Rare diseases · Sign or symptom
Oral-pharyngeal dysphagia
HP:0200136
Rare diseases that can present with this17
Common30–79%
12- 17p11.2microduplication syndrome
- Alternating hemiplegia of childhood
- Cleft lip/palate
- Cleft velum
- Gabriele-de Vries syndrome
- Helsmoortel-Van der Aa syndrome
- Laryngeal neuroendocrine tumor
- Oculopharyngodistal myopathy
- Pontocerebellar hypoplasia type 2
- Severe Canavan disease
- Stevens-Johnson syndrome/toxic epidermal necrolysis spectrum
- X-linked intellectual disability-global development delay-facial dysmorphism-sacral caudal remnant syndrome
The range is how often this sign appears among people diagnosed with each disease — it is not a probability of having any of them. Many of these signs also occur in common, non-rare conditions. A sign on this page is a conversation to have with a clinician, not a conclusion.
Part of the broader category
Also called: Oral pharyngeal dysphagia · Oropharyngeal dysphagia
Oral-pharyngeal dysphagia
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Start free with EleplanThis page uses the Human Phenotype Ontology (2026-06-23) — Human Phenotype Ontology Consortium, hpo.jax.org. Disease associations from Orphanet (INSERM), CC BY 4.0. Content is educational and is not medical advice.