raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:199323

Endophthalmitis

Type
Disease
Group
Disorder
Status
active

A rare ophthalmic disorder characterized by inflammation involving the vitreous and/or aqueous humors, usually due to bacterial or fungal infection. It may arise endogenously from hematogenous spread of the infectious agent, or exogenously after direct inoculation, and can take an acute or chronic course. Clinical signs and symptoms include progressive vitritis, hypopyon, reduced or blurred vision, red eye, pain, and lid swelling. The condition may be complicated by panophthalmitis, corneal infiltration and perforation, affection of orbital structures, and phthisis bulbi.

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enEndophthalmitis
frEndophtalmie
deEndophthalmitis
esEndoftalmitis
itEndoftalmite
nlEndoftalmitis
ptEndoftalmite
plZapalenie wnętrza gałki ocznej
csEndoftalmitida
ukЕндофтальміт
zh眼内炎
trEndoftalmit

Definition in:

2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
ICD-10H44.0BTNTspecificvalidated
ICD-10H44.1BTNTspecificvalidated
ICD-119C21Especificvalidated
MONDO0016047Evalidated
MeSHD009877Evalidated
UMLSC0014236Evalidated
MedDRA10014801Evalidated

E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.

3

Classification

Preferential parent (Orphanet linearisation):

Parents in the classifications (1):

Children (2):

4

Genes

0 direct

Orphanet records no gene directly on this code.

5

Prevalence and incidence

0 records

No prevalence record in this release.

6

HPO phenotypes

Orphanet has no HPO annotation for this code in this release.

7

Sources for this card