Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Internasal dysostosis |
Is a |
True |
Congenital anomaly of face (disorder) |
Inferred relationship |
Some |
|
A genetically heterogeneous autosomal recessive syndrome characterised by the triad of amelogenesis imperfect, infantile onset epilepsy, intellectual disability with or without regression and dementia. |
Is a |
False |
Congenital anomaly of face (disorder) |
Inferred relationship |
Some |
|
Macrogenia |
Is a |
False |
Congenital anomaly of face (disorder) |
Inferred relationship |
Some |
|
Congenital anomaly of lip |
Is a |
True |
Congenital anomaly of face (disorder) |
Inferred relationship |
Some |
|
Cerebrofacial dysplasia |
Is a |
True |
Congenital anomaly of face (disorder) |
Inferred relationship |
Some |
|
Congenital anosmia |
Is a |
False |
Congenital anomaly of face (disorder) |
Inferred relationship |
Some |
|
Congenital absence of nose |
Is a |
False |
Congenital anomaly of face (disorder) |
Inferred relationship |
Some |
|
Congenital distichiasis |
Is a |
False |
Congenital anomaly of face (disorder) |
Inferred relationship |
Some |
|
Congenital abnormality of oral cavity |
Is a |
False |
Congenital anomaly of face (disorder) |
Inferred relationship |
Some |
|
Facial asymmetry |
Is a |
False |
Congenital anomaly of face (disorder) |
Inferred relationship |
Some |
|
Congenital anomaly of face bones |
Is a |
True |
Congenital anomaly of face (disorder) |
Inferred relationship |
Some |
|
Gingival cyst of newborn |
Is a |
False |
Congenital anomaly of face (disorder) |
Inferred relationship |
Some |
|
Congenital atresia of nares |
Is a |
False |
Congenital anomaly of face (disorder) |
Inferred relationship |
Some |
|
Periodontal Ehlers-Danlos syndrome (disorder) |
Is a |
False |
Congenital anomaly of face (disorder) |
Inferred relationship |
Some |
|
Cherubism |
Is a |
False |
Congenital anomaly of face (disorder) |
Inferred relationship |
Some |
|
Nasal glial heterotopia |
Is a |
False |
Congenital anomaly of face (disorder) |
Inferred relationship |
Some |
|
Increased superior-inferior overlap of the maxillary central incisors over the mandibular central incisors relative to the incisal ridges. |
Is a |
False |
Congenital anomaly of face (disorder) |
Inferred relationship |
Some |
|
Congenital absence of eyelash |
Is a |
False |
Congenital anomaly of face (disorder) |
Inferred relationship |
Some |
|
Nasal encephalocele |
Is a |
False |
Congenital anomaly of face (disorder) |
Inferred relationship |
Some |
|
Horizontal overbite |
Is a |
False |
Congenital anomaly of face (disorder) |
Inferred relationship |
Some |
|
Syphilitic saddle nose |
Is a |
False |
Congenital anomaly of face (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 |
Congenital anomaly of face (disorder) |
Inferred relationship |
Some |
|
Distichiasis |
Is a |
False |
Congenital anomaly of face (disorder) |
Inferred relationship |
Some |
|
Congenital anomaly of jaw |
Is a |
False |
Congenital anomaly of face (disorder) |
Inferred relationship |
Some |
|
Ectopic cilia of eyelid |
Is a |
False |
Congenital anomaly of face (disorder) |
Inferred relationship |
Some |
|
Fistula of congenital auricle |
Is a |
False |
Congenital anomaly of face (disorder) |
Inferred relationship |
Some |
|
Deformity of nasal sinus wall |
Is a |
False |
Congenital anomaly of face (disorder) |
Inferred relationship |
Some |
|
Congenital perforation of the nasal sinus wall |
Is a |
False |
Congenital anomaly of face (disorder) |
Inferred relationship |
Some |
|
Congenital deformity of face (disorder) |
Is a |
True |
Congenital anomaly of face (disorder) |
Inferred relationship |
Some |
|
Preauricular sinus |
Is a |
False |
Congenital anomaly of face (disorder) |
Inferred relationship |
Some |
|
