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Ontology Browser
Term:
Parent Terms Term With Siblings Child Terms
eye disease +     
eyelid disease +     
Accommodative esotropia 
Alagille syndrome +  
alpha-mannosidosis +  
anterior segment dysgenesis +  
autoimmune/inflammatory optic neuropathy +   
Axenfeld anomaly 
blepharitis +   
blindness - scoliosis - arachnodactyly syndrome 
chondroectodermal dysplasia with night blindness 
choroidal neovascularization 
coloboma +  
congenital eyelid retraction 
conjunctival disorder +   
corneal disease +   
cryptophthalmia +  
developmental defect of the eye +   
diabetic eye disease +   
dyssegmental dysplasia-glaucoma syndrome 
ectodermal dysplasia-blindness syndrome 
ectropion +   
Ehlers-Danlos syndrome, kyphoscoliotic type 1 
entropion +   
epiblepharon 
essential strabismus 
eye accommodation disease +   
eye adnexa disease +   
eye allergy +  
eye degenerative disorder +   
eye foreign body 
eye hemorrhage +  
eye infectious disorder +   
Eye Injuries, Penetrating 
eye neoplasm +   
eyelid degenerative disorder +  
eyelid disease +   
eyelid neoplasm +  
eyelid seborrheic keratosis 
familial cavitary optic disk anomaly 
fatty acyl-CoA reductase 1 deficiency 
Foster-Kennedy syndrome 
galactosemia +  
galactosialidosis 
Gardner syndrome 
Gaucher disease +   
glaucoma +   
glaucoma-sleep apnea syndrome 
global developmental delay-visual anomalies-progressive cerebellar atrophy-truncal hypotonia syndrome 
GM1 gangliosidosis +  
Graves ophthalmopathy  
hereditary hyperferritinemia with congenital cataracts 
hereditary optic neuropathy +  
herpes zoster with dermatitis of eyelid 
hypertrichosis of eyelid +  
hypopigmentation of eyelid 
hypotrichosis of eyelid 
IgG4-related ophthalmic disorder +  
IRVAN syndrome 
isolated ankyloblepharon filiforme adnatum 
isolated anophthalmia-microphthalmia syndrome +  
isolated Pierre-Robin syndrome 
Ito hypomelanosis 
lacrimal apparatus disease +   
A non-neoplastic or neoplastic disorder that affects the lacrimal apparatus.
lagophthalmos  
lamellar ichthyosis +  
lens disease +   
Lowry-MacLean syndrome 
LTBP2-related ocular dysgenesis +  
Marshall syndrome 
megalocornea-intellectual disability syndrome 
mevalonic aciduria 
microcornea-corectopia-macular hypoplasia syndrome 
microcornea-glaucoma-absent frontal sinuses syndrome 
microphthalmia +  
mucolipidosis type IV 
mucopolysaccharidosis type 1 +  
mucopolysaccharidosis type 6 +  
nail-patella syndrome 
Netherton syndrome 
neuroocular syndrome 
Niemann-Pick disease type A 
Non-accomodative esotropia 
occular toxicity 
ocular cystinosis 
ocular hypertension  
ocular hypotension  
ocular motility disease +   
ocular motor apraxia, Cogan type 
ocular posterior capsular rupture 
ocular sarcoidosis  
ocular siderosis 
ocular vascular disease +   
oculocerebrorenal syndrome 
oculodentodigital dysplasia +  
oculomucocutaneous syndrome 
Opsoclonus-Myoclonus Syndrome 
optic neuritis +   
Peters plus syndrome 
phakomatosis pigmentovascularis +  
piebaldism 
pigment dispersion syndrome  
ptosis +   
Rare genetic eye disease +   
Rare palpebral disease +  
red color blindness 
refractive error +   
retinopathy +   
Retrobulbar Hemorrhage 
rhizomelic chondrodysplasia punctata +  
Rothmund-Thomson syndrome type 2 
scleral disorder +  
SHORT syndrome 
Smith-Lemli-Opitz syndrome 
Sturge-Weber syndrome 
subacute myelo-opticoneuropathy 
syndromic recessive X-linked ichthyosis 
Takayasu arteritis  
telecanthus +  
Tietz syndrome 
tyrosinemia type II 
uveal disorder +   
vitreous body disease +   
X-linked cone dysfunction syndrome with myopia 

Synonyms
Exact Synonyms: disease of lacrimal apparatus ;   disease or disorder of lacrimal apparatus ;   disorder of lacrimal apparatus ;   disorder of lacrimal system ;   lacrimal apparatus disease or disorder ;   lacrimal apparatus disorder ;   lacrimal system disease ;   lacrimal system disorder
Related Synonyms: lachrymal system disorders
Xrefs: DOID:1400 ;   ICD10:H04 ;   ICD9:375 ;   ICD9:375.69 ;   ICD9:375.89 ;   ICD9:375.9 ;   MEDGEN:5994 ;   MESH:D007766 ;   MONDO:0001854 ;   NCI:C26809
External Ontologys: disease_has_location EFO:UBERON:0001750
Definition Sources: NCIT:C26809

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