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783549006: Obesity due to centrosomal protein 19 deficiency (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2019. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3759295011 Obesity due to centrosomal protein 19 deficiency en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3759296012 Obesity due to CEP19 deficiency en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3759297015 Obesity due to centrosomal protein 19 deficiency (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3759298013 A rare genetic form of obesity characterised by morbid obesity, hypertension, type 2 diabetes mellitus and dyslipidaemia leading to early coronary disease, myocardial infarction and congestive heart failure. Intellectual disability and decreased sperm counts or azoospermia have also been reported. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3759299017 A rare genetic form of obesity characterized by morbid obesity, hypertension, type 2 diabetes mellitus and dyslipidemia leading to early coronary disease, myocardial infarction and congestive heart failure. Intellectual disability and decreased sperm counts or azoospermia have also been reported. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3759295011 Obesity due to centrosomal protein 19 deficiency en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3759296012 Obesity due to CEP19 deficiency en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3759297015 Obesity due to centrosomal protein 19 deficiency (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3759298013 A rare genetic form of obesity characterised by morbid obesity, hypertension, type 2 diabetes mellitus and dyslipidaemia leading to early coronary disease, myocardial infarction and congestive heart failure. Intellectual disability and decreased sperm counts or azoospermia have also been reported. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3759299017 A rare genetic form of obesity characterized by morbid obesity, hypertension, type 2 diabetes mellitus and dyslipidemia leading to early coronary disease, myocardial infarction and congestive heart failure. Intellectual disability and decreased sperm counts or azoospermia have also been reported. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3382361001000119 Adipositas durch CEP19-Mangel de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6407391000241115 obésité due à un déficit en CEP19 (centrosomal protein 19) fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6407391000241115 obésité due à un déficit en CEP19 (centrosomal protein 19) fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3382361001000119 Adipositas durch CEP19-Mangel de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Obesity due to CEP19 deficiency Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Obesity due to CEP19 deficiency Is a Morbid obesity (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Obesity due to CEP19 deficiency Interprets Measured body weight (observable entity) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Obesity due to CEP19 deficiency Has interpretation Above reference range true Inferred relationship Existential restriction modifier (core metadata concept) 1
Obesity due to CEP19 deficiency Is a Genetic non-syndromic obesity true Inferred relationship Existential restriction modifier (core metadata concept)
Obesity due to CEP19 deficiency Occurrence Childhood true Inferred relationship Existential restriction modifier (core metadata concept) 2
Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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