Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Entire neurohypophysis |
Is a |
True |
Neurohypophysis structure |
Inferred relationship |
Some |
|
Pars nervosa of pituitary gland |
Is a |
False |
Neurohypophysis structure |
Inferred relationship |
Some |
|
Entire infundibulum of pituitary gland |
Is a |
False |
Neurohypophysis structure |
Inferred relationship |
Some |
|
Median eminence of hypothalamus |
Is a |
False |
Neurohypophysis structure |
Inferred relationship |
Some |
|
Structure of infundibular diverticulum |
Is a |
True |
Neurohypophysis structure |
Inferred relationship |
Some |
|
Excision of lesion of pituitary gland |
Procedure site |
False |
Neurohypophysis structure |
Inferred relationship |
Some |
1 |
Biopsy of lesion of pituitary gland |
Procedure site |
False |
Neurohypophysis structure |
Inferred relationship |
Some |
|
Operation on lesion of pituitary gland |
Procedure site |
False |
Neurohypophysis structure |
Inferred relationship |
Some |
|
Panhypopituitarism - anterior and posterior |
Finding site |
True |
Neurohypophysis structure |
Inferred relationship |
Some |
1 |
Syndrome of diencephalo-hypophyseal origin |
Finding site |
True |
Neurohypophysis structure |
Inferred relationship |
Some |
1 |
Secondary arginine vasopressin-related polyuria (disorder) |
Finding site |
False |
Neurohypophysis structure |
Inferred relationship |
Some |
1 |
diabète insipide |
Finding site |
False |
Neurohypophysis structure |
Inferred relationship |
Some |
1 |
Pituicyte |
partie de |
False |
Neurohypophysis structure |
Additional relationship |
Some |
|
Familial vasopressin-related polyuria |
Finding site |
False |
Neurohypophysis structure |
Inferred relationship |
Some |
1 |
Herring body |
partie de |
False |
Neurohypophysis structure |
Additional relationship |
Some |
|
Vasopressin deficiency |
Finding site |
True |
Neurohypophysis structure |
Inferred relationship |
Some |
1 |
diabète insipide néphrogénique héréditaire |
Finding site |
False |
Neurohypophysis structure |
Inferred relationship |
Some |
|
Vasopressin deficiency syndrome |
Finding site |
False |
Neurohypophysis structure |
Inferred relationship |
Some |
|
A rare, genetic, endocrine disorder characterised by type I diabetes mellitus (DM), diabetes insipidus (DI), sensorineural deafness (D), bilateral optical atrophy (OA) and neurological signs. |
Finding site |
False |
Neurohypophysis structure |
Inferred relationship |
Some |
2 |
Disorder of posterior pituitary |
Finding site |
True |
Neurohypophysis structure |
Inferred relationship |
Some |
1 |
Idiopathic arginine vasopressin-related polyuria (disorder) |
Finding site |
False |
Neurohypophysis structure |
Inferred relationship |
Some |
1 |
Primary polydipsia |
Finding site |
False |
Neurohypophysis structure |
Inferred relationship |
Some |
1 |
Other disorders of neurohypophysis |
Finding site |
False |
Neurohypophysis structure |
Inferred relationship |
Some |
|
Other disorder of neurohypophysis NOS |
Finding site |
False |
Neurohypophysis structure |
Inferred relationship |
Some |
|
Hypohidrosis-diabetes insipidus syndrome |
Finding site |
False |
Neurohypophysis structure |
Inferred relationship |
Some |
4 |
Arginine vasopressin resistance (disorder) |
Finding site |
False |
Neurohypophysis structure |
Inferred relationship |
Some |
1 |
diabète insipide néphrogénique médicamenteux |
Finding site |
False |
Neurohypophysis structure |
Inferred relationship |
Some |
2 |
Acquired vasopressin resistance |
Finding site |
False |
Neurohypophysis structure |
Inferred relationship |
Some |
2 |
Structure of infundibulum of pituitary gland |
Is a |
False |
Neurohypophysis structure |
Inferred relationship |
Some |
|
Structure of neural lobe of neurohypophysis (body structure) |
Is a |
True |
Neurohypophysis structure |
Inferred relationship |
Some |
|
Familial vasopressin deficiency |
Finding site |
True |
Neurohypophysis structure |
Inferred relationship |
Some |
1 |
Oxytocin deficiency |
Finding site |
True |
Neurohypophysis structure |
Inferred relationship |
Some |
1 |
Congenital malformation of posterior pituitary |
Finding site |
False |
Neurohypophysis structure |
