Overview
Mutism 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.
Neuroleptic malignant syndrome
Very frequent (80-99%)
Progressive supranuclear ophthalmoplegia
Mietens syndrome
Very frequent (80-99%)
Arthrochalasis multiplex congenita
Very frequent (80-99%)
Huntington's chorea
Occasional (5-29%)
Farber's lipogranulomatosis
Occasional (5-29%)
Kleine-Levin syndrome
Occasional (5-29%)
Progressive supranuclear palsy
Landau-Kleffner syndrome
Occasional (5-29%)
Encephalocraniocutaneous lipomatosis
Frequent (30-79%)
Osteopathia striata with cranial sclerosis
Occasional (5-29%)
Marchiafava-Bignami disease
Occasional (5-29%)
Nicolaides-Baraitser syndrome
Very frequent (80-99%)
Adult onset basal ganglia disease
Rapid onset dystonia parkinsonism
Frequent (30-79%)
Pitt-Hopkins syndrome
Very frequent (80-99%)
Christianson syndrome
Frequent (30-79%)
Frontotemporal dementia with gene located on 3p11
Hereditary diffuse leukoencephalopathy with axonal spheroids
Lethal ataxia-deafness-optic atrophy
Very frequent (80-99%)
Thiamine transporter-2 deficiency
Frequent (30-79%)
Lower motor neuron degeneration with Paget-like bone disease
Occasional (5-29%)
Short stature and deafness with neutrophil dysfunction and facial dysmorphism syndrome
Frequent (30-79%)
Primary progressive non fluent aphasia
Occasional (5-29%)
Limbic encephalitis with N-methyl-D-aspartate receptor antibodies
Occasional (5-29%)
Quick Facts
- SNOMED CT
- 88052002
- UMLS CUI
- C0026884
- Fully Specified Name
- Mutism (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.