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.
Melnick-Fraser syndrome
Very frequent (80-99%)
Morquio syndrome
Very frequent (80-99%)
Bart-Pumphrey syndrome
Always present (100%)
Gorham's disease
Occasional (5-29%)
Dubowitz's syndrome
Occasional (5-29%)
Listeriosis
Very rare (1-4%)
Klippel-Feil sequence
Frequent (30-79%)
Bardet-Biedl syndrome
Occasional (5-29%)
Mucopolysaccharidosis, MPS-IV-A
Autosomal dominant hypohidrotic ectodermal dysplasia syndrome
Arachnoiditis
Very frequent (80-99%)
Biotinidase deficiency
Occasional (5-29%)
Crigler-Najjar syndrome, type I
Occasional (5-29%)
Killian-Teschler-Nicola syndrome
Frequent (30-79%)
Hyperphosphatasemia with bone disease
Frequent (30-79%)
Coffin-Siris syndrome
Frequent (30-79%)
Friedreich's ataxia
Occasional (5-29%)
Fibrous dysplasia of bone
Very rare (1-4%)
Ménière's disease
Melnick-Needles syndrome
Frequent (30-79%)
Familial amyloid nephropathy with urticaria AND deafness
Always present (100%)
Coffin-Lowry syndrome
Always present (100%)
Mucopolysaccharidosis, MPS-III-D
Frequent (30-79%)
Fabry's disease
Very frequent (80-99%)
4p partial monosomy syndrome
Frequent (30-79%)
Related Symptoms
Quick Facts
- SNOMED CT
- 103276001
- UMLS CUI
- C1384666
- Fully Specified Name
- Decreased hearing (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.