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.
Ruvalcaba syndrome
Autosomal dominant hypohidrotic ectodermal dysplasia syndrome
Hallermann-Streiff syndrome
Ectodermal dysplasia-ocular malformation syndrome
Oculodentodigital syndrome
Mietens syndrome
Diastrophic dysplasia
Occasional (5-29%)
Saethre-Chotzen syndrome
Mandibuloacral dysostosis
Very frequent (80-99%)
Neonatal pseudo-hydrocephalic progeroid syndrome
Frequent (30-79%)
Multiple symmetrical lipomatosis
Frequent (30-79%)
X-linked mental retardation with marfanoid habitus syndrome
Frequent (30-79%)
Roifman-Melamed syndrome
Dilated cardiomyopathy with hypergonadotropic hypogonadism syndrome
Always present (100%)
Van den Ende-Gupta syndrome
Frequent (30-79%)
Catel Manzke syndrome
Occasional (5-29%)
Syndactyly, telecanthus, anogenital and renal malformation syndrome
Monosomy 20q13.33
Occasional (5-29%)
Spondyloepiphyseal dysplasia, retinal dystrophy, immunodeficiency syndrome
Always present (100%)
Acroosteolysis, keloid-like lesions, premature ageing syndrome
Autosomal recessive cutis laxa type 2B
Always present (100%)
Cockayne syndrome type 3
Occasional (5-29%)
Quick Facts
- SNOMED CT
- 249322008
- UMLS CUI
- C0426422
- Fully Specified Name
- Narrow nose (finding)
- Associated Conditions
- 22
- 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.