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.
Holoprosencephaly sequence
Frequent (30-79%)
Hypogonadotropic hypogonadism
Very frequent (80-99%)
Wilson's disease
Always present (100%)
Hypogonadism with anosmia
Very frequent (80-99%)
Multiple lentigines syndrome
Westphal-Strumpell syndrome
Always present (100%)
Free-living amoeba infection
Very rare (1-4%)
Young onset Parkinson disease
Occasional (5-29%)
Autosomal dominant late onset Parkinson disease
Frequent (30-79%)
Kufor Rakeb syndrome
Hyposmia, nasal and ocular hypoplasia, hypogonadotropic hypogonadism syndrome
Very frequent (80-99%)
HSAN8 - hereditary sensory and autonomic neuropathy type 8
Excluded (<1%)
Hyperostosis cranialis interna
SCPX (sterol carrier protein X) deficiency
Always present (100%)
Quick Facts
- SNOMED CT
- 83156004
- UMLS CUI
- C2364082
- Fully Specified Name
- Sense of smell impaired (finding)
- Associated Conditions
- 14
- 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.