Rare diseases · Sign or symptom
Progressive extrapyramidal movement disorder
HP:0007153
Rare diseases that can present with this8
Common30–79%
6- 3-methylglutaconic aciduria-neonatal cataract-neurologic involvement-congenital neutropenia syndrome
- Fatty acid hydroxylase-associated neurodegeneration
- Guanidinoacetate methyltransferase deficiency
- PLA2G6-related neurodegeneration, adult-onset
- Proximal myopathy with extrapyramidal signs
- RARS-related autosomal recessive hypomyelinating leukodystrophy
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
Progressive extrapyramidal movement…
Tracking symptoms like this for someone? Eleplan keeps symptoms, diagnoses, medications and every specialist in one plan.
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.