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254255007: Congenital malformation of anterior pituitary (disorder)


Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2014. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
378485013 Congenital malformation of anterior pituitary en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
645121011 Congenital malformation of anterior pituitary (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3006583014 Congenital anomaly of anterior pituitary en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
378485013 Congenital malformation of anterior pituitary en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
378485013 Congenital malformation of anterior pituitary en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
645121011 Congenital malformation of anterior pituitary (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
645121011 Congenital malformation of anterior pituitary (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3006583014 Congenital anomaly of anterior pituitary en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3006583014 Congenital anomaly of anterior pituitary en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5083141000241110 malformation congénitale de l'hypophyse antérieure fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5083141000241110 malformation congénitale de l'hypophyse antérieure fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


2 descendants. Search Descendants:

Expanded Value Set


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

Inbound Relationships Type Active Source Characteristic Refinability Group
Short stature-pituitary and cerebellar defects-small sella turcica syndrome is characterized by short stature, anterior pituitary hormone deficiency, small sella turcica, and a hypoplastic anterior hypophysis associated with pointed cerebellar tonsils. It has been described in three generations of a large French kindred. Ectopia of the posterior hypophysis was observed in some patients. The syndrome is transmitted as a dominantly inherited trait and is caused by a germline mutation within the LIM-homeobox transcription factor LHX4 gene (1q25). Is a True Congenital malformation of anterior pituitary Inferred relationship Existential restriction modifier (core metadata concept)
This syndrome is characterized by the association of intellectual deficit, congenital cataract, and hypogonadotropic hypogonadism. Is a True Congenital malformation of anterior pituitary Inferred relationship Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

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