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Frontonasal dysplasia, bifid nose, upper limb anomalies syndrome
disorderSNOMED 1177166006CUI C5567892
Overview
Frontonasal dysplasia, bifid nose, upper limb anomalies 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.
Abnormal hands
Frequent (30-79%)HP:0001155
Abnormality of the arm
Frequent (30-79%)HP:0002817
Almond shaped eyes
Frequent (30-79%)HP:0007874
Anomaly of the nasal bones
Frequent (30-79%)HP:0010939
Broad flat nasal bridge
Frequent (30-79%)HP:0000431
Decreased volume of upper lip
Frequent (30-79%)HP:0000219
Downturned corners of mouth
Frequent (30-79%)HP:0002714
Increased distance between eyes
Frequent (30-79%)HP:0000316
Increased nasal width
Frequent (30-79%)HP:0000445
Notched tip of nose
Frequent (30-79%)HP:0000456
Permanent curving of the pinkie finger
Frequent (30-79%)HP:0004209
Small for gestational age infant
Frequent (30-79%)HP:0001511
Small nasal alae
Frequent (30-79%)HP:0000430
Unbalanced face
Frequent (30-79%)HP:0000324
Absence of corpus callosum
Occasional (5-29%)HP:0001274
Atria septal defect
Occasional (5-29%)HP:0001631
Choanal atresia
Occasional (5-29%)HP:0000453
Clinodactyly of the 3rd toe
Occasional (5-29%)HP:0008115
Dropped arches
Occasional (5-29%)HP:0001763
Frontoethmoidal encephalocele
Occasional (5-29%)HP:0007330
Oligodactyly
Occasional (5-29%)HP:0012165
Related Conditions
Quick Facts
- SNOMED CT
- 1177166006
- UMLS CUI
- C5567892
- Fully Specified Name
- Frontonasal dysplasia, bifid nose, upper limb anomalies syndrome (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 21
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.