Overview
Hyperreflexia 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.
Xeroderma pigmentosum, group B
Pigmentary pallidal degeneration
Occasional (5-29%)
Typhoid fever
Frequent (30-79%)
Stiff-man syndrome
Frequent (30-79%)
Classical phenylketonuria
Lesch-Nyhan syndrome
Acute neuronopathic Gaucher's disease
Methylcrotonyl-CoA carboxylase deficiency
Atrophia bulborum hereditaria
Occasional (5-29%)
Cross syndrome
Frequent (30-79%)
Sturge-Weber sequence
Frequent (30-79%)
Cockayne syndrome
Occasional (5-29%)
Sandhoff disease
Always present (100%)
Metachromatic leukodystrophy, adult type
Megaloblastic anemia due to impaired absorption of folate
Occasional (5-29%)
Orthostatic hypotension
Leigh's disease
Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome
Very frequent (80-99%)
Fanconi pancytopenia syndrome
Occasional (5-29%)
Ectodermal dysplasia-ocular malformation syndrome
Frequent (30-79%)
Glutamate-cysteine ligase deficiency
Occasional (5-29%)
Oculodentodigital syndrome
Frequent (30-79%)
Sialidosis
Metachromatic leukodystrophy, congenital type
Metachromatic leukodystrophy, juvenile type
Quick Facts
- SNOMED CT
- 86854008
- UMLS CUI
- C0151889
- Fully Specified Name
- Hyperreflexia (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.