Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Entire body of corpus callosum |
partie de |
False |
Entire corpus callosum |
Additional relationship (core metadata concept) |
Existential restriction modifier (core metadata concept) |
|
Entire genu of corpus callosum |
partie de |
False |
Entire corpus callosum |
Additional relationship (core metadata concept) |
Existential restriction modifier (core metadata concept) |
|
Entire rostrum of corpus callosum |
partie de |
False |
Entire corpus callosum |
Additional relationship (core metadata concept) |
Existential restriction modifier (core metadata concept) |
|
Entire splenium of corpus callosum |
partie de |
False |
Entire corpus callosum |
Additional relationship (core metadata concept) |
Existential restriction modifier (core metadata concept) |
|
Structure of splenium of corpus callosum |
partie de |
False |
Entire corpus callosum |
Additional relationship (core metadata concept) |
Existential restriction modifier (core metadata concept) |
|
Structure of temporal radiation of corpus callosum |
partie de |
False |
Entire corpus callosum |
Additional relationship (core metadata concept) |
Existential restriction modifier (core metadata concept) |
|
Structure of lamina terminalis of corpus callosum |
partie de |
False |
Entire corpus callosum |
Additional relationship (core metadata concept) |
Existential restriction modifier (core metadata concept) |
|
Structure of forceps minor (body structure) |
partie de |
False |
Entire corpus callosum |
Additional relationship (core metadata concept) |
Existential restriction modifier (core metadata concept) |
|
Structure of rostrum of corpus callosum |
partie de |
False |
Entire corpus callosum |
Additional relationship (core metadata concept) |
Existential restriction modifier (core metadata concept) |
|
Structure of genu of corpus callosum |
partie de |
False |
Entire corpus callosum |
Additional relationship (core metadata concept) |
Existential restriction modifier (core metadata concept) |
|
Structure of body of corpus callosum |
partie de |
False |
Entire corpus callosum |
Additional relationship (core metadata concept) |
Existential restriction modifier (core metadata concept) |
|
Entire forceps minor |
partie de |
False |
Entire corpus callosum |
Additional relationship (core metadata concept) |
Existential restriction modifier (core metadata concept) |
|
Entire temporal radiation of corpus callosum (body structure) |
partie de |
False |
Entire corpus callosum |
Additional relationship (core metadata concept) |
Existential restriction modifier (core metadata concept) |
|
Entire lamina terminalis of corpus callosum |
partie de |
False |
Entire corpus callosum |
Additional relationship (core metadata concept) |
Existential restriction modifier (core metadata concept) |
|
Agenesis of corpus callosum |
Finding site |
True |
Entire corpus callosum |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Aicardi's syndrome |
Finding site |
False |
Entire corpus callosum |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Agenesis of corpus callosum with lipoma |
Finding site |
True |
Entire corpus callosum |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
A rare polymalformative syndrome characterized by agenesis of corpus callosum (CC), distal anomalies of limbs, minor craniofacial anomalies and intellectual disability. |
Finding site |
False |
Entire corpus callosum |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
X-linked lissencephaly with agenesis of corpus callosum and genital anomaly syndrome (disorder) |
Finding site |
False |
Entire corpus callosum |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
syndrome de déficience intellectuelle liée à l'X-agénésie du corps calleux-quadriparésie spastique |
Finding site |
False |
Entire corpus callosum |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Vici syndrome (disorder) |
Finding site |
False |
Entire corpus callosum |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
5 |
A very rare congenital genetic neurological disorder characterised by agenesis/hypoplasia of corpus callosum with developmental abnormalities, ocular disorders, and variable craniofacial and skeletal abnormalities. |
Finding site |
False |
Entire corpus callosum |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
Curry-Jones syndrome is a form of syndromic craniosynostosis characterised by unilateral coronal craniosynostosis or multiple suture synostosis associated with complete or partial agenesis of the corpus callosum, preaxial polysyndactyly and syndactyly of hands and/or feet, along with anomalies of the skin (characteristic pearly white areas that become scarred and atrophic, abnormal hair growth around the eyes and/or cheeks, and on the limbs), eyes (iris colobomas, microphthalmia,) and intestine (congenital short gut, malrotation, dysmotility, chronic constipation, bleeding and myofibromas). Developmental delay and variable degrees of intellectual disability may also be observed. Multiple intra-abdominal smooth muscle hamartomas, trichoblastoma of the skin, occipital meningoceles and development of desmoplastic medulloblastoma have been reported. |
Finding site |
False |
Entire corpus callosum |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
5 |
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. |
Finding site |
False |
Entire corpus callosum |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
Infantile osteopetrosis with neuroaxonal dysplasia syndrome (disorder) |
Finding site |
False |
Entire corpus callosum |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Infantile osteopetrosis with neuroaxonal dysplasia syndrome (disorder) |
Finding site |
True |
Entire corpus callosum |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Agenesis of corpus callosum and abnormal genitalia syndrome |
Finding site |
True |
Entire corpus callosum |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Agenesis of corpus callosum and abnormal genitalia syndrome |
Finding site |
False |
Entire corpus callosum |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Vici syndrome (disorder) |
Finding site |
True |
Entire corpus callosum |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
syndrome de déficience intellectuelle liée à l'X-agénésie du corps calleux-quadriparésie spastique |
Finding site |
False |
Entire corpus callosum |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
X-linked lissencephaly with agenesis of corpus callosum and genital anomaly syndrome (disorder) |
Finding site |
True |
Entire corpus callosum |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
A rare polymalformative syndrome characterized by agenesis of corpus callosum (CC), distal anomalies of limbs, minor craniofacial anomalies and intellectual disability. |
Finding site |
True |
Entire corpus callosum |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
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. |
Finding site |
True |
Entire corpus callosum |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Microcephaly, polymicrogyria, corpus callosum agenesis syndrome (disorder) |
Finding site |
True |
Entire corpus callosum |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
X-linked cerebral, cerebellar, coloboma syndrome (disorder) |
Finding site |
True |
Entire corpus callosum |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Agenesis of corpus callosum, macrocephaly, hypertelorism syndrome |
Finding site |
True |
Entire corpus callosum |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
5 |
Severe intellectual disability, agenesis of corpus callosum, facial dysmorphism, cerebellar ataxia syndrome (disorder) |
Finding site |
True |
Entire corpus callosum |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |