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.
Childhood type dermatomyositis
Occasional (5-29%)
Pigmentary pallidal degeneration
Frequent (30-79%)
Friedreich's ataxia
Very frequent (80-99%)
Lesch-Nyhan syndrome
Mucopolysaccharidosis, MPS-III-D
Frequent (30-79%)
Niemann-Pick disease, type D
Postencephalitic parkinsonism
Occasional (5-29%)
Echinococcus multilocularis infection
Very rare (1-4%)
Progressive multifocal leukoencephalopathy
Frequent (30-79%)
Sandhoff disease
Cystathionine beta-synthase deficiency
Always present (100%)
Metachromatic leukodystrophy, adult type
Frequent (30-79%)
Chorea acanthocytosis syndrome
Occasional (5-29%)
Orthostatic hypotension
Progressive supranuclear ophthalmoplegia
Frequent (30-79%)
Leigh's disease
Post poliomyelitis syndrome
Occasional (5-29%)
Ectodermal dysplasia-ocular malformation syndrome
Frequent (30-79%)
Hypogonadotropic hypogonadism
Occasional (5-29%)
Glutamate-cysteine ligase deficiency
Occasional (5-29%)
Oculodentodigital syndrome
Frequent (30-79%)
Glutathione synthase deficiency with 5-oxoprolinuria
Metachromatic leukodystrophy, congenital type
Frequent (30-79%)
Langer-Giedion syndrome
Occasional (5-29%)
Globoid cell leukodystrophy, late-onset
Occasional (5-29%)
Quick Facts
- SNOMED CT
- 8011004
- UMLS CUI
- C0013362
- Fully Specified Name
- Dysarthria (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.