Inferred relationship |
Some |
1 |
Syndrome of inappropriate vasopressin secretion |
Finding site |
True |
Neurohypophysis structure |
Inferred relationship |
Some |
1 |
Schwartz syndrome |
Finding site |
False |
Neurohypophysis structure |
Inferred relationship |
Some |
|
Congenital malformation of posterior pituitary |
Finding site |
True |
Neurohypophysis structure |
Inferred relationship |
Some |
1 |
Structure of infundibular stem of neurohypophysis (body structure) |
Is a |
True |
Neurohypophysis structure |
Inferred relationship |
Some |
|
Granular cell tumour of neurohypophysis |
Finding site |
True |
Neurohypophysis structure |
Inferred relationship |
Some |
1 |
Congenital malformation of posterior pituitary |
Finding site |
False |
Neurohypophysis structure |
Inferred relationship |
Some |
2 |
Partial vasopressin resistance |
Finding site |
False |
Neurohypophysis structure |
Inferred relationship |
Some |
1 |
Partial vasopressin-related polyuria |
Finding site |
False |
Neurohypophysis structure |
Inferred relationship |
Some |
1 |
A rare, genetic, renal tubular disease characterized by nephrogenic diabetes insipidus, intracerebral calcifications, intellectual disability, short stature and facial dysmorphism. There have been no further descriptions in the literature since 1990. |
Finding site |
False |
Neurohypophysis structure |
Inferred relationship |
Some |
2 |
X-linked intellectual disability-limb spasticity-retinal dystrophy-diabetes insipidus syndrome is a rare genetic neurometabolic disease characterized by severe intellectual disability, spastic quadriparesis, Leber congenital amaurosis and diabetes insipidus. Additional manifestations include facial dysmorphy (dolichocephalic skull, hypertelorism, deep-set eyes, hypoplastic nares, low-set ears), short stature, truncal hypotonia and axial hypertonia. Brain anomalies (e.g. thin corpus callosum with lack of isthmus and tapered splenium, hypoplasia or atrophy of the optic chiasm, prominent lateral ventricles, diminished white matter), described on magnetic resonance imaging, have been reported. High prenatal alpha-fetoprotein and intrauterine growth restriction is observed in routine pregnancy examination. |
Finding site |
True |
Neurohypophysis structure |
Inferred relationship |
Some |
3 |
diabète insipide néphrogénique héréditaire |
Finding site |
False |
Neurohypophysis structure |
Inferred relationship |
Some |
1 |
Spindle cell oncocytoma of posterior pituitary gland (disorder) |
Finding site |
True |
Neurohypophysis structure |
Inferred relationship |
Some |
1 |
Pituicytoma of posterior pituitary gland (disorder) |
Finding site |
True |
Neurohypophysis structure |
Inferred relationship |
Some |
1 |
Sellar ependymoma of posterior pituitary gland |
Finding site |
True |
Neurohypophysis structure |
Inferred relationship |
Some |
1 |
Postoperative vasopressin deficiency |
Finding site |
True |
Neurohypophysis structure |
Inferred relationship |
Some |
2 |
Ectopic syndrome of inappropriate secretion of antidiuretic hormone |
Finding site |
True |
Neurohypophysis structure |
Inferred relationship |
Some |
1 |
Arginine vasopressin deficiency due to trauma (disorder) |
Finding site |
True |
Neurohypophysis structure |
Inferred relationship |
Some |
2 |
Pituitary syndrome of inappropriate vasopressin secretion |
Finding site |
True |
Neurohypophysis structure |
Inferred relationship |
Some |
1 |
Autosomal dominant hereditary arginine vasopressin deficiency (disorder) |
Finding site |
True |
Neurohypophysis structure |
Inferred relationship |
Some |
2 |
Autosomal recessive hereditary arginine vasopressin deficiency (disorder) |
Finding site |
True |
Neurohypophysis structure |
Inferred relationship |
Some |
2 |
Secondary vasopressin deficiency |
Finding site |
True |
Neurohypophysis structure |
Inferred relationship |
Some |
2 |
Congenital hypoplasia of posterior pituitary |
Finding site |
True |
Neurohypophysis structure |
Inferred relationship |
Some |
1 |
Delayed onset arginine vasopressin deficiency due to and following traumatic brain injury (disorder) |
Finding site |
True |
Neurohypophysis structure |
Inferred relationship |
Some |
3 |