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700150001: Congenital leptin deficiency (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2014. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
2989311014 Congenital leptin deficiency en Synonym Active Entire term case insensitive SNOMED CT core module
2989546019 Congenital leptin deficiency (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
5159491011 Obesity due to congenital leptin deficiency en Synonym Active Entire term case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital leptin deficiency Is a Congenital disease false Inferred relationship Existential restriction modifier
Congenital leptin deficiency Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Congenital leptin deficiency Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier
Congenital leptin deficiency Is a Genetic non-syndromic obesity true Inferred relationship Existential restriction modifier
Congenital leptin deficiency Is a Hereditary disorder of endocrine system true Inferred relationship Existential restriction modifier
Congenital leptin deficiency Is a Hereditary disorder of nervous system true Inferred relationship Existential restriction modifier
Congenital leptin deficiency Is a Reproductive system hereditary disorder true Inferred relationship Existential restriction modifier
Congenital leptin deficiency Is a Congenital hypogonadotropic hypogonadism true Inferred relationship Existential restriction modifier
Congenital leptin deficiency Occurrence Childhood true Inferred relationship Existential restriction modifier 4
Congenital leptin deficiency Interprets Measured body weight true Inferred relationship Existential restriction modifier 3
Congenital leptin deficiency Has interpretation Above reference range true Inferred relationship Existential restriction modifier 3
Congenital leptin deficiency Finding site Gonadal endocrine structure true Inferred relationship Existential restriction modifier 1
Congenital leptin deficiency Occurrence Congenital true Inferred relationship Existential restriction modifier 2
Congenital leptin deficiency Finding site Structure of pars distalis of pituitary true Inferred relationship Existential restriction modifier 2

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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