| Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
| Obesity by fat distribution pattern (disorder) |
Is a |
True |
Obesity (disorder) |
Inferred relationship |
Some |
|
| adipositas specificeret iht. alder ved debut |
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 |
|
| Overdreven vægtstigning under graviditet |
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 |
True |
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 |
True |
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 |
True |
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 |
True |
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 |
True |
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 |
True |
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 |
True |
Obesity (disorder) |
Inferred relationship |
Some |
|
| Alstrom syndrome |
Is a |
True |
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 characterized 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 heterogenous 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 |
True |
Obesity (disorder) |
Inferred relationship |
Some |
|
| A rare genetic syndromic intellectual disability disorder with characteristics of 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 |
True |
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 (disorder) |
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 |
True |
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 |
True |
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 |
True |
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 |
True |
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 |
True |
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 |
True |
Obesity (disorder) |
Inferred relationship |
Some |
|
FHIR