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.
Septo-optic dysplasia sequence
Occasional (5-29%)
Levy-Hollister syndrome
Very rare (1-4%)
Phytanic acid storage disease
Very frequent (80-99%)
Holoprosencephaly sequence
Frequent (30-79%)
Hypogonadotropic hypogonadism
Very frequent (80-99%)
Kartagener syndrome
CHARGE association
Very frequent (80-99%)
Obstructive sleep apnea syndrome
Immotile cilia syndrome
Hypogonadism with anosmia
Very frequent (80-99%)
Hereditary sensory and motor neuropathy, type VI
Congenital anosmia
Solitary median maxillary central incisor syndrome
Occasional (5-29%)
Blepharophimosis, ptosis, esotropia, syndactyly, short stature syndrome
Occasional (5-29%)
8p11.2 deletion syndrome
Occasional (5-29%)
Brachytelephalangy, facial dysmorphism, Kallmann syndrome
Frequent (30-79%)
Johnson McMillin syndrome
Occasional (5-29%)
Kufor Rakeb syndrome
Hyposmia, nasal and ocular hypoplasia, hypogonadotropic hypogonadism syndrome
Very frequent (80-99%)
Superficial siderosis of central nervous system
Occasional (5-29%)
Peripheral demyelinating neuropathy, central dysmyelinating leukodystrophy, Waardenburg syndrome, Hirschsprung disease
Brachytelephalangic chondrodysplasia punctata
Hyperostosis cranialis interna
Frequent (30-79%)
Quick Facts
- SNOMED CT
- 44169009
- UMLS CUI
- C0003126
- Fully Specified Name
- Loss of sense of smell (finding)
- Associated Conditions
- 23
- 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.