Rare diseases · Sign or symptom
Visual field defect
Partial loss of field of vision
HP:0001123
Rare diseases that can present with this33
Very common80–99%
4Common30–79%
12- Acute zonal occult outer retinopathy
- Adult-onset foveomacular vitelliform dystrophy
- Autosomal recessive spastic paraplegia type 74
- Combined oxidative phosphorylation defect type 7
- Familial cerebral saccular aneurysm
- Fatty acid hydroxylase-associated neurodegeneration
- Functioning gonadotropic adenoma
- Maternal uniparental disomy of chromosome 4 syndrome
- Pituicytoma
- Sneddon syndrome
- Sturge-Weber syndrome
- X-linked adrenoleukodystrophy
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, and Orphanet separately records 1 disease where this sign is specifically absent. A sign on this page is a conversation to have with a clinician, not a conclusion.
Part of the broader category
Also called: Visual field defects
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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.