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.
Fisher's syndrome
Very frequent (80-99%)
Triglyceride storage disease with ichthyosis
Frequent (30-79%)
Progressive sclerosing poliodystrophy
Frequent (30-79%)
Cockayne syndrome
Occasional (5-29%)
Glutaric aciduria, type 2
Occasional (5-29%)
Tonic pupillary reaction
Frequent (30-79%)
Arteriohepatic dysplasia
Charcot-Marie-Tooth disease, type IA
Charcot-Marie-Tooth disease, type IB
Frequent (30-79%)
Sarcotubular myopathy
Roussy-Lévy syndrome
Frequent (30-79%)
X-linked centronuclear myopathy
Frequent (30-79%)
Infantile neuroaxonal dystrophy
Werdnig-Hoffmann disease
Choreoacanthocytosis
Frequent (30-79%)
Gerstmann-Straussler-Scheinker syndrome
Frequent (30-79%)
Dihydrouracil dehydrogenase (NADP^+^) deficiency
Occasional (5-29%)
POEMS syndrome
Frequent (30-79%)
Lowe syndrome
Very frequent (80-99%)
Marinesco-Sjogren syndrome
Occasional (5-29%)
Zellweger syndrome
Gonadal dysgenesis with auditory dysfunction, autosomal recessive inheritance
Occasional (5-29%)
Syringomyelia
Déjérine-Sottas disease
Always present (100%)
Fukuyama congenital muscular dystrophy
Quick Facts
- SNOMED CT
- 349006
- UMLS CUI
- C0278124
- Fully Specified Name
- Absent tendon reflex (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.