Preauricular fistula |
Is a |
True |
Congenital anomaly of face (disorder) |
Inferred relationship |
Some |
|
Mandibuloacral dysostosis |
Is a |
False |
Congenital anomaly of face (disorder) |
Inferred relationship |
Some |
|
Buccal bifurcation cyst |
Is a |
False |
Congenital anomaly of face (disorder) |
Inferred relationship |
Some |
|
Saddle nose |
Is a |
False |
Congenital anomaly of face (disorder) |
Inferred relationship |
Some |
|
Congenital anomaly of nose |
Is a |
True |
Congenital anomaly of face (disorder) |
Inferred relationship |
Some |
|
Congenital anomaly of nasal sinuses |
Is a |
False |
Congenital anomaly of face (disorder) |
Inferred relationship |
Some |
|
Microstomia |
Is a |
False |
Congenital anomaly of face (disorder) |
Inferred relationship |
Some |
|
Congenital macrostomia |
Is a |
True |
Congenital anomaly of face (disorder) |
Inferred relationship |
Some |
|
Congenital anomaly of teeth |
Is a |
False |
Congenital anomaly of face (disorder) |
Inferred relationship |
Some |
|
museau court congénital |
Is a |
False |
Congenital anomaly of face (disorder) |
Inferred relationship |
Some |
|
Crouzon disease is characterised by craniosynostosis and facial hypoplasia. |
Is a |
False |
Congenital anomaly of face (disorder) |
Inferred relationship |
Some |
|
Congenital absence of chin |
Is a |
False |
Congenital anomaly of face (disorder) |
Inferred relationship |
Some |
|
Congenital malformation of the eyebrow |
Is a |
True |
Congenital anomaly of face (disorder) |
Inferred relationship |
Some |
|
Congenital structural abnormality of eyelid |
Is a |
True |
Congenital anomaly of face (disorder) |
Inferred relationship |
Some |
|
Weissenbacher-Zweymuller syndrome |
Is a |
False |
Congenital anomaly of face (disorder) |
Inferred relationship |
Some |
|
Potter's facies |
Is a |
True |
Congenital anomaly of face (disorder) |
Inferred relationship |
Some |
|
Macrogenia |
Is a |
False |
Congenital anomaly of face (disorder) |
Inferred relationship |
Some |
|
Ear, face and neck congenital anomalies |
Is a |
True |
Congenital anomaly of face (disorder) |
Inferred relationship |
Some |
|
Fordyce spots of buccal mucosa (disorder) |
Is a |
False |
Congenital anomaly of face (disorder) |
Inferred relationship |
Some |
|
Multiple malformation syndrome with facial defects as major feature |
Is a |
True |
Congenital anomaly of face (disorder) |
Inferred relationship |
Some |
|
Arteriovenous malformation of face (disorder) |
Is a |
True |
Congenital anomaly of face (disorder) |
Inferred relationship |
Some |
|
Fronto-malar faciosynostosis |
Is a |
True |
Congenital anomaly of face (disorder) |
Inferred relationship |
Some |
|
Congenital ectodermal dysplasia of face |
Is a |
False |
Congenital anomaly of face (disorder) |
Inferred relationship |
Some |
|
Congenital malformation of tongue, mouth and pharynx |
Is a |
True |
Congenital anomaly of face (disorder) |
Inferred relationship |
Some |
|
Robinow-like syndrome |
Is a |
False |
Congenital anomaly of face (disorder) |
Inferred relationship |
Some |
|
Congenital melanocytic nevus of face |
Is a |
True |
Congenital anomaly of face (disorder) |
Inferred relationship |
Some |
|
A Noonan-related syndrome, characterized by facial anomalies suggestive of Noonan syndrome, loose anagen hair, frequent congenital heart defects, distinctive skin features (darkly pigmented skin, keratosis pilaris, eczema or icthyosis), and short stature that is often associated with a growth hormone deficiency. Psychomotor delay with attention deficit/hyperactivity disorder (ADHD) is frequently observed. |
Is a |
True |
Congenital anomaly of face (disorder) |
Inferred relationship |
Some |
|
Diprosopus |
Is a |
True |
Congenital anomaly of face (disorder) |
Inferred relationship |
Some |
|
