Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Congenital maxillary hypoplasia |
Is a |
False |
Congenital micrognathism |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Brachygnathism |
Is a |
False |
Congenital micrognathism |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Congenital mandibular hypoplasia |
Is a |
False |
Congenital micrognathism |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Micrognathism unspecified |
Is a |
False |
Congenital micrognathism |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Cerebro-costo-mandibular syndrome |
Is a |
True |
Congenital micrognathism |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Congenital transverse mandibular hypoplasia |
Is a |
True |
Congenital micrognathism |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Congenital vertical mandibular hypoplasia |
Is a |
True |
Congenital micrognathism |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Congenital horizontal mandibular hypoplasia (disorder) |
Is a |
True |
Congenital micrognathism |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Corpus callosum agenesis-intellectual disability-coloboma-micrognathia syndrome is a developmental anomalies syndrome characterised by coloboma of the iris and optic nerve, facial dysmorphism (high forehead, microretrognathia, low-set ears), intellectual deficit, agenesis of the corpus callosum (ACC), sensorineural hearing loss, skeletal anomalies and short stature. |
Is a |
True |
Congenital micrognathism |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Agnathia, holoprosencephaly, situs inversus syndrome (disorder) |
Is a |
True |
Congenital micrognathism |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Distal limb deficiency with micrognathia syndrome |
Is a |
True |
Congenital micrognathism |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Thickened earlobe with conductive deafness syndrome (disorder) |
Is a |
True |
Congenital micrognathism |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Splenogonadal fusion, limb defect, micrognathia syndrome (disorder) |
Is a |
True |
Congenital micrognathism |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Mandibular hypoplasia, deafness, progeroid syndrome |
Is a |
True |
Congenital micrognathism |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Joint contracture, webbed neck, micrognathia, hypoplastic nipple syndrome (disorder) |
Is a |
True |
Congenital micrognathism |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Short stature, auditory canal atresia, mandibular hypoplasia, skeletal anomalies syndrome |
Is a |
True |
Congenital micrognathism |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
SATB2-associated syndrome |
Is a |
True |
Congenital micrognathism |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|