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37512009: Neurohypophysis structure (body structure)

SNOMED CT Concept\Body structure\Anatomical or acquired body structure (body structure)\Anatomical structure\...

\Anatomical structure which has as its parts a heterogeneous collection of organs, organ parts, cells, cell parts or body part subdivisions that are adjacent to, or continuous with one another; does not constitute a cell part, cell, tissue, organ, or body part subdivision.\Structure of anatomical compartment (body structure)\Intracranial structure\Brain structure\Brain part\Brain region\Supratentorial brain\Supratentorial brain part\The cerebrum is the regional structure of the brain, which is the adult equivalent of the forebrain or prosencephalon. It is constituted by the structural derivatives of the telencephalon and diencephalon including the cerebral hemispheres, epithalamus, thalamus, hypothalamus, lateral ventricles and third ventricle. This definition is harmonious with the Federation of Association of Anatomist Second Edition (2019) Part V Terminologia Anatomica.\Structure of diencephalon\Diencephalon part\Pituitary and/or pineal structures (body structure)\Pituitary structure\Pituitary part\Neurohypophysis structure

\Gland structure (body structure)\Endocrine gland structure (body structure)\...

\Pituitary and/or pineal structures (body structure)\Pituitary structure\Pituitary part\Neurohypophysis structure

\Endocrine gland part\Pituitary part\Neurohypophysis structure

\Body region structure\Body part structure\Upper body structure\Upper body part structure\Structure of head and/or neck (body structure)\Head structure\Head part\Intracranial structure\Brain structure\Brain part\Brain region\Supratentorial brain\Supratentorial brain part\The cerebrum is the regional structure of the brain, which is the adult equivalent of the forebrain or prosencephalon. It is constituted by the structural derivatives of the telencephalon and diencephalon including the cerebral hemispheres, epithalamus, thalamus, hypothalamus, lateral ventricles and third ventricle. This definition is harmonious with the Federation of Association of Anatomist Second Edition (2019) Part V Terminologia Anatomica.\Structure of diencephalon\Diencephalon part\Pituitary and/or pineal structures (body structure)\Pituitary structure\Pituitary part\Neurohypophysis structure

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Neurohypophysis structure	Is a	Pituitary part	true	Inferred relationship	Some
Neurohypophysis structure	del af	Entire pituitary gland	false	Additional relationship	Some

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
hypofysens infundibulum som helhed	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)	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
diabetes insipidus	Finding site	False	Neurohypophysis structure	Inferred relationship	Some	1
Pituicyte	del af	False	Neurohypophysis structure	Additional relationship	Some
Familial vasopressin-related polyuria	Finding site	False	Neurohypophysis structure	Inferred relationship	Some	1
Herring body	del af	False	Neurohypophysis structure	Additional relationship	Some
Vasopressin deficiency	Finding site	True	Neurohypophysis structure	Inferred relationship	Some	1
hereditær nefrogen diabetes insipidus	Finding site	False	Neurohypophysis structure	Inferred relationship	Some
Vasopressin deficiency syndrome	Finding site	False	Neurohypophysis structure	Inferred relationship	Some
A rare genetic endocrine disorder with characteristics of type 1 diabetes mellitus (DM), diabetes insipidus (DI), sensorineural deafness (D), bilateral optical atrophy (OA) and neurological signs. Two types of Wolfram syndrome may be distinguished: type 1 (WS1) and type 2 (WS2). Two causative genes have been identified: WFS1 (4p16.1) and CISD2 (4q24). The clinical criteria for Wolfram syndrome diagnosis are juvenile-onset diabetes mellitus and optic atrophy, family history of Wolfram syndrome or diabetes mellitus and deafness. Transmission is autosomal recessive.	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
andre sygdomme i neurohypofysen	Finding site	False	Neurohypophysis structure	Inferred relationship	Some
anden sygdom i neurohypofysen, ikke nærmere specificeret	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
medikamentelt fremkaldt diabetes insipidus nephrogenica	Finding site	False	Neurohypophysis structure	Inferred relationship	Some	2
Acquired vasopressin resistance	Finding site	False	Neurohypophysis structure	Inferred relationship	Some	2
struktur af infundibulum hypophysis	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' syndrom	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
hereditær nefrogen diabetes insipidus	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

Reference Sets

Anatomy structure and entire association reference set (foundation metadata concept)

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Id	Description	Lang	Type	Status	Case?	Module
62564015	Pituitary posterior lobe	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
62565019	Neurohypophysis	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
486735016	Neurohypophysis structure	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
769388012	Neurohypophysis structure (body structure)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
1229321016	Posterior lobe of pituitary	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
2647001018	Pars nervosa of pituitary gland	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
2676571000005112	Neurohypofysen	da	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	Danish module (core metadata concept)