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733113002: Hypogonadotropic hypogonadism retinitis pigmentosa syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2017. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3498781017 Hypogonadotropic hypogonadism retinitis pigmentosa syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
3498782012 Chang Davidson Carlson syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
3498783019 Hypogonadotropic hypogonadism retinitis pigmentosa syndrome (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module


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 Existential restriction modifier
Hypogonadotropic hypogonadism retinitis pigmentosa syndrome Is a Hereditary disorder of endocrine system true Inferred relationship Existential restriction modifier
Hypogonadotropic hypogonadism retinitis pigmentosa syndrome Is a Hereditary disorder of nervous system true Inferred relationship Existential restriction modifier
Hypogonadotropic hypogonadism retinitis pigmentosa syndrome Is a Reproductive system hereditary disorder true Inferred relationship Existential restriction modifier
Hypogonadotropic hypogonadism retinitis pigmentosa syndrome Is a Congenital hypogonadotropic hypogonadism true Inferred relationship Existential restriction modifier
Hypogonadotropic hypogonadism retinitis pigmentosa syndrome Associated morphology Dystrophy true Inferred relationship Existential restriction modifier 3
Hypogonadotropic hypogonadism retinitis pigmentosa syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 3
Hypogonadotropic hypogonadism retinitis pigmentosa syndrome Finding site Retinal structure true Inferred relationship Existential restriction modifier 3
Hypogonadotropic hypogonadism retinitis pigmentosa syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 4
Hypogonadotropic hypogonadism retinitis pigmentosa syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 5
Hypogonadotropic hypogonadism retinitis pigmentosa syndrome Finding site Gonadal endocrine structure true Inferred relationship Existential restriction modifier 4
Hypogonadotropic hypogonadism retinitis pigmentosa syndrome Finding site Structure of pars distalis of pituitary true Inferred relationship Existential restriction modifier 5

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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