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.
Mohr syndrome
Frequent (30-79%)
Dubowitz's syndrome
Metaphyseal chondrodysplasia, McKusick type
Occasional (5-29%)
Killian-Teschler-Nicola syndrome
Very frequent (80-99%)
Macroencephaly
Very frequent (80-99%)
Aarskog syndrome
Frequent (30-79%)
Coffin-Lowry syndrome
Frequent (30-79%)
Hereditary orotic aciduria
Frequent (30-79%)
4p partial monosomy syndrome
Frequent (30-79%)
Leri-Weill dyschondrosteosis
Very frequent (80-99%)
Metaphyseal chondrodysplasia, Jansen type
Very frequent (80-99%)
Ascher's syndrome
Occasional (5-29%)
Greig cephalopolysyndactyly syndrome
Frequent (30-79%)
Marshall syndrome
Very frequent (80-99%)
Pineal hyperplasia AND diabetes mellitus syndrome
Occasional (5-29%)
Hyperphosphatasemia with mental retardation
Frequent (30-79%)
Sialic acid storage disease, severe infantile type
Hanhart's syndrome
Frequent (30-79%)
Craniometaphyseal dysplasia
Very frequent (80-99%)
XXXXY syndrome
Occasional (5-29%)
Mietens syndrome
Frequent (30-79%)
Langer-Giedion syndrome
Occasional (5-29%)
Cerebro-oculo-facio-skeletal syndrome
Very frequent (80-99%)
Penta X syndrome
Frequent (30-79%)
Smith-Lemli-Opitz syndrome
Very frequent (80-99%)
Quick Facts
- SNOMED CT
- 249321001
- UMLS CUI
- C0426421
- Fully Specified Name
- Wide nose (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.