Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Familial obesity |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Constitutional obesity |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Hyperplastic-hypertrophic obesity |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Lifelong obesity (disorder) |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Buffalo obesity |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Hypertrophy of fat pad of knee |
Has interpretation |
False |
Above reference range |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Adult-onset obesity |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
On examination - overweight |
Has interpretation |
False |
Above reference range |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Body mass index (kg/m²) equal to or greater than 40. |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
On examination - obese |
Has interpretation |
False |
Above reference range |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Drug-induced obesity (disorder) |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Hyperplastic obesity |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Obese |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Obesity |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Obesity by adipocyte growth pattern (disorder) |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
obésité selon l'âge d'apparition |
Has interpretation |
False |
Above reference range |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Obesity by contributing factors (disorder) |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Obesity by fat distribution pattern (disorder) |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Simple obesity |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Choroideremia with deafness and obesity syndrome |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Syndromic X-linked intellectual disability type 7 (disorder) |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Wilson-Turner syndrome (WTS) is a very rare X-linked multisystem genetic disease characterized by intellectual disability, truncal obesity, gynecomastia, hypogonadism, dysmorphic facial features, and short stature. |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Hydrocephalus with obesity and hypogonadism syndrome |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
MEHMO syndrome |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Obesity-colitis-hypothyroidism-cardiac hypertrophy-developmental delay syndrome is characterised 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 interpretation |
True |
Above reference range |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
5 |
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. |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Overweight in adulthood with body mass index of 25 or more but less than 30 (finding) |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Obesity caused by energy imbalance (disorder) |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Macrocephaly, obesity, mental disability, ocular abnormality syndrome (disorder) |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
MORM syndrome |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Obesity due to melanocortin 4 receptor deficiency (disorder) |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Severe obesity complicating pregnancy |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Childhood obesity (disorder) |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Severe obesity |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Colobomatous microphthalmia, obesity, hypogenitalism, intellectual disability syndrome |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
Obesity due to CEP19 deficiency |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Severe early-onset obesity insulin resistance syndrome due to SH2B adaptor protein 1 deficiency (disorder) |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
A rare genetic form of obesity with characteristics of severe early-onset obesity, hyperphagia and variable presence of cognitive impairment and behavioural disorder, including autistic spectrum behaviour, impaired concentration and memory deficit. Some patients present with Prader-Willi-like features such as hypotonia, developmental delay, intellectual disability, short stature, hypopituitarism and dysmorphic facial features. |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
A rare genetic non-syndromic obesity disease with characteristics of severe early-onset obesity associated with major hyperphagia and endocrine abnormalities resulting from leptin receptor deficiency. Caused by homozygous mutation in the gene encoding the leptin receptor (LEPR) on chromosome 1p31. |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Overweight in childhood |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Maternal obesity complicating pregnancy, childbirth and the puerperium, antepartum |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Proopiomelanocortin deficiency syndrome |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Obesity in mother complicating childbirth (disorder) |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Prader-Willi-like syndrome |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
Intellectual disability, seizures, macrocephaly, obesity syndrome (disorder) |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
Intellectual disability, obesity, brain malformation, facial dysmorphism syndrome |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Rapid-onset childhood obesity, hypothalamic dysfunction, hypoventilation, autonomic dysregulation syndrome (disorder) |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Intellectual disability, obesity, prognathism, eye and skin anomalies syndrome (disorder) |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
Body mass index (kg/m²) from 30.00 to 34.99. |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Body mass index (kg/m²) from 35.00 to 39.99. |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Obese class III |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Hypertrophy of fat pad of right knee (disorder) |
Has interpretation |
False |
Above reference range |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Hypertrophy of fat pad of left knee |
Has interpretation |
False |
Above reference range |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Obesity in adolescence (disorder) |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Subcorneal pustular dermatosis with paraproteinemia (disorder) |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Subcorneal pustular dermatosis with paraproteinemia (disorder) |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
Down syndrome co-occurrent with leukemoid reaction associated transient neonatal pustulosis (disorder) |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
Episodic angioedema with eosinophilia (disorder) |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Liver function test above reference range (finding) |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Direct bilirubin above reference range |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Pulmonary arterial pressure increased (finding) |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Eosinophilia due to infectious disease (disorder) |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Fever caused by severe acute respiratory syndrome coronavirus 2 (disorder) |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Eosinophilic myositis (disorder) |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Fasciitis with eosinophilia syndrome |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Eosinophilic colitis |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Eosinophilic myopathy |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Eosinophilic fasciitis caused by L-tryptophan (disorder) |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Idiopathic eosinophilic myositis (disorder) |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Eosinophilic ulcerative colitis |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Carcinoid syndrome (disorder) |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Carcinoid crisis (disorder) |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Carcinoid syndrome diarrhoea |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Viral load increased |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Postmortem blood drug level increased |
Has interpretation |
False |
Above reference range |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Toxic goiter |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
goitre diffus toxique avec exophtalmie et avec crise aiguë thyrotoxique |
Has interpretation |
False |
Above reference range |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
Toxic uninodular goiter with thyrotoxic crisis |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Toxic diffuse goiter with thyrotoxic crisis |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Toxic diffuse goiter with pretibial myxedema |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Toxic multinodular goiter with thyrotoxic crisis |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Exophthalmos due to toxic diffuse goiter (disorder) |
Has interpretation |
False |
Above reference range |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
5 |
Toxic nodular goiter with thyrotoxic storm |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Graves' disease with acropachy AND with thyrotoxic crisis |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
Toxic diffuse goiter with acropachy |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Graves' disease with pretibial myxedema AND with thyrotoxic crisis |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
5 |
Toxic diffuse goiter with no crisis (disorder) |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Toxic diffuse goitre with crisis |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Toxic uninodular goitre with no crisis |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Toxic multinodular goiter with no crisis |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Thyrotoxicosis due to Graves' disease (disorder) |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Toxic diffuse goiter |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Graves' disease |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Neonatal Graves' disease |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Toxic nodular goiter |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Toxic multinodular goiter (disorder) |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Toxic uninodular goiter |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Graves' disease in remission |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
Juvenile Graves' disease |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Dyshormonogenic goiter |
Has interpretation |
False |
Above reference range |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Thyroglobulin synthesis defect (disorder) |
Has interpretation |
False |
Above reference range |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |