Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Epiblepharon |
Is a |
True |
Congenital structural abnormality of eyelid |
Inferred relationship |
Some |
|
Congenital ankyloblepharon |
Is a |
True |
Congenital structural abnormality of eyelid |
Inferred relationship |
Some |
|
Congenital distichiasis |
Is a |
False |
Congenital structural abnormality of eyelid |
Inferred relationship |
Some |
|
Congenital ptosis (disorder) |
Is a |
True |
Congenital structural abnormality of eyelid |
Inferred relationship |
Some |
|
Ablepharon |
Is a |
True |
Congenital structural abnormality of eyelid |
Inferred relationship |
Some |
|
Congenital entropion |
Is a |
True |
Congenital structural abnormality of eyelid |
Inferred relationship |
Some |
|
Accessory eyelid |
Is a |
True |
Congenital structural abnormality of eyelid |
Inferred relationship |
Some |
|
Congenital ectropion |
Is a |
True |
Congenital structural abnormality of eyelid |
Inferred relationship |
Some |
|
Globe of eye vestigial |
Is a |
False |
Congenital structural abnormality of eyelid |
Inferred relationship |
Some |
|
Congenital absence of eyelash |
Is a |
False |
Congenital structural abnormality of eyelid |
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 |
True |
Congenital structural abnormality of eyelid |
Inferred relationship |
Some |
|
Congenital abnormal vertical shortness of eyelids |
Is a |
True |
Congenital structural abnormality of eyelid |
Inferred relationship |
Some |
|
Coloboma of eyelid |
Is a |
True |
Congenital structural abnormality of eyelid |
Inferred relationship |
Some |
|
Distichiasis |
Is a |
False |
Congenital structural abnormality of eyelid |
Inferred relationship |
Some |
|
Macropalpebral fissure |
Is a |
True |
Congenital structural abnormality of eyelid |
Inferred relationship |
Some |
|
Ectopic cilia of eyelid |
Is a |
True |
Congenital structural abnormality of eyelid |
Inferred relationship |
Some |
|
Congenitally small punctum lacrimale |
Is a |
False |
Congenital structural abnormality of eyelid |
Inferred relationship |
Some |
|
Congenital displacement of punctum lacrimale |
Is a |
False |
Congenital structural abnormality of eyelid |
Inferred relationship |
Some |
|
Congenital diverticulum of lacrimal canaliculus |
Is a |
True |
Congenital structural abnormality of eyelid |
Inferred relationship |
Some |
|
Congenital anomaly of third eyelid |
Is a |
False |
Congenital structural abnormality of eyelid |
Inferred relationship |
Some |
|
Eyelid vascular anomalies |
Is a |
False |
Congenital structural abnormality of eyelid |
Inferred relationship |
Some |
|
Agenesis of cilia |
Is a |
False |
Congenital structural abnormality of eyelid |
Inferred relationship |
Some |
|
Hypoplasia of eyelid |
Is a |
True |
Congenital structural abnormality of eyelid |
Inferred relationship |
Some |
|
Congenital eyelid deformity NOS |
Is a |
False |
Congenital structural abnormality of eyelid |
Inferred relationship |
Some |
|
Other specified congenital eyelid anomalies |
Is a |
False |
Congenital structural abnormality of eyelid |
Inferred relationship |
Some |
|
Other specified congenital eyelid anomalies NOS |
Is a |
False |
Congenital structural abnormality of eyelid |
Inferred relationship |
Some |
|
[X]Other congenital malformations of eyelid |
Is a |
False |
Congenital structural abnormality of eyelid |
Inferred relationship |
Some |
|
Agenesis of punctum lacrimale |
Is a |
False |
Congenital structural abnormality of eyelid |
Inferred relationship |
Some |
|
Congenital obstruction of lacrimal canal |
Is a |
False |
Congenital structural abnormality of eyelid |
Inferred relationship |
Some |
|
Ankyloblepharon |
Is a |
False |
Congenital structural abnormality of eyelid |
Inferred relationship |
Some |
|
Cryptophthalmos (disorder) |
Is a |
True |
Congenital structural abnormality of eyelid |
Inferred relationship |
Some |
|
Congenital tarsal kink (disorder) |
Is a |
True |
Congenital structural abnormality of eyelid |
Inferred relationship |
Some |
|
Euryblepharon (disorder) |
Is a |
True |
Congenital structural abnormality of eyelid |
Inferred relationship |
Some |
|
Congenital obstruction of lacrimal canal |
Is a |
True |
Congenital structural abnormality of eyelid |
Inferred relationship |
Some |
|
Supernumerary canaliculus (disorder) |
Is a |
False |
Congenital structural abnormality of eyelid |
Inferred relationship |
Some |
|
Dysgenesis of lacrimal punctum (disorder) |
Is a |
False |
Congenital structural abnormality of eyelid |
Inferred relationship |
Some |
|
Supernumerary lacrimal punctum |
Is a |
False |
Congenital structural abnormality of eyelid |
Inferred relationship |
Some |
|
Imperforate lacrimal punctum |
Is a |
False |
Congenital structural abnormality of eyelid |
Inferred relationship |
