414916001: Obesity (disorder)

SNOMED CT Concept\Clinical finding (finding)\...

\Body measurement finding\Weight finding\High body weight (finding)\Obese (finding)\Obesity (disorder)

\Disease\Obesity (disorder)

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2005. Module: SNOMED CT core

Descriptions:

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Obesity (disorder)	Is a	Disease	true	Inferred relationship	Some
Obesity (disorder)	Has definitional manifestation	Obese (finding)	false	Inferred relationship	Some
Obesity (disorder)	Interprets	Measured body weight (observable entity)	true	Inferred relationship	Some	1
Obesity (disorder)	Is a	Obese (finding)	true	Inferred relationship	Some
Obesity (disorder)	Has interpretation	Above reference range	true	Inferred relationship	Some	1

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Obesity by fat distribution pattern (disorder)	Is a	True	Obesity (disorder)	Inferred relationship	Some
obésité selon l'âge d'apparition	Is a	False	Obesity (disorder)	Inferred relationship	Some
Obesity by contributing factors (disorder)	Is a	True	Obesity (disorder)	Inferred relationship	Some
Obesity by adipocyte growth pattern (disorder)	Is a	True	Obesity (disorder)	Inferred relationship	Some
Simple obesity (disorder)	Is a	True	Obesity (disorder)	Inferred relationship	Some
gain pondéral excessif durant la grossesse	Is a	False	Obesity (disorder)	Inferred relationship	Some
Mauriac's syndrome	Is a	True	Obesity (disorder)	Inferred relationship	Some
Morbid obesity	Is a	True	Obesity (disorder)	Inferred relationship	Some
Weight-reducing diet education (procedure)	Has focus	False	Obesity (disorder)	Inferred relationship	Some
Obesity diet education (procedure)	Has focus	True	Obesity (disorder)	Inferred relationship	Some	2
Obesity associated disorder	Associated with	True	Obesity (disorder)	Inferred relationship	Some	1
FH: Obesity	Associated finding	False	Obesity (disorder)	Inferred relationship	Some	1
H/O: obesity	Associated finding	False	Obesity (disorder)	Inferred relationship	Some	1
Obesity screening	Has focus	True	Obesity (disorder)	Inferred relationship	Some	2
Weight loss advised	Has focus	False	Obesity (disorder)	Inferred relationship	Some
Drug-induced obesity	Is a	True	Obesity (disorder)	Inferred relationship	Some
H/O: obesity	Associated finding	True	Obesity (disorder)	Inferred relationship	Some	1
FH: Obesity	Associated finding	True	Obesity (disorder)	Inferred relationship	Some	1
FH: Obesity	Associated finding	False	Obesity (disorder)	Inferred relationship	Some	1
Obesity in mother complicating childbirth (disorder)	Is a	True	Obesity (disorder)	Inferred relationship	Some
Lymphedema associated with obesity (disorder)	Associated with	True	Obesity (disorder)	Inferred relationship	Some	1
Alstrom syndrome	Has definitional manifestation	False	Obesity (disorder)	Inferred relationship	Some
Severe obesity	Is a	True	Obesity (disorder)	Inferred relationship	Some
Melanocortin 4 receptor (MC4R) deficiency is the commonest form of monogenic obesity identified so far. MC4R deficiency is characterized by severe obesity, an increase in lean body mass and bone mineral density, increased linear growth in early childhood, hyperphagia beginning in the first year of life and severe hyperinsulinemia, in the presence of preserved reproductive function.	Is a	False	Obesity (disorder)	Inferred relationship	Some
A rare, X-linked syndromic intellectual disability disorder characterized by mild to moderate intellectual disability, obesity, hypogonadism, tapering fingers and microphallus with small or undescended testes, localized to Xp11.3-Xq23. Additional variable manifestations include alopecia, dental and eyesight anomalies, speech disabilities, and decreased body strength.	Is a	False	Obesity (disorder)	Inferred relationship	Some
X-linked intellectual disability with precocious puberty and obesity syndrome	Is a	False	Obesity (disorder)	Inferred relationship	Some
An X-linked retinal dystrophy characterized by choroideremia, causing in affected males progressive nyctalopia and eventual central blindness. Obesity, moderate intellectual disability and congenital mixed (sensorineural and conductive) deafness are also observed. Female carriers show typical retinal changes indicative of the choroideremia carrier state.	Is a	False	Obesity (disorder)	Inferred relationship	Some
Telehealth obesity monitoring (regime/therapy)	Has focus	True	Obesity (disorder)	Inferred relationship	Some	2
A rare X-linked syndromic intellectual disability characterized by mild to profound intellectual disability, microcephaly, growth delay, and hypogenitalism. Obesity, early-onset diabetes and epilepsy are more variably present.	Is a	False	Obesity (disorder)	Inferred relationship	Some
Obesity-colitis-hypothyroidism-cardiac hypertrophy-developmental delay syndrome is characterized by precocious obesity, congenital hypothyroidism, neonatal colitis, cardiac hypertrophy, craniosynostosis and developmental delay. It has been described in two brothers, one of whom died within the first month of life. The parents of the two children were nonconsanguineous and in good health, however, the pregnancies were complicated by a maternal HELLP syndrome (Haemolysis, Elevated Liver enzymes and Low Platelets). The mode of inheritance has not yet been clearly established.	Has definitional manifestation	False	Obesity (disorder)	Inferred relationship	Some