Floating-Harbor syndrome |
Is a |
True |
Congenital anomaly of face (disorder) |
Inferred relationship |
Some |
|
Preauricular dimple |
Is a |
True |
Congenital anomaly of face (disorder) |
Inferred relationship |
Some |
|
Centrofacial lentiginosis syndrome |
Is a |
False |
Congenital anomaly of face (disorder) |
Inferred relationship |
Some |
|
Naso-labial cyst |
Is a |
True |
Congenital anomaly of face (disorder) |
Inferred relationship |
Some |
|
A rare developmental defect during embryogenesis characterized by macrostomia or abnormal mouth contour, preauricular tags or pits, and uni- or bilateral ptosis due to external ophthalmoplegia. This syndrome belongs to the oculoauriculovertebral spectrum, a developmental disorder affecting the structures derived from the first and second branchial arches. |
Is a |
False |
Congenital anomaly of face (disorder) |
Inferred relationship |
Some |
|
A rare genetic multiple congenital anomalies/dysmorphic syndrome characterized by psychomotor and growth delay, severe intellectual disability, microcephaly, and hypoplastic corpus callosum. Additional reported manifestations include increased muscle tonus, seizures, cardiac anomalies, recurrent bronchopneumonia, camptodactyly, preauricular skin tag, and dysmorphic facial features (such as broad forehead, hypertelorism, flat nasal bridge, anteverted nostrils, and prominent ears), among others. |
Is a |
False |
Congenital anomaly of face (disorder) |
Inferred relationship |
Some |
|
Weissenbacher-Zweymuller syndrome |
Is a |
False |
Congenital anomaly of face (disorder) |
Inferred relationship |
Some |
|
Robinow syndrome (RS) is a rare genetic syndrome characterized by limb shortening and abnormalities of the head, face and external genitalia. |
Is a |
False |
Congenital anomaly of face (disorder) |
Inferred relationship |
Some |
|
Congenital anomaly of lacrimal bone |
Is a |
False |
Congenital anomaly of face (disorder) |
Inferred relationship |
Some |
|
Global developmental delay-lung cysts-overgrowth-Wilms tumor syndrome is a rare, genetic, overgrowth syndrome characterized by global developmental delay, macrosomia with subsequent somatic overgrowth, bilateral cystic lung lesions, congenital nephromegaly and bilateral Wilms tumor. Craniofacial dysmorphism includes macrocephaly, frontal bossing, large anterior fontanelle, mild hypertelorism, ear pit, flat nasal bridge, anteverted nares and mild micrognathia. Additional features may include brain and skeletal anomalies, enlarged protuberant abdomen, fat pads on dorsum of feet and toes, and rugated soles with skin folds, as well as umbilical/inguinal hernia and autistic behavior. |
Is a |
True |
Congenital anomaly of face (disorder) |
Inferred relationship |
Some |
|
A disorder that is the mildest form of otopalatodigital syndrome spectrum disorder, and is characterised by a generalised skeletal dysplasia, mild intellectual disability, conductive hearing loss, and typical facial anomalies. |
Is a |
True |
Congenital anomaly of face (disorder) |
Inferred relationship |
Some |
|
A severe form of otopalatodigital syndrome spectrum disorder, and is characterized by dysmorphic facies, severe skeletal dysplasia affecting the axial and appendicular skeleton, extraskeletal anomalies (including malformations of the brain, heart, genitourinary system, and intestine) and poor survival. |
Is a |
True |
Congenital anomaly of face (disorder) |
Inferred relationship |
Some |
|
Preauricular cyst (disorder) |
Is a |
True |
Congenital anomaly of face (disorder) |
Inferred relationship |
Some |
|
