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.
Jakob-Creutzfeldt disease
Gestational rubella syndrome
Frequent (30-79%)
Senter syndrome
Frequent (30-79%)
Weill-Marchesani syndrome
Occasional (5-29%)
Pigmentary pallidal degeneration
Very frequent (80-99%)
11p partial monosomy syndrome
Frequent (30-79%)
Listeriosis
Very rare (1-4%)
Hypertyrosinemia, Richner-Hanhart type
Occasional (5-29%)
Tyrosinase-negative oculocutaneous albinism
Septo-optic dysplasia sequence
Very frequent (80-99%)
Metaphyseal chondrodysplasia, McKusick type
Very frequent (80-99%)
Hallermann-Streiff syndrome
Frequent (30-79%)
Biotinidase deficiency
Hermansky-Pudlak syndrome
Occasional (5-29%)
Killian-Teschler-Nicola syndrome
Frequent (30-79%)
Coffin-Siris syndrome
Friedreich's ataxia
Occasional (5-29%)
Fibrous dysplasia of bone
Very rare (1-4%)
Brown oculocutaneous albinism
Familial hypoalphalipoproteinemia
Mucopolysaccharidosis, MPS-III-D
Frequent (30-79%)
Schinzel-Giedion syndrome
Frequent (30-79%)
Marfan's syndrome
Frequent (30-79%)
Sturge-Weber sequence
Occasional (5-29%)
Progressive sclerosing poliodystrophy
Quick Facts
- SNOMED CT
- 7973008
- UMLS CUI
- C3665386
- Fully Specified Name
- Abnormal vision (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.