Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Hypoplasia of eyelid |
Finding site |
False |
Eyelid structure |
Inferred relationship |
Some |
2 |
Congenital entropion |
Finding site |
False |
Eyelid structure |
Inferred relationship |
Some |
3 |
Euryblepharon (disorder) |
Finding site |
False |
Eyelid structure |
Inferred relationship |
Some |
2 |
Epiblepharon |
Finding site |
False |
Eyelid structure |
Inferred relationship |
Some |
2 |
Ectopic cilia of eyelid |
Finding site |
False |
Eyelid structure |
Inferred relationship |
Some |
2 |
Coloboma of eyelid |
Finding site |
False |
Eyelid structure |
Inferred relationship |
Some |
2 |
Swan's syndrome II |
Finding site |
False |
Eyelid structure |
Inferred relationship |
Some |
2 |
A decrease in size of opening of the eye, not due to eyelid fusion, but rather lateral displacement of the inner canthi |
Finding site |
False |
Eyelid structure |
Inferred relationship |
Some |
3 |
Ankyloblepharon filiforme adnatum (disorder) |
Finding site |
False |
Eyelid structure |
Inferred relationship |
Some |
3 |
Ohdo syndrome, Maat-Kievit-Brunner type |
Finding site |
False |
Eyelid structure |
Inferred relationship |
Some |
1 |
Partial ablepharon |
Finding site |
False |
Eyelid structure |
Inferred relationship |
Some |
2 |
Congenital structural abnormality of eyelid |
Finding site |
False |
Eyelid structure |
Inferred relationship |
Some |
2 |
Ankyloblepharon |
Finding site |
False |
Eyelid structure |
Inferred relationship |
Some |
3 |
A rare, genetic, multiple congenital anomalies syndrome characterized by the association of a typical facial phenotype with microcephaly associated with congenital hypothyroidism, skeletal involvement (polydactyly, long thumb(s) and long first toe(s), and patellar hypoplasia/agenesis), and some degree of global developmental delay, hypotonia and intellectual disability. Facial features include an immobile mask-like face, severe blepharophimosis and ptosis, tear duct abnormalities, a broad nasal bridge, bulbous nasal tip, small mouth, thin upper lip, hypoplastic teeth and small, low set ears. Renal and genital anomalies, usually cryptorchidism, are often present in affected males. Congenital heart defects and growth delay are variably present. |
Finding site |
False |
Eyelid structure |
Inferred relationship |
Some |
1 |
Ablepharon |
Finding site |
False |
Eyelid structure |
Inferred relationship |
Some |
2 |
Congenital diverticulum of lacrimal canaliculus |
Finding site |
False |
Eyelid structure |
Inferred relationship |
Some |
2 |
Congenital vascular anomaly of eyelid (disorder) |
Finding site |
False |
Eyelid structure |
Inferred relationship |
Some |
3 |
Congenital blepharophimosis of upper eyelid |
Finding site |
False |
Eyelid structure |
Inferred relationship |
Some |
5 |
Congenital vascular anomaly of lower eyelid |
Finding site |
False |
Eyelid structure |
Inferred relationship |
Some |
3 |
Ohdo syndrome, Maat-Kievit-Brunner type |
Finding site |
True |
Eyelid structure |
Inferred relationship |
Some |
2 |
Congenital displacement of punctum lacrimale |
Finding site |
False |
Eyelid structure |
Inferred relationship |
Some |
3 |
A rare, genetic, multiple congenital anomalies syndrome characterized by the association of a typical facial phenotype with microcephaly associated with congenital hypothyroidism, skeletal involvement (polydactyly, long thumb(s) and long first toe(s), and patellar hypoplasia/agenesis), and some degree of global developmental delay, hypotonia and intellectual disability. Facial features include an immobile mask-like face, severe blepharophimosis and ptosis, tear duct abnormalities, a broad nasal bridge, bulbous nasal tip, small mouth, thin upper lip, hypoplastic teeth and small, low set ears. Renal and genital anomalies, usually cryptorchidism, are often present in affected males. Congenital heart defects and growth delay are variably present. |
Finding site |
True |
Eyelid structure |
Inferred relationship |
Some |
2 |
Congenital blepharophimosis of lower eyelid |