A rare genetic endocrine disease characterized by early onset of severe intractable diarrhea and intestinal malabsorption, followed by obesity and hormonal deficiencies due to insufficient activation of several prohormones, resulting in hypocortisolism, hypothyroidism, diabetes insipidus, hypogonadism, growth deficiency, and diabetes mellitus. Extent and age of onset of hormone deficiencies are variable between patients.	Is a	False	Obesity (disorder)	Inferred relationship	Some
Obesity caused by energy imbalance (disorder)	Is a	True	Obesity (disorder)	Inferred relationship	Some
MOMO syndrome is a very rare genetic overgrowth/obesity syndrome characterized by macrocephaly, obesity, mental (intellectual) disability and ocular abnormalities. Other frequent clinical signs include macrosomia, downslanting palpebral fissures, hypertelorism, broad nasal root, high and broad forehead and delay in bone maturation, in association with normal thyroid function and karyotype.	Is a	False	Obesity (disorder)	Inferred relationship	Some
Intellectual disability-obesity-brain malformations-facial dysmorphism syndrome is a rare, syndromic intellectual disability primarily characterized by moderate to severe intellectual disability, true-to-relative microcephaly and brain abnormalities including a thin corpus callosum, cerebellar hypoplasia, cerebral white matter hypoplasia and multi-focal hyperintensity of cerebral white matter on MRI. Obesity and distinctive craniofacial dysmorphism (including brachycephaly, round face, straight eyebrows, synophrys, hypertelorism, epicanthus, wide and depressed nasal bridge, protruding ears with uplifted lobe, downslanting corners of the mouth) are additional features.	Is a	False	Obesity (disorder)	Inferred relationship	Some
Alstrom syndrome	Is a	False	Obesity (disorder)	Inferred relationship	Some
Obesity-colitis-hypothyroidism-cardiac hypertrophy-developmental delay syndrome is characterized by precocious obesity, congenital hypothyroidism, neonatal colitis, cardiac hypertrophy, craniosynostosis and developmental delay. It has been described in two brothers, one of whom died within the first month of life. The parents of the two children were nonconsanguineous and in good health, however, the pregnancies were complicated by a maternal HELLP syndrome (Haemolysis, Elevated Liver enzymes and Low Platelets). The mode of inheritance has not yet been clearly established.	Is a	True	Obesity (disorder)	Inferred relationship	Some
A rare group of multiple congenital anomalies/dysmorphic syndrome characterised by autism spectrum disorder, developmental delay, intellectual disability, hyperphagia/obesity, and short stature (clinical features overlapping with Prader-Willi syndrome). However, it is a clinically and genetically heterogeneous group where patients may completely lack or manifests in minority some classical clinical features of Prader-Willi syndrome such as short stature, hypotonia, hypogonadism, hyperphagia and morbid obesity.	Is a	False	Obesity (disorder)	Inferred relationship	Some
Intellectual disability-obesity-prognathism-eye and skin anomalies syndrome is a rare, genetic, syndromic intellectual disability disorder characterized by mild to profound intellectual disability, delayed speech, obesity, ocular anomalies (blepharophimosis, blepharoptosis, hyperopic astigmatism, decreased visual acuity, strabismus, abducens nerve palsy, and/or accommodative esotropia), and dermal manifestations, such as chronic atopic dermatitis. Associated craniofacial dysmorphism includes macrocephaly, maxillary hypoplasia, mandibular prognathism, and crowding of teeth.	Is a	False	Obesity (disorder)	Inferred relationship	Some
Body mass index at or above 95th percentile as compared to children of the same age and sex	Is a	True	Obesity (disorder)	Inferred relationship	Some
Obesity in adolescence (disorder)	Is a	True	Obesity (disorder)	Inferred relationship	Some
Adult-onset obesity	Is a	True	Obesity (disorder)	Inferred relationship	Some
Lifelong obesity	Is a	True	Obesity (disorder)	Inferred relationship	Some
Fetal disorder due to maternal obesity (disorder)	Due to	True	Obesity (disorder)	Inferred relationship	Some	2
Fetal disorder due to maternal obesity with adult body mass index equal to or greater than 40	Due to	True	Obesity (disorder)	Inferred relationship	Some	1
Fetal disorder due to maternal obesity with adult body mass index 30 or greater but less than 40	Due to	True	Obesity (disorder)	Inferred relationship	Some	2
Maternal obesity complicating pregnancy, childbirth and the puerperium, antepartum	Is a	True	Obesity (disorder)	Inferred relationship	Some
Primary obesity surgery endoluminal 2 (procedure)	Has focus	True	Obesity (disorder)	Inferred relationship	Some	3
Disorder of spinal cord due to obesity (disorder)	Due to	True	Obesity (disorder)	Inferred relationship	Some	1
Benign intracranial hypertension due to obesity (disorder)	Due to	True	Obesity (disorder)	Inferred relationship	Some	3
Peripheral neuropathy due to obesity	Due to	True	Obesity (disorder)	Inferred relationship	Some	2
