Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Deformity of eyelid due to infective dermatitis of eyelid |
Is a |
True |
Deformity of eyelid (disorder) |
Inferred relationship |
Some |
|
Congenital abnormal vertical shortness of eyelids |
Is a |
True |
Deformity of eyelid (disorder) |
Inferred relationship |
Some |
|
Acquired scleral show due to eyelid deformity (finding) |
Due to |
True |
Deformity of eyelid (disorder) |
Inferred relationship |
Some |
1 |
Eversion of lacrimal punctum |
Is a |
False |
Deformity of eyelid (disorder) |
Inferred relationship |
Some |
|
Ectropion |
Is a |
True |
Deformity of eyelid (disorder) |
Inferred relationship |
Some |
|
Lower eyelid entropion |
Is a |
False |
Deformity of eyelid (disorder) |
Inferred relationship |
Some |
|
Upper eyelid entropion |
Is a |
False |
Deformity of eyelid (disorder) |
Inferred relationship |
Some |
|
Nasal canthal entropion |
Is a |
False |
Deformity of eyelid (disorder) |
Inferred relationship |
Some |
|
Congenital entropion |
Is a |
False |
Deformity of eyelid (disorder) |
Inferred relationship |
Some |
|
Trichomegaly-retina pigmentary degeneration-dwarfism syndrome, also known as Oliver-McFarlane syndrome, is an extremely rare genetic disorder characterized by hair abnormalities, severe chorioretinal atrophy, hypopituitarism, short stature, and intellectual disability. |
Is a |
True |
Deformity of eyelid (disorder) |
Inferred relationship |
Some |
|
Entropion of bilateral eyelids (disorder) |
Is a |
False |
Deformity of eyelid (disorder) |
Inferred relationship |
Some |
|
Tear trough deformity of lower eyelid (disorder) |
Is a |
True |
Deformity of eyelid (disorder) |
Inferred relationship |
Some |
|
Entropion of left eyelid (disorder) |
Is a |
False |
Deformity of eyelid (disorder) |
Inferred relationship |
Some |
|
Entropion of right eyelid |
Is a |
False |
Deformity of eyelid (disorder) |
Inferred relationship |
Some |
|
Entropion |
Is a |
True |
Deformity of eyelid (disorder) |
Inferred relationship |
Some |
|
A decrease in size of opening of the eye, not due to eyelid fusion, but rather lateral displacement of the inner canthi |
Is a |
False |
Deformity of eyelid (disorder) |
Inferred relationship |
Some |
|
Blepharophimosis syndrome |
Is a |
False |
Deformity of eyelid (disorder) |
Inferred relationship |
Some |
|
Blepharophimosis, intellectual disability syndrome (disorder) |
Is a |
True |
Deformity of eyelid (disorder) |
Inferred relationship |
Some |
|
A rare disorder of the ocular adnexa characterized by an extended phenotype of blepharophimosis, ptosis, epicanthus inversus and telecanthus syndrome (BPES). When BPES is caused by a microdeletion encompassing other genes in addition to the causative gene FOXL2, the patient has additional features including intellectual disability, external genital anomaly, spastic diplegia, and speech delay. Acquired microcephaly can also be observed. |
Is a |
False |
Deformity of eyelid (disorder) |
Inferred relationship |
Some |
|
A rare ophthalmic disorder characterized by blepharophimosis, ptosis, epicanthus inversus, and telecanthus, that can appear associated with (type 1) or without primary ovarian insufficiency (POI; type 2). |
Is a |
True |
Deformity of eyelid (disorder) |
Inferred relationship |
Some |
|