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.
Progressive sclerosing poliodystrophy
African trypanosomiasis
Occasional (5-29%)
Thyrotoxic periodic paralysis
Very frequent (80-99%)
Japanese encephalitis virus disease
Frequent (30-79%)
Variegate porphyria
Poisoning by venomous snake
Occasional (5-29%)
Porphobilinogen synthase deficiency
Adrenoleukodystrophy
Occasional (5-29%)
Tay-Sachs disease, variant AB
Trypanosomiasis
Occasional (5-29%)
Familial hypokalemic periodic paralysis
Very frequent (80-99%)
Chester-type porphyria
Amyotrophic lateral sclerosis
Frequent (30-79%)
Congenital laryngeal adductor paralysis
Acute intermittent porphyria
Type I renal tubular acidosis
Very rare (1-4%)
Encephalocraniocutaneous lipomatosis
Occasional (5-29%)
Porphobilinogen deaminase deficiency
Glioblastoma multiforme
Frequent (30-79%)
Acute poliomyelitis
Frequent (30-79%)
Foodborne botulism
Very frequent (80-99%)
Rift valley fever
Very rare (1-4%)
Inhalational botulism
Very frequent (80-99%)
Primary angiitis of central nervous system
Frequent (30-79%)
Gitelman's syndrome
Very rare (1-4%)
Quick Facts
- SNOMED CT
- 44695005
- UMLS CUI
- C0522224
- Fully Specified Name
- Paralysis (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.