Neurological disorder due to obesity	Due to	True	Obesity (disorder)	Inferred relationship	Some	2
Neuropathy due to obesity	Due to	True	Obesity (disorder)	Inferred relationship	Some	2
Obesity due to pituitary disease	Is a	True	Obesity (disorder)	Inferred relationship	Some
A rare genetic multiple congenital anomalies/dysmorphic syndrome characterized by variable developmental delay and intellectual disability, overweight or obesity, behavioral abnormalities (including hyperactivity, aggressive behavior, anxiety, mood disorder, or autistic features), and facial dysmorphism (such as high forehead, full eyebrows and/or synophrys, upturned nose, and fleshy ears, among others). Additional reported manifestations are hypotonia, ocular anomalies, anomalies of the fingers and toes, joint hypermobility, or abnormal pigmentation. Brain imaging may show mild nonspecific abnormalities.	Is a	False	Obesity (disorder)	Inferred relationship	Some
X-linked intellectual disability-short stature-overweight syndrome is a multiple congenital anomalies syndrome characterised by borderline to severe intellectual disability, speech delay, short stature, elevated body mass index, a pattern of truncal obesity (reported in older males), and variable neurologic features (e.g. hypotonia, tremors, gait disturbances, behavioural problems, and seizure disorders). Less common manifestations include microcephaly, microorchidism and/or microphallus. Dysmorphic features have been reported in some patients but no consistent pattern has been noted.	Is a	False	Obesity (disorder)	Inferred relationship	Some
Skin striae due to obesity	Due to	True	Obesity (disorder)	Inferred relationship	Some	2
A rare genetic neurological disorder characterized by the association of congenital spastic paraplegia with global developmental delay and intellectual disability, ophthalmologic abnormalities (including nystagmus, reduced visual acuity, or hypermetropia), and obesity. Additional manifestations are brachy plagiocephaly and dysmorphic facial features. Brain imaging may show dilated ventricles, abnormal myelination, and mild generalized atrophy. Homozygous loss-of-function variants of KIDINS220 associated with a fetal lethal phenotype with ventriculomegaly and limb contractures have been reported.	Is a	False	Obesity (disorder)	Inferred relationship	Some
A rare genetic multiple congenital anomalies/dysmorphic syndrome characterized by intellectual disability, obesity, macrocephaly, behavioral abnormalities (such as aggressive tantrums and autistic-like behavior), and delayed speech development. Dysmorphic facial features include large, square forehead, prominent supraorbital ridges, broad nasal tip, large ears, prominent lower lip, and minor dental anomalies such as small upper lateral incisors and central incisor gap.	Is a	False	Obesity (disorder)	Inferred relationship	Some
A rare neurodevelopmental syndrome characterised by developmental delay, intellectual disability of varying severity and weight disorders (overweight/obesity and eating behaviour disorders including hyperphagia, tachyphagia, food impulsiveness and a feeling of permanent hunger). Additional clinical features include learning difficulties (may be combined with dysphasia, dyspraxia, dyscalculia, dysgraphia), severe language delay, behavioural disorders (stereotypies, impulsiveness or intolerance to frustration, self or hetero aggression, autism spectrum disorder) and non-specific dysmorphism. Epilepsy and ophthalmologic abnormalities can also be observed. Endocrine abnormalities are rarely associated.	Is a	False	Obesity (disorder)	Inferred relationship	Some
A rare overgrowth/obesity syndrome characterized by mild developmental delay (notably speech delay), behavior abnormalities (including autistic or attention deficit hyperactivity disorder features, hypersociability/overfriendliness), overweight/obesity and mild dysmorphic features (including deep set eyes, broad bulbous nasal tip, large, everted ears, and thin upper lip). Other clinical features include variable and mild intellectual disability when present, broad short hands, and feet.	Is a	False	Obesity (disorder)	Inferred relationship	Some
Obesity due to genetic disease.	Is a	True	Obesity (disorder)	Inferred relationship	Some

This concept is not in any reference sets

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Id	Description	Lang	Type	Status	Case?	Module
2531533010	Obesity (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
2535065012	Obesity	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
2537811012	Adiposis	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
2537812017	Adiposity	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
363081000195115	obesità	it	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
3971000077117	obésité	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
11441001000111	Adipositas	de	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
164781000274111	Fettleibigkeit	de	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
578391000274116	Obesität	de	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
578401000274118	Obesitas	de	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module