Finding site |
False |
Eyelid structure |
Inferred relationship |
Some |
5 |
Congenital vascular anomaly of upper eyelid |
Finding site |
False |
Eyelid structure |
Inferred relationship |
Some |
2 |
Distichiasis |
Finding site |
False |
Eyelid structure |
Inferred relationship |
Some |
3 |
Congenital dysgenetic ptosis |
Finding site |
False |
Eyelid structure |
Inferred relationship |
Some |
3 |
Congenital anomalies of eyelid, lacrimal system and orbit |
Finding site |
True |
Eyelid structure |
Inferred relationship |
Some |
3 |
Ablepharon |
Finding site |
True |
Eyelid structure |
Inferred relationship |
Some |
1 |
Accessory eyelid |
Finding site |
True |
Eyelid structure |
Inferred relationship |
Some |
1 |
Congenital ectropion |
Finding site |
False |
Eyelid structure |
Inferred relationship |
Some |
3 |
Congenital ectropion |
Finding site |
False |
Eyelid structure |
Inferred relationship |
Some |
4 |
Hordeolum externum of upper eyelid |
Finding site |
True |
Eyelid structure |
Inferred relationship |
Some |
2 |
Internal hordeolum of upper eyelid (disorder) |
Finding site |
False |
Eyelid structure |
Inferred relationship |
Some |
1 |
Excision of lash follicles |
Procedure site - Direct (attribute) |
True |
Eyelid structure |
Inferred relationship |
Some |
4 |
Internal hordeolum (disorder) |
Finding site |
True |
Eyelid structure |
Inferred relationship |
Some |
2 |
Internal hordeolum of lower eyelid (disorder) |
Finding site |
True |
Eyelid structure |
Inferred relationship |
Some |
1 |
Hordeolum externum of lower eyelid |
Finding site |
True |
Eyelid structure |
Inferred relationship |
Some |
2 |
Inflammatory lesion of eyelid |
Finding site |
True |
Eyelid structure |
Inferred relationship |
Some |
1 |
Congenital entropion |
Finding site |
True |
Eyelid structure |
Inferred relationship |
Some |
2 |
Eyelid part |
Is a |
True |
Eyelid structure |
Inferred relationship |
Some |
|
Coloboma of eyelid |
Finding site |
False |
Eyelid structure |
Inferred relationship |
Some |
3 |
Entropion from focal conjunctival scarring |
Finding site |
True |
Eyelid structure |
Inferred relationship |
Some |
2 |
Staphylococcal blepharitis |
Finding site |
False |
Eyelid structure |
Inferred relationship |
Some |
2 |
Infective blepharitis |
Finding site |
False |
Eyelid structure |
Inferred relationship |
Some |
2 |
Congenital vascular anomaly of lower eyelid |
Finding site |
False |
Eyelid structure |
Inferred relationship |
Some |
2 |
Specimen from eyelid obtained by biopsy (specimen) |
Specimen source topography |
True |
Eyelid structure |
Inferred relationship |
Some |
1 |
Congenital eyelid retraction is a very rare kinetic eyelid anomaly that can affect the upper or lower eyelid, presents at birth, that in some cases can result in corneal exposure, and that may be associated with accessory levator muscle slips. |
Finding site |
False |
Eyelid structure |
Inferred relationship |
Some |
2 |
Congenital eyelid retraction is a very rare kinetic eyelid anomaly that can affect the upper or lower eyelid, presents at birth, that in some cases can result in corneal exposure, and that may be associated with accessory levator muscle slips. |
Finding site |
False |
Eyelid structure |
Inferred relationship |
Some |
3 |
An extremely rare multiple congenital malformation syndrome characterized by the association of ablepharon, macrostomia, abnormal external ears, syndactyly of the hands and feet, skin findings (such as dry and coarse skin or redundant folds of skin), absent or sparse hair, genital malformations and developmental delay (in 2/3 of cases). Other reported manifestations include malar hypoplasia, absent or hypoplastic nipples, umbilical abnormalities and growth retardation. It is a mainly sporadic disorder, although a few familial cases having been reported, and it displays significant clinical overlap with Fraser syndrome. |
Finding site |
False |
Eyelid structure |
Inferred relationship |
Some |
4 |
