Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Axon hillock (cell structure) |
Is a |
True |
Axon structure (cell structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Entire axon |
Is a |
True |
Axon structure (cell structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Peripheral nerve axis cylinder |
Is a |
True |
Axon structure (cell structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Central nervous system axis cylinder |
Is a |
True |
Axon structure (cell structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Giant axonal neuropathy (disorder) |
Finding site |
False |
Axon structure (cell structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Dying back phenomenon |
Finding site |
False |
Axon structure (cell structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Dying back phenomenon |
Finding site |
False |
Axon structure (cell structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Ranvier's node |
Is a |
True |
Axon structure (cell structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Axonal neuropathy |
Finding site |
True |
Axon structure (cell structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Giant axonal neuropathy (disorder) |
Finding site |
True |
Axon structure (cell structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Axonal sensorimotor neuropathy |
Finding site |
True |
Axon structure (cell structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Moebius syndrome, axonal neuropathy, hypogonadotropic hypogonadism syndrome (disorder) |
Finding site |
True |
Axon structure (cell structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Peripheral axonal neuropathy (disorder) |
Finding site |
True |
Axon structure (cell structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Autosomal recessive axonal neuropathy with neuromyotonia |
Finding site |
True |
Axon structure (cell structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Ocular anomalies, axonal neuropathy, developmental delay syndrome (disorder) |
Finding site |
True |
Axon structure (cell structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Autosomal recessive lethal neonatal axonal sensorimotor polyneuropathy (disorder) |
Finding site |
True |
Axon structure (cell structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
5 |
Congenital axonal neuropathy with encephalopathy |
Finding site |
True |
Axon structure (cell structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
A rare neurologic disease characterized by axonal sensorimotor neuropathy, progressive optic atrophy, cognitive deficit, bulbar dysfunction, seizures, and early hypotonia and feeding difficulties. Additional possible features include dystonia, scoliosis, joint contractures, ocular anomalies, and urogenital anomalies. Brain MRI reveals variable degrees of cerebral atrophy. The disease is fatal in childhood due to respiratory failure. |
Finding site |
True |
Axon structure (cell structure) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
6 |