Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Mixed germ cell neoplasm of central nervous system (disorder) |
Finding site |
True |
Structure of central nervous system |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Quantitative electroencephalogram (procedure) |
Procedure site - Direct (attribute) |
True |
Structure of central nervous system |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Intracranial hypotension due to cerebrospinal fluid fistula (disorder) |
Finding site |
True |
Structure of central nervous system |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Nongerminomatous germ cell tumor of central nervous system (disorder) |
Finding site |
True |
Structure of central nervous system |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Malformation of central nervous system of fetus (disorder) |
Finding site |
True |
Structure of central nervous system |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Spontaneous intracranial hypotension (disorder) |
Finding site |
True |
Structure of central nervous system |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
A very rare and severe type of NAGA deficiency characterised by infantile neuroaxonal dystrophy. |
Finding site |
False |
Structure of central nervous system |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Alpha-N-acetylgalactosaminidase deficiency type 2 |
Finding site |
False |
Structure of central nervous system |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Alpha-N-acetylgalactosaminidase deficiency type 3 (disorder) |
Finding site |
False |
Structure of central nervous system |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Implantable analgesic spinal cord electrical stimulation system pulse generator (physical object) |
Has device intended site (attribute) |
True |
Structure of central nervous system |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Cockayne syndrome type 3 |
Finding site |
True |
Structure of central nervous system |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Cockayne syndrome type 1 |
Finding site |
True |
Structure of central nervous system |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Cockayne syndrome type 2 (disorder) |
Finding site |
True |
Structure of central nervous system |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Bilateral upper motor neurone lesion |
Finding site |
True |
Structure of central nervous system |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Lesion of left upper motor neuron (finding) |
Finding site |
True |
Structure of central nervous system |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Lesion of right upper motor neuron |
Finding site |
True |
Structure of central nervous system |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Upper motor neurone lesion |
Finding site |
True |
Structure of central nervous system |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Hemiparesis of left side of face (disorder) |
Finding site |
True |
Structure of central nervous system |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Hemiparesis of right side of face (disorder) |
Finding site |
True |
Structure of central nervous system |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Fetal spina bifida (disorder) |
Finding site |
True |
Structure of central nervous system |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Neonatal agitation (disorder) |
Finding site |
True |
Structure of central nervous system |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Neonatal hypokinesia |
Finding site |
True |
Structure of central nervous system |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Coma in the newborn |
Finding site |
True |
Structure of central nervous system |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Pure autonomic failure |
Finding site |
True |
Structure of central nervous system |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
Deficiency of leukotriene C4 synthase |
Finding site |
True |
Structure of central nervous system |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
Parkinsonian syndrome with idiopathic orthostatic hypotension (disorder) |
Finding site |
True |
Structure of central nervous system |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
5 |
Pseudoprogeria syndrome |
Finding site |
True |
Structure of central nervous system |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
6 |
Progressive cerebellar ataxia with hypogonadism |
Finding site |
True |
Structure of central nervous system |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Primary primitive neuroectodermal neoplasm of central nervous system |
Finding site |
True |
Structure of central nervous system |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Spastic paralysis due to birth injury |
Finding site |
True |
Structure of central nervous system |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Autosomal dominant polycystic kidney disease type 1 with tuberous sclerosis (disorder) |
Finding site |
True |
Structure of central nervous system |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Fibrous skin tumor of tuberous sclerosis |
Finding site |
True |
Structure of central nervous system |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
5 |
Tuberous sclerosis syndrome |
Finding site |
True |
Structure of central nervous system |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Pulmonary tuberous sclerosis (disorder) |
Finding site |
True |
Structure of central nervous system |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
7 |
Anaplastic oligodendroglioma of central nervous system (disorder) |
Finding site |
True |
Structure of central nervous system |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Anaplastic ependymoma of central nervous system |
Finding site |
True |
Structure of central nervous system |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Anaplastic oligoastrocytoma of central nervous system (disorder) |
Finding site |
True |
Structure of central nervous system |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Angiocentric glioma of central nervous system |
Finding site |
True |
