Overview
Buphthalmos is a finding that may indicate an underlying health condition requiring clinical evaluation.
Associated Conditions
Conditions associated with this symptom based on HPO disease-phenotype annotations.
Atrophia bulborum hereditaria
Frequent (30-79%)
Sturge-Weber sequence
Occasional (5-29%)
Proteus syndrome
Occasional (5-29%)
Persistent hyaloid artery
Lowe syndrome
Frequent (30-79%)
Saethre-Chotzen syndrome
Walker-Warburg congenital muscular dystrophy
Congenital glaucoma
Frequent (30-79%)
Persistent hyperplastic primary vitreous
Charcot-Marie-Tooth disease type 4B2
Occasional (5-29%)
Frank-Ter Haar syndrome
Always present (100%)
Muscle eye brain disease with bilateral multicystic leucodystrophy
Occasional (5-29%)
Congenital labioscrotal agenesis, cerebellar malformation, corneal dystrophy, facial dysmorphism syndrome
Frequent (30-79%)
Colobomatous optic disc, macular atrophy, chorioretinopathy syndrome
Frequent (30-79%)
Microcephaly, facial dysmorphism, ocular anomalies, multiple congenital anomalies syndrome
Frequent (30-79%)
Quick Facts
- SNOMED CT
- 413728006
- UMLS CUI
- C4551507
- Fully Specified Name
- Buphthalmos (finding)
- Associated Conditions
- 15
- 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.