A rare congenital abnormality in which the eyelids are absent and skin covers the ocular bulb, which is often microphthalmic. A few cases of complete bilateral cryptophthalmia have been described. |
Finding site |
True |
Eyelid structure |
Inferred relationship |
Some |
1 |
Structure of left eyelid (body structure) |
Is a |
True |
Eyelid structure |
Inferred relationship |
Some |
|
Structure of right eyelid (body structure) |
Is a |
True |
Eyelid structure |
Inferred relationship |
Some |
|
Ectropion of bilateral eyelids (disorder) |
Finding site |
False |
Eyelid structure |
Inferred relationship |
Some |
6 |
Entropion of bilateral eyelids (disorder) |
Finding site |
False |
Eyelid structure |
Inferred relationship |
Some |
6 |
A rare genetic disease characterized by bilateral Duane retraction syndrome type 3 (consisting of severe limitation of abduction, restriction of adduction, retraction of the globe, and narrowing of the palpebral fissure) and congenital myopathy manifesting as mild non-progressive hypotonia without muscular weakness, as well as delayed motor milestones, severe early-onset scoliosis, and short stature. Intelligence is normal. |
Finding site |
False |
Eyelid structure |
Inferred relationship |
Some |
|
Acquired malposition of eyelid (disorder) |
Finding site |
True |
Eyelid structure |
Inferred relationship |
Some |
1 |
Eyelid symptom |
Finding site |
False |
Eyelid structure |
Inferred relationship |
Some |
1 |
A rare multiple congenital anomalies syndrome characterized by nasopalpebral lipomas, bilateral lid coloboma, and telecanthus. |
Finding site |
True |
Eyelid structure |
Inferred relationship |
Some |
2 |
Allergic contact blepharoconjunctivitis (disorder) |
Finding site |
False |
Eyelid structure |
Inferred relationship |
Some |
5 |
Allergic contact blepharoconjunctivitis (disorder) |
Finding site |
False |
Eyelid structure |
Inferred relationship |
Some |
4 |
Congenital malposition of eyelid (disorder) |
Finding site |
True |
Eyelid structure |
Inferred relationship |
Some |
1 |
Hematoma of eyelid (disorder) |
Finding site |
True |
Eyelid structure |
Inferred relationship |
Some |
1 |
Eyelid nystagmus |
Finding site |
True |
Eyelid structure |
Inferred relationship |
Some |
1 |
Repair of entropion with tissue graft (procedure) |
Procedure site - Direct (attribute) |
True |
Eyelid structure |
Inferred relationship |
Some |
2 |
Repair of entropion with tissue graft (procedure) |
Procedure site - Direct (attribute) |
True |
Eyelid structure |
Inferred relationship |
Some |
3 |
Repair of ectropion of eyelid with tissue graft (procedure) |
Procedure site - Direct (attribute) |
True |
Eyelid structure |
Inferred relationship |
Some |
2 |
Repair of ectropion of eyelid with tissue graft (procedure) |
Procedure site - Direct (attribute) |
True |
Eyelid structure |
Inferred relationship |
Some |
3 |
Epidermal inclusion cyst of eyelid |
Finding site |
True |
Eyelid structure |
Inferred relationship |
Some |
1 |
Epithelial inclusion cyst of eyelid (disorder) |
Finding site |
True |
Eyelid structure |
Inferred relationship |
Some |
1 |
Acquired neuromuscular ptosis (disorder) |
Finding site |
True |
Eyelid structure |
Inferred relationship |
Some |
1 |
Entropion of bilateral lower eyelids (disorder) |
Finding site |
False |
Eyelid structure |
Inferred relationship |
Some |
3 |
Entropion of left eyelid (disorder) |
Finding site |
False |
Eyelid structure |
Inferred relationship |
Some |
2 |
Entropion of right lower eyelid |
Finding site |
False |
Eyelid structure |
Inferred relationship |
Some |
2 |
Entropion of left lower eyelid (disorder) |
Finding site |
False |
Eyelid structure |
Inferred relationship |
Some |
2 |
Entropion of right eyelid |
Finding site |
False |
Eyelid structure |
Inferred relationship |
Some |
2 |
Ectropion of left eyelid |
Finding site |
False |
Eyelid structure |
Inferred relationship |
Some |
2 |
Ectropion of right eyelid |
Finding site |
False |
Eyelid structure |
Inferred relationship |
Some |
2 |
Ectropion of left lower eyelid |
Finding site |
False |
Eyelid structure |
Inferred relationship |
Some |
2 |
Ectropion of right lower eyelid |
Finding site |
False |
Eyelid structure |
Inferred relationship |
Some |
2 |
Senile ectropion of right lower eyelid (disorder) |
Finding site |
False |
Eyelid structure |
Inferred relationship |
Some |
2 |
Senile ectropion of bilateral lower eyelids (disorder) |
Finding site |
False |
Eyelid structure |
Inferred relationship |
Some |
3 |
Senile ectropion of left lower eyelid (disorder) |
Finding site |
False |
Eyelid structure |
Inferred relationship |
Some |
2 |
Congenital eyelid retraction is a very rare kinetic eyelid anomaly that can affect the upper or lower eyelid, presents at birth, that in some cases can result in corneal exposure, and that may be associated with accessory levator muscle slips. |
Finding site |
True |
Eyelid structure |
Inferred relationship |
Some |
1 |
An extremely rare multiple congenital malformation syndrome characterized by the association of ablepharon, macrostomia, abnormal external ears, syndactyly of the hands and feet, skin findings (such as dry and coarse skin or redundant folds of skin), absent or sparse hair, genital malformations and developmental delay (in 2/3 of cases). Other reported manifestations include malar hypoplasia, absent or hypoplastic nipples, umbilical abnormalities and growth retardation. It is a mainly sporadic disorder, although a few familial cases having been reported, and it displays significant clinical overlap with Fraser syndrome. |
Finding site |
True |
Eyelid structure |
Inferred relationship |
Some |
1 |
Congenital vascular anomaly of eyelid (disorder) |
Finding site |
True |
Eyelid structure |
Inferred relationship |
Some |
1 |
Congenital nuclear ophthalmoplegia |
Finding site |
False |
Eyelid structure |
Inferred relationship |
Some |
3 |
Sticking of eyelids due to discharge from eyes (finding) |
Finding site |
True |
Eyelid structure |
Inferred relationship |
Some |
1 |
Grafting of skin and fat to eyelid (procedure) |
Procedure site - Direct (attribute) |
True |
Eyelid structure |
Inferred relationship |
Some |
2 |
Senile entropion of lower eyelid (disorder) |
Finding site |
False |
Eyelid structure |
Inferred relationship |
Some |
1 |
Senile entropion of upper eyelid |
Finding site |
False |
Eyelid structure |
Inferred relationship |
Some |
1 |
Senile ectropion of lower eyelid (disorder) |
Finding site |
False |
Eyelid structure |
Inferred relationship |
Some |
1 |
Papilloma of left eyelid (disorder) |
Finding site |
False |
Eyelid structure |
Inferred relationship |
Some |
2 |
Papilloma of right eyelid (disorder) |
Finding site |
False |
Eyelid structure |
Inferred relationship |
Some |
2 |
Squamous cell papilloma of eyelid |
Finding site |
True |
Eyelid structure |
Inferred relationship |
Some |
1 |
Bilateral angular blepharoconjunctivitis of eyes |
Finding site |
False |
Eyelid structure |
Inferred relationship |
Some |
3 |
Angular blepharoconjunctivitis of right eye |
Finding site |
False |
Eyelid structure |
Inferred relationship |
Some |
2 |
A decrease in size of opening of the eye, not due to eyelid fusion, but rather lateral displacement of the inner canthi |
Finding site |
False |
Eyelid structure |
Inferred relationship |
Some |
2 |
Splinter in eyelid |
Finding site |
True |
Eyelid structure |
Inferred relationship |
Some |
1 |
A rare, genetic, syndromic intellectual disability disorder characterized by congenital, external, nuclear ophthalmoplegia, lingua scrotalis, progressive chorioretinal sclerosis and intellectual disability. Bilateral ptosis, bilateral facial weakness, Parinaud's syndrome, convergence paresis and myopia may be associated. There have been no further descriptions in the literature since 1975. |
Finding site |
True |
Eyelid structure |
Inferred relationship |
Some |
4 |
Harlequin ichthyosis |
Finding site |
True |
Eyelid structure |
Inferred relationship |
Some |
3 |
Blepharophimosis syndrome |
Finding site |
False |
Eyelid structure |
Inferred relationship |
Some |
2 |