Overview
Difficulty chewing is a finding that may indicate an underlying health condition requiring clinical evaluation.
Associated Conditions
Conditions associated with this symptom based on HPO disease-phenotype annotations.
Gorham's disease
Frequent (30-79%)
Glycogen storage disease, type V
Very rare (1-4%)
Amelogenesis imperfecta
Frequent (30-79%)
Myasthenia gravis
Merosin deficient congenital muscular dystrophy
Frequent (30-79%)
Congenital myopathy with fibre type disproportion
Occasional (5-29%)
Glycogen heart disease
Occasional (5-29%)
Cleft lip and cleft of alveolar process of maxilla
Frequent (30-79%)
Temporal arteritis
Very frequent (80-99%)
Giant cell arteritis
Very frequent (80-99%)
Hemifacial hyperplasia
Occasional (5-29%)
Rutherfurd syndrome
Frequent (30-79%)
Auriculo-condylar syndrome
Infantile-onset ascending hereditary spastic paralysis
Very frequent (80-99%)
Genetic recurrent myoglobinuria
Occasional (5-29%)
Combined oxidative phosphorylation defect type 7
Occasional (5-29%)
Helsmoortel-van der Aa syndrome
Occasional (5-29%)
HMNDYT2 - hypermanganesemia with dystonia 2
Always present (100%)
AT-hook DNA binding motif containing 1-related intellectual disability, obstructive sleep apnea, mild dysmorphism syndrome
Always present (100%)
Dystonia aphonia syndrome
Very frequent (80-99%)
Pontine tegmental cap dysplasia
Cortical dysgenesis with pontocerebellar hypoplasia due to TUBB3 mutation
Occasional (5-29%)
Merosin-negative congenital muscular dystrophy
Frequent (30-79%)
Oligodontia
Very frequent (80-99%)
Bilateral generalized polymicrogyria
Occasional (5-29%)
Related Symptoms
Quick Facts
- SNOMED CT
- 162020001
- UMLS CUI
- C0239043
- Fully Specified Name
- Difficulty chewing (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.