Congenital temporomandibular joint ankylosis is a rare maxillofacial disorder characterized by significant reduction in mouth opening (i.e. from a few millimeters to a few centimeters) in the absence of acquired factors (e.g. trauma, infection) contributing to the ankylosis. It is associated with variable degrees of facial dysmorphism (i.e. lateral deviation of the mandible and chin, lower facial asymmetry, retrognathia, micrognathia, dental malocclusion) and patients typically present with feeding and breathing difficulties. Developmental delay, hypotonia, seizures, and additional dysmorphic features (e.g. pectus excavatum, low-set ears, hypoplastic alae nasi) have also been reported. |
Is a |
True |
Congenital anomaly of face (disorder) |
Inferred relationship |
Some |
|
Basal encephalocele (disorder) |
Is a |
False |
Congenital anomaly of face (disorder) |
Inferred relationship |
Some |
|
De Barsy syndrome (DBS) is characterized by facial dysmorphism (down-slanting palpebral fissures, a broad flat nasal bridge and a small mouth) with a progeroid appearance, large and late-closing fontanel, cutis laxa (CL), joint hyperlaxity, athetoid movements and hyperreflexia, pre- and postnatal growth retardation, intellectual deficit and developmental delay, and corneal clouding and cataract. |
Is a |
False |
Congenital anomaly of face (disorder) |
Inferred relationship |
Some |
|
A rare syndrome described and characterized by prenatal onset of growth deficiency, microcephaly, hypoplastic genitalia, and birth onset of convulsions. |
Is a |
True |
Congenital anomaly of face (disorder) |
Inferred relationship |
Some |
|
Congenital infiltrating lipomatosis of face (disorder) |
Is a |
True |
Congenital anomaly of face (disorder) |
Inferred relationship |
Some |
|
A rare, isolated, congenital, head and neck morphological anomaly characterised by the unilateral hypoplasia/agenesis of the depressor anguli oris muscle, resulting in an asymmetric crying facies in neonatal period/infancy (drooping of one corner of the mouth during crying) while eye closure, nasolabial fold and forehead wrinkling are symmetric. Although isolated in the majority of cases, newborns presenting with this morphological anomaly should be referred for further screening for 22q11.2 deletion syndrome and/or other coexisting cardiovascular, musculoskeletal, cervicofacial, respiratory, genitourinary and endocrine anomalies. |
Is a |
True |
Congenital anomaly of face (disorder) |
Inferred relationship |
Some |
|
Ectopic parotid gland tissue |
Is a |
True |
Congenital anomaly of face (disorder) |
Inferred relationship |
Some |
|
Accessory parotid gland |
Is a |
True |
Congenital anomaly of face (disorder) |
Inferred relationship |
Some |
|
Aplasia of parotid gland |
Is a |
True |
Congenital anomaly of face (disorder) |
Inferred relationship |
Some |
|
Oculopharyngeal muscular dystrophy (disorder) |
Is a |
True |
Congenital anomaly of face (disorder) |
Inferred relationship |
Some |
|
Congenital conjunctival cyst |
Is a |
True |
Congenital anomaly of face (disorder) |
Inferred relationship |
Some |
|
Strabismus fixus |
Is a |
True |
Congenital anomaly of face (disorder) |
Inferred relationship |
Some |
|
Supernumerary eye muscle |
Is a |
True |
Congenital anomaly of face (disorder) |
Inferred relationship |
Some |
|
Hypoplasia of eye muscle |
Is a |
True |
Congenital anomaly of face (disorder) |
Inferred relationship |
Some |
|
Congenital superior sulcus anomaly of orbit |
Is a |
True |
Congenital anomaly of face (disorder) |
Inferred relationship |
Some |
|
Congenital malformation of vitreous humour |
Is a |
True |
Congenital anomaly of face (disorder) |
Inferred relationship |
Some |
|
Congenital malformation of blood vessel of orbit proper (disorder) |
Is a |
True |
Congenital anomaly of face (disorder) |
Inferred relationship |
Some |
|
Congenital hypoplasia of middle third of face (disorder) |
Is a |
True |
Congenital anomaly of face (disorder) |
Inferred relationship |
Some |
|