Frequent (30-79%)
Complete trisomy 18 syndrome
Microphthalmia, cataract, radiculomegaly and septal heart defect
Very frequent (80-99%)
Manitoba oculotrichoanal syndrome
Occasional (5-29%)
Craniofrontonasal dysplasia
Occasional (5-29%)
Acromelic frontonasal dysplasia
Very frequent (80-99%)
Frontofacionasal dysplasia syndrome
Frequent (30-79%)
Oro-facial digital syndrome type 9
BSG syndrome
Frequent (30-79%)
17q11.2 microduplication syndrome
Always present (100%)
Hypertelorism with microtia and facial clefting syndrome
Occasional (5-29%)
Intellectual disability, balding, patella luxation, acromicria syndrome
Oro-facial digital syndrome type 8
Autosomal dominant omodysplasia
Premature ageing appearance, developmental delay, cardiac arrhythmia syndrome
Occasional (5-29%)
Oculoauriculofrontonasal syndrome
Very frequent (80-99%)
Frontonasal dysplasia, bifid nose, upper limb anomalies syndrome
Frequent (30-79%)
Neurodevelopmental disorder, craniofacial dysmorphism, cardiac defect, skeletal anomalies syndrome
Frequent (30-79%)
ALX3-related frontonasal dysplasia
Autosomal dominant intellectual disability, craniofacial anomalies, cardiac defects syndrome
Occasional (5-29%)
EVEN-plus syndrome
Always present (100%)
Quick Facts
- SNOMED CT
- 249326006
- UMLS CUI
- C0426428
- Fully Specified Name
- Bifid nasal tip (finding)
- Associated Conditions
- 21
- 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.