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771510006: X-linked central congenital hypothyroidism with late-onset testicular enlargement (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2019. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3706553013 X-linked central congenital hypothyroidism with late-onset testicular enlargement (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
3706554019 IGSF1 (immunoglobulin superfamily member 1) deficiency syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3706555018 X-linked central congenital hypothyroidism with late-onset macroorchidism en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3706556017 X-linked central congenital hypothyroidism with late-onset testicular enlargement en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3706557014 A rare genetic endocrine disease with characteristics of central hypothyroidism, testis enlargement in adolescence resulting in adult macroorchidism, delayed pubertal testosterone rise with a subsequent delayed pubertal growth spurt, small thyroid gland, and variable prolactin and growth hormone deficiency. Caused by mutation in the IGSF1 gene on chromosome Xq26. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3706553013 X-linked central congenital hypothyroidism with late-onset testicular enlargement (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
3706554019 IGSF1 (immunoglobulin superfamily member 1) deficiency syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3706555018 X-linked central congenital hypothyroidism with late-onset macroorchidism en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3706556017 X-linked central congenital hypothyroidism with late-onset testicular enlargement en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3706557014 A rare genetic endocrine disease with characteristics of central hypothyroidism, testis enlargement in adolescence resulting in adult macroorchidism, delayed pubertal testosterone rise with a subsequent delayed pubertal growth spurt, small thyroid gland, and variable prolactin and growth hormone deficiency. Caused by mutation in the IGSF1 gene on chromosome Xq26. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
1052961000195114 X-chromosomale kongenitale zentrale Hypothyreose mit spät-beginnender testikulärer Vergrösserung de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
895481000172117 hypothyroïdie congénitale centrale avec macroorchidie tardive liée à l'X fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
955521000172117 syndrome par déficit en IGSF1 fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
895481000172117 hypothyroïdie congénitale centrale avec macroorchidie tardive liée à l'X fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
955521000172117 syndrome par déficit en IGSF1 fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
1052961000195114 X-chromosomale kongenitale zentrale Hypothyreose mit spät-beginnender testikulärer Vergrösserung de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3397351001000119 X-chromosomale kongenitale zentrale Hypothyreose mit spät-beginnender testikulärer Vergrößerung 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
X-linked central congenital hypothyroidism with late-onset testicular enlargement (disorder) Associated morphology Hypertrophy true Inferred relationship Existential restriction modifier (core metadata concept) 1
X-linked central congenital hypothyroidism with late-onset testicular enlargement (disorder) Finding site Thyroid structure true Inferred relationship Existential restriction modifier (core metadata concept) 2
X-linked central congenital hypothyroidism with late-onset testicular enlargement (disorder) Is a Reproductive system hereditary disorder (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
X-linked central congenital hypothyroidism with late-onset testicular enlargement (disorder) Occurrence Adolescence (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
X-linked central congenital hypothyroidism with late-onset testicular enlargement (disorder) Is a Central hypothyroidism true Inferred relationship Existential restriction modifier (core metadata concept)
X-linked central congenital hypothyroidism with late-onset testicular enlargement (disorder) Is a X-linked hereditary disease false Inferred relationship Existential restriction modifier (core metadata concept)
X-linked central congenital hypothyroidism with late-onset testicular enlargement (disorder) Finding site Testis structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
X-linked central congenital hypothyroidism with late-onset testicular enlargement (disorder) Is a Hypertrophy of testis true Inferred relationship Existential restriction modifier (core metadata concept)
X-linked central congenital hypothyroidism with late-onset testicular enlargement (disorder) Is a Hereditary disorder of endocrine system (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
X-linked central congenital hypothyroidism with late-onset testicular enlargement (disorder) Is a X-linked recessive hereditary disease true Inferred relationship Existential restriction modifier (core metadata concept)

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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