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Ontology Browser
Term:
isolated ankyloblepharon filiforme adnatum (EFO:MONDO:0019626)
Annotations: Rat: (0) Mouse: (0) Human: (0) Chinchilla: (0) Bonobo: (0) Dog: (0) Squirrel: (0) Pig: (0) Naked Mole-rat: (0) Green Monkey: (0)
Parent Terms Term With Siblings Child Terms
eye disease +     
Accommodative esotropia  
Alagille syndrome +  
alpha-mannosidosis +  
anterior segment dysgenesis +  
autoimmune/inflammatory optic neuropathy +   
Axenfeld anomaly 
blindness - scoliosis - arachnodactyly syndrome 
chondroectodermal dysplasia with night blindness 
choroidal neovascularization 
coloboma +  
Conjunctival Disorder +  
corneal disease +   
developmental defect of the eye +   
diabetic eye disease +   
dyssegmental dysplasia-glaucoma syndrome 
ectodermal dysplasia-blindness syndrome 
Ehlers-Danlos syndrome, kyphoscoliotic type 1 
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 disease +   
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 +  
IgG4-related ophthalmic disorder +  
IRVAN syndrome 
isolated ankyloblepharon filiforme adnatum 
Isolated ankyloblepharon filiforme adnatum (AFA) is characterized by the presence of single or multiple thin bands of connective tissue between the upper and lower eyelids, preventing full opening of the eye. Several cases have been reported. It can occur sporadically or following an autosomal dominant transmission pattern. In some cases, AFA can be associated with other disorders, such as trisomy 18. The bands should be removed to avoid amblyopia and this can easily be performed in the neonatal period by cutting with tissue scissors.
isolated anophthalmia-microphthalmia syndrome +  
isolated Pierre-Robin syndrome 
Ito hypomelanosis 
lacrimal apparatus disease +   
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 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 +   
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  
Tietz syndrome 
tyrosinemia type II 
uveal disorder +   
vitreous body disease +   
X-linked cone dysfunction syndrome with myopia 

Synonyms
Alternate IDs: MONDO:0019626
Xrefs: GARD:19168 ;   MEDGEN:227001 ;   ORDO:91397 ;   UMLS:C1302999 ;   icd11.foundation:1002292151
Definition Sources: Orphanet:91397

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