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722944006: Congenital hypogonadotropic hypogonadism (disorder)


Status: current, Defined. 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 Case insensitive SNOMED CT core
3334001015 Congenital hypogonadotropic hypogonadism en Synonym Active Case insensitive SNOMED CT core


18 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital hypogonadotropic hypogonadism Is a Hypogonadotropic hypogonadism true Inferred relationship Some
Congenital hypogonadotropic hypogonadism Is a Congenital disease true Inferred relationship Some
Congenital hypogonadotropic hypogonadism Occurrence Congenital true Inferred relationship Some 2
Congenital hypogonadotropic hypogonadism Occurrence Congenital true Inferred relationship Some 3
Congenital hypogonadotropic hypogonadism Finding site Gonadal endocrine structure true Inferred relationship Some 2
Congenital hypogonadotropic hypogonadism Finding site Structure of distal part of pituitary true Inferred relationship Some 3

Inbound Relationships Type Active Source Characteristic Refinability Group
Hypogonadotropic hypogonadism, severe microcephaly, sensorineural hearing loss, dysmorphism syndrome Is a True Congenital hypogonadotropic hypogonadism Inferred relationship Some
Familial adrenal hypoplasia with absent pituitary luteinising hormone Is a True Congenital hypogonadotropic hypogonadism Inferred relationship Some
Obesity due to leptin receptor gene deficiency Is a True Congenital hypogonadotropic hypogonadism Inferred relationship Some
Prader-Willi syndrome Is a True Congenital hypogonadotropic hypogonadism Inferred relationship Some
Intellectual disability, myopathy, short stature, endocrine defect syndrome Is a True Congenital hypogonadotropic hypogonadism Inferred relationship Some
Congenital leptin deficiency Is a True Congenital hypogonadotropic hypogonadism Inferred relationship Some
Moebius syndrome, axonal neuropathy, hypogonadotropic hypogonadism syndrome Is a True Congenital hypogonadotropic hypogonadism Inferred relationship Some
Hyposmia, nasal and ocular hypoplasia, hypogonadotropic hypogonadism syndrome Is a True Congenital hypogonadotropic hypogonadism Inferred relationship Some
Hypogonadotropic hypogonadism retinitis pigmentosa syndrome Is a True Congenital hypogonadotropic hypogonadism Inferred relationship Some
Hypogonadism with anosmia Is a True Congenital hypogonadotropic hypogonadism Inferred relationship Some
Hypogonadotropic hypogonadism with frontoparietal alopecia syndrome Is a True Congenital hypogonadotropic hypogonadism Inferred relationship Some
Hypomyelination, hypogonadotropic hypogonadism, hypodontia syndrome Is a False Congenital hypogonadotropic hypogonadism Inferred relationship Some
Congenital cataract with intellectual disability and hypogonadotropic hypogonadism syndrome Is a True Congenital hypogonadotropic hypogonadism Inferred relationship Some
Prader-Willi-like syndrome Is a True Congenital hypogonadotropic hypogonadism Inferred relationship Some
Alopecia, progressive neurological defect, endocrinopathy syndrome Is a True Congenital hypogonadotropic hypogonadism Inferred relationship Some

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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