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74012004: Congenital anomaly of pituitary gland (disorder)


Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
122900019 Congenital anomaly of pituitary gland en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
814465010 Congenital anomaly of pituitary gland (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
1233691019 Congenital malformation of pituitary gland en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
122900019 Congenital anomaly of pituitary gland en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
122900019 Congenital anomaly of pituitary gland en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
814465010 Congenital anomaly of pituitary gland (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
814465010 Congenital anomaly of pituitary gland (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
1233691019 Congenital malformation of pituitary gland en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1233691019 Congenital malformation of pituitary gland en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
4632371000241117 anomalie congénitale de la glande pituitaire fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
4632371000241117 anomalie congénitale de la glande pituitaire fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


12 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital anomaly of pituitary gland Is a Ear, face and neck congenital anomalies (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital anomaly of pituitary gland Is a Congenital anomaly of endocrine gland true Inferred relationship Existential restriction modifier (core metadata concept)
Congenital anomaly of pituitary gland Is a Disease of pituitary gland false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital anomaly of pituitary gland Is a Congenital anomaly of head false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital anomaly of pituitary gland Associated morphology Congenital malformation false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital anomaly of pituitary gland Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital anomaly of pituitary gland Finding site Pituitary structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital anomaly of pituitary gland Finding site Entire endocrine gonad (body structure) false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital anomaly of pituitary gland Is a Disorder of pituitary gland (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Congenital anomaly of pituitary gland Is a Congenital anomaly of brain false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital anomaly of pituitary gland Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital anomaly of pituitary gland Finding site Pituitary structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital anomaly of pituitary gland Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital anomaly of pituitary gland Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital anomaly of pituitary gland Associated morphology anomalie du développement false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital anomaly of pituitary gland Finding site Pituitary structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital anomaly of pituitary gland Is a Anomalies of hypothalamus (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital anomaly of pituitary gland Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital anomaly of pituitary gland Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital anomaly of pituitary gland Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital anomaly of pituitary gland Is a Congenital anomaly of cerebrum (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)

Inbound Relationships Type Active Source Characteristic Refinability Group
Congenital absence of pituitary gland Is a True Congenital anomaly of pituitary gland Inferred relationship Existential restriction modifier (core metadata concept)
Accessory pituitary gland Is a True Congenital anomaly of pituitary gland Inferred relationship Existential restriction modifier (core metadata concept)
Congenital malformation of anterior pituitary Is a True Congenital anomaly of pituitary gland Inferred relationship Existential restriction modifier (core metadata concept)
Congenital malformation of posterior pituitary Is a True Congenital anomaly of pituitary gland Inferred relationship Existential restriction modifier (core metadata concept)
Ectopic pituitary tissue Is a True Congenital anomaly of pituitary gland Inferred relationship Existential restriction modifier (core metadata concept)
Anomaly of pituitary gland NOS Is a False Congenital anomaly of pituitary gland Inferred relationship Existential restriction modifier (core metadata concept)
Beckwith-Wiedemann syndrome (disorder) Is a False Congenital anomaly of pituitary gland Inferred relationship Existential restriction modifier (core metadata concept)
Thyrotoxicosis due to pituitary thyroid hormone resistance Is a False Congenital anomaly of pituitary gland Inferred relationship Existential restriction modifier (core metadata concept)
Rathke's pouch cyst Is a True Congenital anomaly of pituitary gland Inferred relationship Existential restriction modifier (core metadata concept)
Sotos' syndrome Is a False Congenital anomaly of pituitary gland Inferred relationship Existential restriction modifier (core metadata concept)
Schwartz syndrome Is a False Congenital anomaly of pituitary gland Inferred relationship Existential restriction modifier (core metadata concept)
Hypogonadism with anosmia Is a False Congenital anomaly of pituitary gland Inferred relationship Existential restriction modifier (core metadata concept)
Hypohidrosis-diabetes insipidus syndrome Is a False Congenital anomaly of pituitary gland Inferred relationship Existential restriction modifier (core metadata concept)
Pituitary stalk interruption syndrome (PSIS) is a congenital abnormality of the pituitary that is responsible for pituitary deficiency and is usually characterized by the triad of a very thin or interrupted pituitary stalk, an ectopic (or absent) posterior pituitary (EPP) and hypoplasia or aplasia of the anterior pituitary visible on MRI. In some patients the abnormality may be limited to EPP (also called ectopic neurohypophysis) or to an interrupted pituitary stalk. Is a True Congenital anomaly of pituitary gland Inferred relationship Existential restriction modifier (core metadata concept)
Hypothyroidism due to mutations in transcription factors involved in pituitary development or function is a type of central congenital hypothyroidism, a permanent thyroid deficiency that is present from birth, characterized by low levels of thyroid hormones caused by disorders in the development or function of the pituitary. Due to True Congenital anomaly of pituitary gland Inferred relationship Existential restriction modifier (core metadata concept) 2
Septo-optic dysplasia sequence Is a True Congenital anomaly of pituitary gland Inferred relationship Existential restriction modifier (core metadata concept)

Reference Sets

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