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733113002: Hypogonadotropic hypogonadism retinitis pigmentosa syndrome (disorder)


Status: current, Primitive. Date: 31-Jul 2017. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3498781017 Hypogonadotropic hypogonadism retinitis pigmentosa syndrome en Synonym Active Case insensitive SNOMED CT core
3498782012 Chang Davidson Carlson syndrome en Synonym Active Case sensitive SNOMED CT core
3498783019 Hypogonadotropic hypogonadism retinitis pigmentosa syndrome (disorder) en Fully specified name Active Case insensitive SNOMED CT core
3499981015 This syndrome is characterized by the association of hypogonadotropic hypogonadism (with primary amenorrhea and lack of secondary sexual development) and retinitis pigmentosa. It has been described in two sisters born to nonconsanguineous parents. en Definition Active Case sensitive SNOMED CT core
3499982010 This syndrome is characterised by the association of hypogonadotropic hypogonadism (with primary amenorrhoea and lack of secondary sexual development) and retinitis pigmentosa. It has been described in two sisters born to nonconsanguineous parents. en Definition Active Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hypogonadotropic hypogonadism retinitis pigmentosa syndrome Is a Retinitis pigmentosa true Inferred relationship Some
Hypogonadotropic hypogonadism retinitis pigmentosa syndrome Is a Hereditary disorder of endocrine system true Inferred relationship Some
Hypogonadotropic hypogonadism retinitis pigmentosa syndrome Is a Hereditary disorder of nervous system true Inferred relationship Some
Hypogonadotropic hypogonadism retinitis pigmentosa syndrome Is a Reproductive system hereditary disorder true Inferred relationship Some
Hypogonadotropic hypogonadism retinitis pigmentosa syndrome Is a Congenital hypogonadotropic hypogonadism true Inferred relationship Some
Hypogonadotropic hypogonadism retinitis pigmentosa syndrome Associated morphology Dystrophy true Inferred relationship Some 3
Hypogonadotropic hypogonadism retinitis pigmentosa syndrome Occurrence Congenital true Inferred relationship Some 3
Hypogonadotropic hypogonadism retinitis pigmentosa syndrome Finding site Retinal structure true Inferred relationship Some 3
Hypogonadotropic hypogonadism retinitis pigmentosa syndrome Occurrence Congenital true Inferred relationship Some 4
Hypogonadotropic hypogonadism retinitis pigmentosa syndrome Occurrence Congenital true Inferred relationship Some 5
Hypogonadotropic hypogonadism retinitis pigmentosa syndrome Finding site Gonadal endocrine structure true Inferred relationship Some 4
Hypogonadotropic hypogonadism retinitis pigmentosa syndrome Finding site Structure of distal part of pituitary true Inferred relationship Some 5

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

Description inactivation indicator reference set

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