Some |
|
Congenital vascular anomaly of eyelid (disorder) |
Is a |
True |
Congenital structural abnormality of eyelid |
Inferred relationship |
Some |
|
Distichiasis |
Is a |
False |
Congenital structural abnormality of eyelid |
Inferred relationship |
Some |
|
Congenital anomalies of eyelid, lacrimal system and orbit |
Is a |
True |
Congenital structural abnormality of eyelid |
Inferred relationship |
Some |
|
Dysgenesis of lacrimal punctum (disorder) |
Is a |
True |
Congenital structural abnormality of eyelid |
Inferred relationship |
Some |
|
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. |
Is a |
True |
Congenital structural abnormality of eyelid |
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 |
Congenital structural abnormality of eyelid |
Inferred relationship |
Some |
|
Dacryocystitis and osteopoikilosis syndrome (disorder) |
Is a |
True |
Congenital structural abnormality of eyelid |
Inferred relationship |
Some |
|
A very rare dysmorphic disorder characterized by hypoplasia and coloboma of the alar cartilages and telecanthus described in 2 sisters. No new cases with similar features have been reported since 1976. |
Is a |
True |
Congenital structural abnormality of eyelid |
Inferred relationship |
Some |
|
A rare malformation syndrome characterized by the association of toe syndactyly, facial dysmorphism including telecanthus (abnormal distance between the eyes) and a broad nasal tip, urogenital malformations and anal atresia. |
Is a |
True |
Congenital structural abnormality of eyelid |
Inferred relationship |
Some |
|
Telecanthus-hypertelorism-strabismus-pes cavus syndrome is characterized by telecanthus, hypertelorism, strabismus, pes cavus and other variable anomalies. It has been described in a father and his son. The son also had hypospadias, bilateral inguinal hernia, clinodactyly and camptodactyly of the fingers, and radiographic findings including flared metaphyses of the long bones and osteopenia. |
Is a |
True |
Congenital structural abnormality of eyelid |
Inferred relationship |
Some |
|
Familial isolated trichomegaly is a rare genetic hair anomaly characterized by a prolonged anagen phase of the eyelash hairs, leading to extreme eyelash growth that may result in corneal irritation. Increased growth of hair on other parts of the face (eyebrows, cheeks, forehead) and/or the body (chest, arms, legs) may be associated. |
Is a |
True |
Congenital structural abnormality of eyelid |
Inferred relationship |
Some |
|
A rare, genetic multiple congenital anomalies syndrome characterized by atrioventricular septal defects and blepharophimosis, in addition to radial (e.g. aplastic radius, shortened ulna, fifth finger clinodactyly, absent first metacarpal and thumb) and anal (e.g. imperforate or anteriorly place anus, rectovaginal fistula) defects. |
Is a |
False |
Congenital structural abnormality of eyelid |
Inferred relationship |
Some |
|
A rare, genetic multiple congenital anomalies/dysmorphic syndrome characterized by congenital microcephaly, severe epilepsy with hypsarrhythmia, adducted thumbs, abnormal genitalia, and normal thyroid function. Hypotonia, moderate to severe psychomotor delay, and characteristic facial dysmorphism (including round face with prominent cheeks, blepharophimosis, large, bulbous nose with wide alae nasi, posteriorly rotated ears with dysplastic conchae, narrow mouth, cleft palate, and mild micrognathia) are additional characteristic features. |
Is a |
False |
Congenital structural abnormality of eyelid |
Inferred relationship |
Some |
|
Harlequin ichthyosis |
Is a |
False |
Congenital structural abnormality of eyelid |
Inferred relationship |
Some |
|
Congenital nuclear ophthalmoplegia |
Is a |
True |
Congenital structural abnormality of eyelid |
Inferred relationship |
Some |
|
Ascher's syndrome |
Is a |
False |
Congenital structural abnormality of eyelid |
Inferred relationship |
Some |
|
Congenital structural abnormality of right eyelid |
Is a |
True |
Congenital structural abnormality of eyelid |
Inferred relationship |
Some |
|
Congenital structural abnormality of left eyelid (disorder) |
Is a |
True |
Congenital structural abnormality of eyelid |
Inferred relationship |
Some |
|
Dystopia canthorum (disorder) |
Is a |
True |
Congenital structural abnormality of eyelid |
Inferred relationship |
Some |
|
Congenital malposition of eyelid (disorder) |
Is a |
True |
Congenital structural abnormality of eyelid |
Inferred relationship |
Some |
|
Congenital melanocytic naevus of skin of lower eyelid |
Is a |
True |
Congenital structural abnormality of eyelid |
Inferred relationship |
Some |
|
Congenital melanocytic nevus of skin of upper eyelid (disorder) |
Is a |
True |
Congenital structural abnormality of eyelid |
Inferred relationship |
Some |
|