Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Dysgenesis of corpus callosum |
Is a |
False |
Congenital malformation of corpus callosum |
Inferred relationship |
Some |
|
Atrophy of corpus callosum |
Is a |
False |
Congenital malformation of corpus callosum |
Inferred relationship |
Some |
|
Agenesis of corpus callosum |
Is a |
False |
Congenital malformation of corpus callosum |
Inferred relationship |
Some |
|
Aplasia of corpus callosum |
Is a |
True |
Congenital malformation of corpus callosum |
Inferred relationship |
Some |
|
Anomaly of corpus callosum NOS |
Is a |
False |
Congenital malformation of corpus callosum |
Inferred relationship |
Some |
|
Agenesis of corpus callosum |
Is a |
False |
Congenital malformation of corpus callosum |
Inferred relationship |
Some |
|
Partial agenesis of corpus callosum |
Is a |
False |
Congenital malformation of corpus callosum |
Inferred relationship |
Some |
|
Hypoplasia of corpus callosum |
Is a |
True |
Congenital malformation of corpus callosum |
Inferred relationship |
Some |
|
A rare, genetic, syndromic intellectual disability disease characterized by progressive postnatal microcephaly and global developmental delay, as well as moderate to profound intellectual disability, difficulty or inability to walk, pyramidal signs (including spasticity, hyperreflexia and extensor plantar response) and thin corpus callosum revealed by brain imaging. Ophthalmologic signs (including nystagmus, strabismus and abnormal retinal pigmentation), foot deformity and genital anomalies may also be associated. |
Is a |
True |
Congenital malformation of corpus callosum |
Inferred relationship |
Some |
|
A rare frontonasal dysplasia characterized by median cleft of the upper lip (MCL), midline polyps of the facial skin, nasal mucosa, and pericallosal lipomas. Hypertelorism with ocular anomalies are also observed, generally with normal neuropsychological development. |
Is a |
False |
Congenital malformation of corpus callosum |
Inferred relationship |
Some |
|
Micro syndrome is an autosomal recessive disorder characterized by ocular and neurodevelopmental defects and by micro genitalia. It presents with severe intellectual disability, microcephaly, congenital cataract, microcornea, microphthalmia, agenesis/hypoplasia of the corpus callosum, and hypogenitalism. |
Is a |
True |
Congenital malformation of corpus callosum |
Inferred relationship |
Some |
|
A rare, genetic, multiple congenital anomalies/dysmorphic syndrome characterized by severe white matter hypoplasia, corpus callosum agenesis or extreme hypoplasia, severe intellectual disability, failure to thrive and minor midline facial dysmorphism (including hypertelorism, broad nasal root, micrognathia). There have been no further descriptions in the literature since 1993. |
Is a |
True |
Congenital malformation of corpus callosum |
Inferred relationship |
Some |
|
A rare neurometabolic disorder due to serine deficiency characterized by neonatal to infantile onset of global developmental delay, postnatal microcephaly and intellectual disability, which may be associated with slowly progressive spastic tetraplegia mainly affecting the lower extremities, seizures, and brain MRI findings including thin corpus callosum, delayed myelination and cerebral atrophy. Additional symptoms include brisk deep tendon reflexes, extensor plantar responses, behavioral abnormalities (such as irritability, hyperactivity, sleep disorder), abnormal hand movements and stereotypy. |
Is a |
True |
Congenital malformation of corpus callosum |
Inferred relationship |
Some |
|
A rare genetic multiple congenital anomalies/dysmorphic syndrome characterized by variable degrees of developmental delay and intellectual disability with poor or absent speech, hypotonia, hypoplastic or absent corpus callosum, and facial dysmorphism (such as long face, frontal bossing, hypertelorism, downslanting palpebral fissures, and tented upper lip). Additional reported features include microcephaly, seizures, gait ataxia, scoliosis, and syndactyly of fingers, among others. |
Is a |
True |
Congenital malformation of corpus callosum |
Inferred relationship |
Some |
|