Overview
Underactivity 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.
X-linked centronuclear myopathy
Huntington's chorea
Frequent (30-79%)
Wilson's disease
Always present (100%)
Merosin deficient congenital muscular dystrophy
Very frequent (80-99%)
Deficiency of tryptophan decarboxylase
Occasional (5-29%)
Westphal-Strumpell syndrome
Always present (100%)
Pena-Shokeir syndrome type I
Very frequent (80-99%)
Danon disease
Monocarboxylate transporter 8 deficiency
Frequent (30-79%)
Autosomal recessive dopa responsive dystonia
Frequent (30-79%)
Spinocerebellar ataxia type 12
Occasional (5-29%)
Severe X-linked mitochondrial encephalomyopathy
Frequent (30-79%)
Dopamine transporter deficiency syndrome
Frequent (30-79%)
Kufor Rakeb syndrome
Frequent (30-79%)
Hereditary hyperekplexia
German syndrome
Very frequent (80-99%)
Congenital disorder of glycosylation type Ip
Occasional (5-29%)
Combined oxidative phosphorylation defect type 2
Always present (100%)
Hepatoencephalopathy due to COXPD1 (combined oxidative phosphorylation defect type 1)
Frequent (30-79%)
HMNDYT2 - hypermanganesemia with dystonia 2
Occasional (5-29%)
Congenital muscular dystrophy with intellectual disability and severe epilepsy
Early-onset prion disease with prominent psychiatric features
Occasional (5-29%)
Ampola syndrome
Merosin-negative congenital muscular dystrophy
Very frequent (80-99%)
Autosomal dominant progressive external ophthalmoplegia
Occasional (5-29%)
Quick Facts
- SNOMED CT
- 43994002
- UMLS CUI
- C0086439
- Fully Specified Name
- Behavior showing reduced motor activity (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.