Structure of central nervous system |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Anaplastic ganglioglioma of central nervous system (disorder) |
Finding site |
True |
Structure of central nervous system |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Cerebrospinal fluid shunt port/reservoir (physical object) |
Has device intended site (attribute) |
True |
Structure of central nervous system |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Germinoma of central nervous system (disorder) |
Finding site |
True |
Structure of central nervous system |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Cerebrospinal fluid shunt catheter plug |
Has device intended site (attribute) |
True |
Structure of central nervous system |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Lumbar or thoracic cerebrospinal fluid shunt subcutaneous anchor |
Has device intended site (attribute) |
True |
Structure of central nervous system |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Gliosarcoma of central nervous system |
Finding site |
True |
Structure of central nervous system |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Giant cell glioblastoma of central nervous system |
Finding site |
True |
Structure of central nervous system |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Gemistocytic astrocytoma of central nervous system |
Finding site |
True |
Structure of central nervous system |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Fibrillary astrocytoma of central nervous system |
Finding site |
True |
Structure of central nervous system |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Astroblastoma of central nervous system |
Finding site |
True |
Structure of central nervous system |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
2-methyl-3-hydroxybutyric aciduria |
Finding site |
True |
Structure of central nervous system |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Central nervous system deficit (finding) |
Finding site |
True |
Structure of central nervous system |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Parasitic infection of central nervous system |
Finding site |
False |
Structure of central nervous system |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
TBCK-related intellectual disability syndrome |
Finding site |
True |
Structure of central nervous system |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
RERE-related neurodevelopmental syndrome |
Finding site |
True |
Structure of central nervous system |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Telomere maintenance 2-related intellectual disability, neurodevelopmental disorder (disorder) |
Finding site |
True |
Structure of central nervous system |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Non-Hodgkin lymphoma of central nervous system metastatic to lymph node of lower limb |
Finding site |
True |
Structure of central nervous system |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Non-Hodgkin lymphoma of central nervous system metastatic to lymph node of upper limb (disorder) |
Finding site |
True |
Structure of central nervous system |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Intraocular non-Hodgkin malignant lymphoma (disorder) |
Finding site |
True |
Structure of central nervous system |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Granuloma of central nervous system caused by Schistosoma (disorder) |
Finding site |
True |
Structure of central nervous system |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Paediatric multiple sclerosis |
Finding site |
True |
Structure of central nervous system |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Paediatric multiple sclerosis |
Finding site |
True |
Structure of central nervous system |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Psychomotor regression, oculomotor apraxia, movement disorder, nephropathy syndrome (disorder) |
Finding site |
True |
Structure of central nervous system |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Mitochondrial respiratory chain complex I structural subunit gene defect |
Finding site |
True |
Structure of central nervous system |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Mitochondrial respiratory chain complex I assembly gene defect |
Finding site |
True |
Structure of central nervous system |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Yolk sac tumour of central nervous system |
Finding site |
True |
Structure of central nervous system |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Primary choriocarcinoma of central nervous system |
Finding site |
True |
Structure of central nervous system |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Primary choriocarcinoma of central nervous system |
Finding site |
False |
Structure of central nervous system |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
A rare autosomal ichthyosis syndrome with prominent neurologic signs characterized by the association of congenital ichthyosis with global developmental delay, intellectual disability, infantile-onset seizures, and spastic tetraplegia. Brain imaging may show delayed myelination and cerebral atrophy. Marked intrafamilial variability has been reported. |
Finding site |
True |
Structure of central nervous system |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
5 |
A rare multiple congenital anomalies/dysmorphic syndrome characterized by global developmental delay or regression, variable congenital heart defects (such as patent ductus arteriosus, atrial or ventricular septal defects, and double outlet right ventricle, among others), and dysmorphic features (including ptosis, epicanthal folds, abnormally set/dysplastic ears, low hairline or excess nuchal skin, wide-spaced/inverted nipples, umbilical hernia or diastasis recti, and digital anomalies). Additional variable manifestations are hyper- or hypotonia, seizures, hearing loss, cortical blindness, and optic atrophy. Brain imaging may show cerebral and cerebellar atrophy and hydrocephalus. |
Finding site |
True |
Structure of central nervous system |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Intracranial hypotension following ventricular shunting (disorder) |
Finding site |
True |
Structure of central nervous system |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
Prune exopolyphosphatase 1-related neurological syndrome (disorder) |
Finding site |
True |
Structure of central nervous system |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Global developmental delay, alopecia, macrocephaly, facial dysmorphism, structural brain anomalies syndrome |
Finding site |
True |
Structure of central nervous system |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
Myelin oligodendrocyte glycoprotein antibody-associated disease (disorder) |
Finding site |
True |
Structure of central nervous system |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Myelin oligodendrocyte glycoprotein antibody-associated disease (disorder) |
Finding site |
True |
Structure of central nervous system |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Primary oculocerebral non-Hodgkin lymphoma (disorder) |
Finding site |
True |
Structure of central nervous system |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Metastatic neuroblastoma to central nervous system (disorder) |
Finding site |
True |
Structure of central nervous system |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Juvenile-onset diabetes mellitus, central and peripheral neurodegeneration syndrome |
Finding site |
True |
Structure of central nervous system |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Obstetric anesthesia with central nervous system complications - delivered |
Finding site |
False |
Structure of central nervous system |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Obstetric anesthesia with central nervous system complication - delivered with postnatal problem |
Finding site |
False |
Structure of central nervous system |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Obstetric anesthesia with central nervous system complication with antenatal problem |
Finding site |
False |
Structure of central nervous system |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
anesthésie obstétricale avec complication du système nerveux central et problème postnatal |
Finding site |
False |
Structure of central nervous system |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Obstetric anesthesia with central nervous system complication in childbirth |
Finding site |
True |
Structure of central nervous system |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Amyotrophic lateral sclerosis with multiple system atrophy |
Finding site |
True |
Structure of central nervous system |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Central nervous system demyelination due to Whipple disease |
Finding site |
True |
Structure of central nervous system |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Central nervous system demyelination due to Lyme borreliosis |
Finding site |
True |
Structure of central nervous system |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Autonomic disorder due to multiple sclerosis |
Finding site |
True |
Structure of central nervous system |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Autonomic disorder due to multiple sclerosis |
Finding site |
True |
Structure of central nervous system |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
Primary neuroblastoma of central nervous system |
Finding site |
True |
Structure of central nervous system |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Primary ganglioneuroblastoma of central nervous system (disorder) |
Finding site |
True |
Structure of central nervous system |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Primary glioblastoma multiforme of central nervous system |
Finding site |
True |
Structure of central nervous system |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Primary malignant glioma of central nervous system (disorder) |
Finding site |
True |
Structure of central nervous system |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Primary anaplastic oligoastrocytoma of central nervous system (disorder) |
Finding site |
True |
Structure of central nervous system |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Primary anaplastic ganglioglioma of central nervous system (disorder) |
Finding site |
True |
Structure of central nervous system |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Primary mixed germ cell neoplasm of central nervous system |
Finding site |
True |
Structure of central nervous system |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Chronic inflammatory demyelinating disease of peripheral nervous system and central nervous system (disorder) |
Finding site |
True |
Structure of central nervous system |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Chronic inflammatory demyelinating disease of peripheral nervous system and central nervous system (disorder) |
Finding site |
True |
Structure of central nervous system |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Presence of regression of primary malignant neoplasm of central nervous system after neoadjuvant antineoplastic therapy (observable entity) |
Inherent location (attribute) |
False |
Structure of central nervous system |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
8 |
Increased cerebrospinal fluid production due to choroid plexus carcinoma (disorder) |
Finding site |
True |
Structure of central nervous system |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Increased cerebrospinal fluid production due to benign papilloma of choroid plexus (disorder) |
Finding site |
True |
Structure of central nervous system |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Increased cerebrospinal fluid production due to hyperplasia of choroid plexus (disorder) |
Finding site |
True |
Structure of central nervous system |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Intracranial hypotension due to cerebrospinal fluid otorrhea (disorder) |
Finding site |
True |
Structure of central nervous system |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Intracranial hypotension due to cerebrospinal fluid rhinorrhoea |
Finding site |
True |
Structure of central nervous system |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |