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722944006: hypogonadisme hypogonadotrope congénital (trouble)


Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2017. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3334000019 Congenital hypogonadotropic hypogonadism (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3334001015 Congenital hypogonadotropic hypogonadism en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
758951000241113 hypogonadisme hypogonadotrope congénital (trouble) fr Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
869451000172110 hypogonadisme hypogonadotrope congénital fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)


17 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital hypogonadotropic hypogonadism (disorder) est un(e) (attribut) hypogonadisme hypogonadotrope (trouble) true Inferred relationship Some
Congenital hypogonadotropic hypogonadism (disorder) est un(e) (attribut) Congenital disease true Inferred relationship Some
Congenital hypogonadotropic hypogonadism (disorder) survenue (attribut) congénital true Inferred relationship Some 2
Congenital hypogonadotropic hypogonadism (disorder) survenue (attribut) congénital true Inferred relationship Some 3
Congenital hypogonadotropic hypogonadism (disorder) localisation d'une constatation (attribut) Gonadal endocrine structure true Inferred relationship Some 2
Congenital hypogonadotropic hypogonadism (disorder) localisation d'une constatation (attribut) Structure of pars distalis of pituitary (body structure) true Inferred relationship Some 3

Inbound Relationships Type Active Source Characteristic Refinability Group
syndrome d'hypogonadisme hypogonadotrope-microcéphalie sévère-surdité neurosensorielle-dysmorphie est un(e) (attribut) True Congenital hypogonadotropic hypogonadism (disorder) Inferred relationship Some
Familial adrenal hypoplasia with absent pituitary luteinizing hormone (disorder) est un(e) (attribut) True Congenital hypogonadotropic hypogonadism (disorder) Inferred relationship Some
Obesity due to leptin receptor gene deficiency est un(e) (attribut) True Congenital hypogonadotropic hypogonadism (disorder) Inferred relationship Some
Prader-Willi syndrome est un(e) (attribut) True Congenital hypogonadotropic hypogonadism (disorder) Inferred relationship Some
Intellectual disability, myopathy, short stature, endocrine defect syndrome est un(e) (attribut) True Congenital hypogonadotropic hypogonadism (disorder) Inferred relationship Some
Moebius syndrome, axonal neuropathy, hypogonadotropic hypogonadism syndrome (disorder) est un(e) (attribut) True Congenital hypogonadotropic hypogonadism (disorder) Inferred relationship Some
syndrome d'hypoplasie nasale et oculaire-hypogonadisme hypogonadotrope est un(e) (attribut) True Congenital hypogonadotropic hypogonadism (disorder) Inferred relationship Some
Hypogonadotropic hypogonadism retinitis pigmentosa syndrome est un(e) (attribut) True Congenital hypogonadotropic hypogonadism (disorder) Inferred relationship Some
dysplasie olfactogénitale est un(e) (attribut) True Congenital hypogonadotropic hypogonadism (disorder) Inferred relationship Some
Hypogonadotropic hypogonadism with frontoparietal alopecia syndrome (disorder) est un(e) (attribut) True Congenital hypogonadotropic hypogonadism (disorder) Inferred relationship Some
Hypomyelination, hypogonadotropic hypogonadism, hypodontia syndrome (disorder) est un(e) (attribut) False Congenital hypogonadotropic hypogonadism (disorder) Inferred relationship Some
Congenital cataract with intellectual disability and hypogonadotropic hypogonadism syndrome (disorder) est un(e) (attribut) True Congenital hypogonadotropic hypogonadism (disorder) Inferred relationship Some
Prader-Willi-like syndrome est un(e) (attribut) True Congenital hypogonadotropic hypogonadism (disorder) Inferred relationship Some
Alopecia, progressive neurological defect, endocrinopathy syndrome (disorder) est un(e) (attribut) True Congenital hypogonadotropic hypogonadism (disorder) Inferred relationship Some

This concept is not in any reference sets

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