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70348004: Pendred's syndrome (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
116846019 Pendred's syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
116847011 Hypothyroidism with sensorineural deafness en Synonym Active Entire term case insensitive SNOMED CT core module
116848018 Thyroid hormone organification defect II B en Synonym Active Only initial character case insensitive SNOMED CT core module
116849014 Goiter-deafness syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
116850014 Genetic defect in thyroid hormonogenesis II B en Synonym Active Only initial character case insensitive SNOMED CT core module
116851013 GDTH IIB en Synonym Active Entire term case sensitive SNOMED CT core module
116852018 Goitre-deafness syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
810394014 Pendred's syndrome (disorder) en Fully specified name Active Entire term case sensitive SNOMED CT core module
1233257013 Pendred syndrome en Synonym Active Entire term case sensitive SNOMED CT core 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
Pendred's syndrome Is a Inherited disorder of thyroid metabolism true Inferred relationship Existential restriction modifier
Pendred's syndrome Finding site Entire endocrine gonad false Inferred relationship Existential restriction modifier
Pendred's syndrome Finding site Thyroid structure false Inferred relationship Existential restriction modifier 1
Pendred's syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier
Pendred's syndrome Associated morphology Hyperplasia false Inferred relationship Existential restriction modifier 1
Pendred's syndrome Finding site Thyroid structure false Inferred relationship Existential restriction modifier 1
Pendred's syndrome Associated morphology Hyperplasia false Inferred relationship Existential restriction modifier 1
Pendred's syndrome Associated morphology Enlargement true Inferred relationship Existential restriction modifier 2
Pendred's syndrome Finding site Entire thyroid gland true Inferred relationship Existential restriction modifier 2
Pendred's syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Pendred's syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier 2
Pendred's syndrome Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier
Pendred's syndrome Is a Euthyroid goiter false Inferred relationship Existential restriction modifier
Pendred's syndrome Is a Congenital sensorineural hearing loss true Inferred relationship Existential restriction modifier
Pendred's syndrome Is a Auditory system hereditary disorder true Inferred relationship Existential restriction modifier
Pendred's syndrome Finding site Entire thyroid gland false Inferred relationship Existential restriction modifier 1
Pendred's syndrome Associated morphology Enlargement false Inferred relationship Existential restriction modifier 1
Pendred's syndrome Interprets Hearing, function true Inferred relationship Existential restriction modifier 3
Pendred's syndrome Finding site Structure of auditory system false Inferred relationship Existential restriction modifier 2
Pendred's syndrome Is a Goiter true Inferred relationship Existential restriction modifier
Pendred's syndrome Is a Congenital anomaly of ear with impairment of hearing true Inferred relationship Existential restriction modifier
Pendred's syndrome Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 1
Pendred's syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Pendred's syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 4
Pendred's syndrome Finding site Thyroid structure true Inferred relationship Existential restriction modifier 4
Pendred's syndrome Finding site Structure of vestibular apparatus true Inferred relationship Existential restriction modifier 1
Pendred's syndrome Is a Developmental hereditary disorder true Inferred relationship Existential restriction modifier
Pendred's syndrome Is a Congenital anomaly of vestibule of inner ear true Inferred relationship Existential restriction modifier
Pendred's syndrome Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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