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70348004: Pendred's syndrome (disorder)


Status: current, Not 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
116846019 Pendred's syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
116847011 Hypothyroidism with sensorineural deafness en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
116848018 Thyroid hormone organification defect II B en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
116849014 Goiter-deafness syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
116850014 Genetic defect in thyroid hormonogenesis II B en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
116851013 GDTH IIB en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
116852018 Goitre-deafness syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
810394014 Pendred's syndrome (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
1233257013 Pendred syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
116846019 Pendred's syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
116847011 Hypothyroidism with sensorineural deafness en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
116847011 Hypothyroidism with sensorineural deafness en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
116848018 Thyroid hormone organification defect II B en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
116849014 Goiter-deafness syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
116849014 Goiter-deafness syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
116850014 Genetic defect in thyroid hormonogenesis II B en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
116851013 GDTH IIB en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
116852018 Goitre-deafness syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
116852018 Goitre-deafness syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
810394014 Pendred's syndrome (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
810394014 Pendred's syndrome (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
1233257013 Pendred syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1233257013 Pendred syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3391481001000113 Pendred-Syndrom de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
886581000172113 syndrome de Pendred fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
987271000172115 syndrome de goitre-surdité fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
886581000172113 syndrome de Pendred fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
987271000172115 syndrome de goitre-surdité fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3391481001000113 Pendred-Syndrom de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Pendred's syndrome Is a Dyshormonogenic goiter false Inferred relationship Existential restriction modifier (core metadata concept)
Pendred's syndrome Is a Inherited disorder of thyroid metabolism true Inferred relationship Existential restriction modifier (core metadata concept)
Pendred's syndrome Finding site Entire endocrine gonad (body structure) false Inferred relationship Existential restriction modifier (core metadata concept)
Pendred's syndrome Finding site Thyroid structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Pendred's syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Pendred's syndrome Associated morphology Hyperplasia false Inferred relationship Existential restriction modifier (core metadata concept) 1
Pendred's syndrome Finding site Thyroid structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Pendred's syndrome Associated morphology Hyperplasia false Inferred relationship Existential restriction modifier (core metadata concept) 1
Pendred's syndrome Associated morphology Enlargement (morphologic abnormality) true Inferred relationship Existential restriction modifier (core metadata concept) 2
Pendred's syndrome Finding site Entire thyroid gland true Inferred relationship Existential restriction modifier (core metadata concept) 2
Pendred's syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Pendred's syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 2
Pendred's syndrome Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Pendred's syndrome Is a goitre euthyroïdien false Inferred relationship Existential restriction modifier (core metadata concept)
Pendred's syndrome Is a Congenital sensorineural hearing loss (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Pendred's syndrome Is a Auditory system hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Pendred's syndrome Finding site Entire thyroid gland false Inferred relationship Existential restriction modifier (core metadata concept) 1
Pendred's syndrome Associated morphology Enlargement (morphologic abnormality) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Pendred's syndrome Interprets Hearing true Inferred relationship Existential restriction modifier (core metadata concept) 3
Pendred's syndrome Finding site Structure of auditory system (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 2
Pendred's syndrome Is a Goiter true Inferred relationship Existential restriction modifier (core metadata concept)
Pendred's syndrome Is a Congenital anomaly of ear with impairment of hearing true Inferred relationship Existential restriction modifier (core metadata concept)
Pendred's syndrome Associated morphology anomalie du développement false Inferred relationship Existential restriction modifier (core metadata concept) 1
Pendred's syndrome Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Pendred's syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 4
Pendred's syndrome Finding site Thyroid structure true Inferred relationship Existential restriction modifier (core metadata concept) 4
Pendred's syndrome Finding site Structure of vestibular apparatus (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Pendred's syndrome Is a Developmental hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Pendred's syndrome Is a Congenital anomaly of vestibule of inner ear true Inferred relationship Existential restriction modifier (core metadata concept)
Pendred's syndrome Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier (core metadata concept) 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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