Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Panhypopituitarism - anterior and posterior |
Is a |
True |
Disorder of posterior pituitary |
Inferred relationship |
Some |
|
Oxytocin deficiency |
Is a |
True |
Disorder of posterior pituitary |
Inferred relationship |
Some |
|
Syndrome of diencephalo-hypophyseal origin |
Is a |
True |
Disorder of posterior pituitary |
Inferred relationship |
Some |
|
Congenital malformation of posterior pituitary |
Is a |
True |
Disorder of posterior pituitary |
Inferred relationship |
Some |
|
diabetes insipidus |
Is a |
False |
Disorder of posterior pituitary |
Inferred relationship |
Some |
|
Syndrome of inappropriate vasopressin secretion |
Is a |
True |
Disorder of posterior pituitary |
Inferred relationship |
Some |
|
andre sygdomme i neurohypofysen |
Is a |
False |
Disorder of posterior pituitary |
Inferred relationship |
Some |
|
Granular cell tumour of neurohypophysis |
Is a |
True |
Disorder of posterior pituitary |
Inferred relationship |
Some |
|
Spindle cell oncocytoma of posterior pituitary gland (disorder) |
Is a |
True |
Disorder of posterior pituitary |
Inferred relationship |
Some |
|
Pituicytoma of posterior pituitary gland (disorder) |
Is a |
True |
Disorder of posterior pituitary |
Inferred relationship |
Some |
|
Sellar ependymoma of posterior pituitary gland |
Is a |
True |
Disorder of posterior pituitary |
Inferred relationship |
Some |
|
Vasopressin deficiency |
Is a |
True |
Disorder of posterior pituitary |
Inferred relationship |
Some |
|
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. |
Is a |
False |
Disorder of posterior pituitary |
Inferred relationship |
Some |
|