Overview
Difficulty standing 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.
Arachnoid cyst
Occasional (5-29%)
Vitamin D-dependent rickets, type 1
Vitamin D-dependent rickets, type 2
Dyggve-Melchior-Clausen syndrome
Occasional (5-29%)
Landau-Kleffner syndrome
Occasional (5-29%)
Autosomal recessive hypophosphatemic bone disease
Vitamin D-dependent rickets type II with alopecia
Snyder-Robinson syndrome
Occasional (5-29%)
Progressive epilepsy with mental retardation
Frequent (30-79%)
Hereditary motor and sensory neuropathy Okinawa type
Frequent (30-79%)
Spinocerebellar ataxia type 29
Always present (100%)
Autosomal recessive spastic paraplegia type 57
Always present (100%)
Hereditary hypophosphatemic rickets with hypercalciuria
Superficial siderosis of central nervous system
Occasional (5-29%)
Distal myotilinopathy
Frequent (30-79%)
Autosomal recessive spastic paraplegia type 24
Proximal spinal muscular atrophy
Occasional (5-29%)
Early-onset progressive encephalopathy, spastic ataxia, distal spinal muscular atrophy syndrome
Frequent (30-79%)
Kyphoscoliosis, lateral tongue atrophy, hereditary spastic paraplegia syndrome
Frequent (30-79%)
Combined oxidative phosphorylation defect type 26
Frequent (30-79%)
Neurodevelopmental delay, seizures, ophthalmic anomalies, osteopenia, cerebellar atrophy syndrome
Frequent (30-79%)
FAR1 deficiency
Occasional (5-29%)
WARS2-related combined oxidative phosphorylation defect
Occasional (5-29%)
Limb girdle muscular dystrophy type R24
Occasional (5-29%)
Quick Facts
- SNOMED CT
- 249902000
- UMLS CUI
- C0241237
- Fully Specified Name
- Difficulty standing (finding)
- Associated Conditions
- 24
- 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.