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1359763002: Genetic syndromic childhood obesity (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 01-Apr 2025. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
5436515012 Childhood onset obesity associated with a genetic syndrome. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5436512010 Genetic syndromic childhood obesity en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5436513017 Genetic syndromic childhood obesity (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

10 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Childhood onset obesity associated with a genetic syndrome. Is a Childhood obesity due to genetic disease. true Inferred relationship Some
Childhood onset obesity associated with a genetic syndrome. Occurrence Childhood true Inferred relationship Some 2
Childhood onset obesity associated with a genetic syndrome. Interprets Measured body weight (observable entity) true Inferred relationship Some 1
Childhood onset obesity associated with a genetic syndrome. Has interpretation Above reference range true Inferred relationship Some 1
Inbound Relationships Type Active Source Characteristic Refinability Group
Pseudohypoparathyroidism type I A Is a True Childhood onset obesity associated with a genetic syndrome. Inferred relationship Some
Alstrom syndrome Is a True Childhood onset obesity associated with a genetic syndrome. Inferred relationship Some
Bardet-Biedl syndrome Is a True Childhood onset obesity associated with a genetic syndrome. Inferred relationship Some
A rare syndromic craniosynostosis with variable phenotypic expression characterized by craniosynostosis, intellectual disability, distinctive facies, abnormalities of the fingers and toes (brachydactyly, polydactyly and syndactyly), short stature, congenital heart disease, skeletal defects, obesity, genital abnormalities and umbilical hernia. Is a True Childhood onset obesity associated with a genetic syndrome. Inferred relationship Some
Intellectual disability-seizures-macrocephaly-obesity syndrome is a rare syndromic obesity due to complex chromosomal rearrangement characterized by development delay and intellectual disability, childhood-onset obesity, seizures, poor coordination and broad-based gait, macrocephaly and mild dysmorphic features (such as narrow palpebral fissures, malar hypoplasia and thin upper lips), eczema, ocular abnormalities and a social personality. Is a True Childhood onset obesity associated with a genetic syndrome. Inferred relationship Some
Cohen syndrome Is a True Childhood onset obesity associated with a genetic syndrome. Inferred relationship Some
Prader-Willi syndrome Is a True Childhood onset obesity associated with a genetic syndrome. Inferred relationship Some
A rare syndromic endocrine disease characterized by childhood-onset hyperphagia and obesity, alveolar hypoventilation, dysautonomia, hypothalamic dysfunction and neurobehavioral disorders. Central hypothyroidism, endocrine anomalies, electrolyte imbalances and respiratory failure may also be associated. Is a True Childhood onset obesity associated with a genetic syndrome. Inferred relationship Some
A rare Prader-Willi-like syndrome characterized by severe obesity due to SIM1 mutation, in addition to some clinical features of Prader-Willi- syndrome including intellectual disability, developmental delay, behavior problems and facial dysmorphism. Unlike Prader-Willi syndrome, short stature, hypotonia and hypogonadism may not be observed. Is a True Childhood onset obesity associated with a genetic syndrome. Inferred relationship Some
A rare genetic multiple congenital anomalies/dysmorphic syndrome characterized by global developmental delay, intellectual disability, short stature, skeletal abnormalities (such as brachydactyly and vertebral anomalies), obesity, cardiac, respiratory, and genitourinary anomalies, and dysmorphic facial features (including coarse facies, thick eyebrows, synophrys, hypertelorism, short, upturned nose, and long philtrum). Additional reported manifestations are microcephaly, hearing impairment, cataract, and gastroesophageal reflux. Is a True Childhood onset obesity associated with a genetic syndrome. Inferred relationship Some

This concept is not in any reference sets

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