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718193005: Peripheral resistance to thyroid hormone (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2016. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3311452015 Peripheral resistance to thyroid hormone (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3311453013 Peripheral resistance to thyroid hormone en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3311452015 Peripheral resistance to thyroid hormone (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3311452015 Peripheral resistance to thyroid hormone (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3311453013 Peripheral resistance to thyroid hormone en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3311453013 Peripheral resistance to thyroid hormone en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3311454019 A permanent thyroid hormone deficiency that is present from birth. The majority of cases are asymptomatic but some may have features of hypothyroidism including decreased activity and increased sleep, feeding difficulty and constipation, prolonged jaundice, myxedematous facies, large fontanelles (especially posterior), macroglossia, a distended abdomen with umbilical hernia, and hypotonia. In 90% of cases the peripheral resistance to thyroid hormones is caused by dominantly inherited mutations in genes encoding for thyroid hormone receptor beta. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3311455018 A permanent thyroid hormone deficiency that is present from birth. The majority of cases are asymptomatic but some may have features of hypothyroidism including decreased activity and increased sleep, feeding difficulty and constipation, prolonged jaundice, myxoedematous facies, large fontanelles (especially posterior), macroglossia, a distended abdomen with umbilical hernia, and hypotonia. In 90% of cases the peripheral resistance to thyroid hormones is caused by dominantly inherited mutations in genes encoding for thyroid hormone receptor beta. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
986501000172110 résistance périphérique aux hormones thyroïdiennes fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
986501000172110 résistance périphérique aux hormones thyroïdiennes fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Peripheral resistance to thyroid hormone (disorder) Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Peripheral resistance to thyroid hormone (disorder) Is a Thyroid hormone responsiveness defect true Inferred relationship Existential restriction modifier (core metadata concept)
Peripheral resistance to thyroid hormone (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Peripheral resistance to thyroid hormone (disorder) Finding site Thyroid structure false Inferred relationship Existential restriction modifier (core metadata concept)
Peripheral resistance to thyroid hormone (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Peripheral resistance to thyroid hormone (disorder) Finding site Thyroid structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Inbound Relationships Type Active Source Characteristic Refinability Group
Congenital hypothyroidism due to peripheral resistance to thyroid hormone Due to True Peripheral resistance to thyroid hormone (disorder) Inferred relationship Existential restriction modifier (core metadata concept) 3

This concept is not in any reference sets

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