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783549006: obesitas door deficiëntie van 'centrosomal protein 19' (aandoening)


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
9966991000146110 obesitas door CEP19-deficiëntie nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
10755781000146117 obesitas door deficiëntie van 'centrosomal protein 19' (aandoening) nl Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
10755791000146115 obesitas door deficiëntie van 'centrosomal protein 19' nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
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


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 Some
Obesity due to CEP19 deficiency Is a Morbid obesity true Inferred relationship Some
Obesity due to CEP19 deficiency Interprets Body weight measure true Inferred relationship Some 1
Obesity due to CEP19 deficiency Has interpretation Above reference range true Inferred relationship Some 1
Obesity due to CEP19 deficiency Is a Genetic non-syndromic obesity (disorder) true Inferred relationship Some
Obesity due to CEP19 deficiency Occurrence Childhood true Inferred relationship Some 2

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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