| Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
| Melorheostosis of spine (disorder) |
Has interpretation |
True |
Above reference range (qualifier value) |
Inferred relationship |
Some |
3 |
| Melorheostosis of right foot (disorder) |
Has interpretation |
True |
Above reference range (qualifier value) |
Inferred relationship |
Some |
3 |
| Melorheostosis of left foot (disorder) |
Has interpretation |
True |
Above reference range (qualifier value) |
Inferred relationship |
Some |
3 |
| Melorheostosis of right lower leg (disorder) |
Has interpretation |
True |
Above reference range (qualifier value) |
Inferred relationship |
Some |
3 |
| Melorheostosis of left lower leg |
Has interpretation |
True |
Above reference range (qualifier value) |
Inferred relationship |
Some |
3 |
| Brazilian purpuric fever |
Has interpretation |
True |
Above reference range (qualifier value) |
Inferred relationship |
Some |
5 |
| A rare genetic multiple congenital anomalies/dysmorphic syndrome characterized by agenesis of the corpus callosum, borderline or mild intellectual disability, macrocephaly, and dysmorphic facial features (broad forehead, widely spaced eyes). Chiari type I malformation has also been reported in association. |
Has interpretation |
True |
Above reference range (qualifier value) |
Inferred relationship |
Some |
6 |
| A rare congenital disorder of glycosylation characterized by chronic, non-progressive liver disease, manifesting as mild steatosis with elevated serum transaminases and alkaline phosphatase, hypercholesterolemia, and decreased coagulation factors and ceruloplasmin. Transferrin glycosylation pattern is consistent with a type 2 congenital disorder of glycosylation. Liver biopsy may show mild non-progressive fibrosis. Patients usually remain asymptomatic, although delayed psychomotor development and hypotonia have been reported in single cases. |
Has interpretation |
True |
Above reference range (qualifier value) |
Inferred relationship |
Some |
1 |
| A rare functioning neuroendocrine tumour of pancreas characterised by a typically well-differentiated neoplasm composed of cells expressing serotonin. Patients may present with atypical carcinoid syndrome with abdominal pain, diarrhoea, weight loss, and/or flushing. Carcinoid syndrome is usually present only when there are liver metastases. The tumours tend to be larger than non-functioning tumours and are associated with a poorer prognosis because they are almost always metastatic. |
Has interpretation |
True |
Above reference range (qualifier value) |
Inferred relationship |
Some |
2 |
| 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. |
Has interpretation |
True |
Above reference range (qualifier value) |
Inferred relationship |
Some |
2 |
| Puerperal pyrexia |
Has interpretation |
True |
Above reference range (qualifier value) |
Inferred relationship |
Some |
2 |
| Puerperal pyrexia of unknown origin |
Has interpretation |
True |
Above reference range (qualifier value) |
Inferred relationship |
Some |
2 |
| puerperal pyreksi af ukendt oprindelse, barn født med postnatal komplikation |
Has interpretation |
False |
Above reference range (qualifier value) |
Inferred relationship |
Some |
2 |
| Puerperal pyreksi af ukendt oprindelse med postnatal komplikation |
Has interpretation |
False |
Above reference range (qualifier value) |
Inferred relationship |
Some |
2 |
| Fibrinolysis - postpartum |
Has interpretation |
True |
Above reference range (qualifier value) |
Inferred relationship |
Some |
2 |
| A rare primary bone dysplasia with increased bone density characterized by slowly progressive endosteal hyperostosis and osteosclerosis exclusively of the skull base and the calvaria, resulting in entrapment and dysfunction of cranial nerves I, II, V, VII, and VIII. First symptoms often appear during the second decade of life and include disturbances in smell, vision, facial sensation and expression, hearing, and balance, as well as headaches due to increased ocular and intracranial pressure. After the fourth decade, radiological progression is minimal, although decreased intracranial volume can lead to death in severe cases. |
Has interpretation |
True |
Above reference range (qualifier value) |
Inferred relationship |
Some |
4 |
| Urine substance level above reference range (finding) |
Has interpretation |
True |
Above reference range (qualifier value) |
Inferred relationship |
Some |
1 |
| Blood substance level above reference range |
Has interpretation |
True |
Above reference range (qualifier value) |
Inferred relationship |
Some |
1 |
| Increased estrogen level |
Has interpretation |
True |
Above reference range (qualifier value) |
Inferred relationship |
Some |
1 |
| Parturient hemorrhage associated with hyperfibrinolysis |
Has interpretation |
True |
Above reference range (qualifier value) |
Inferred relationship |
Some |
3 |
| A rare disorder of ornithine metabolism characterized by global developmental delay, alopecia, macrocephaly, and dysmorphic facial features (including high and broad forehead, hypertelorism, ptosis, blepharophimosis, downslanting palpebral fissures, deep-set eyes, large ears, and retrognathia or high arched palate). Additional reported manifestations are sensorineural hearing loss, spasticity, hypotonia, hypoplastic nails, cryptorchidism, and clinodactyly, among others. Brain imaging may show white matter abnormalities, periventricular cysts, enlarged lateral ventricles, or prominent perivascular spaces. |
Has interpretation |
True |
Above reference range (qualifier value) |
Inferred relationship |
Some |
3 |
| A rare genetic neurological disorder characterized by pediatric onset of calcifying leukoencephalopathy and skeletal dysplasia. Reported structural brain abnormalities include agenesis of corpus callosum, ventriculomegaly, congenital hydrocephalus, pontocerebellar hypoplasia, periventricular calcifications, Dandy-Walker malformation and absence of microglia. Characteristic skeletal features include increased bone mineral density (reported in skull, pelvic bone and vertebrae), platyspondyly, and under-modeling of tubular bones with widened/radiolucent metaphysis and constricted/sclerotic diaphysis. |
Has interpretation |
True |
Above reference range (qualifier value) |
Inferred relationship |
Some |
3 |
| Amniotic fluid volume above reference range (finding) |
Has interpretation |
True |
Above reference range (qualifier value) |
Inferred relationship |
Some |
1 |
| 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. |
Has interpretation |
True |
Above reference range (qualifier value) |
Inferred relationship |
Some |
4 |
| A rare Prader-Willi-like syndrome characterized by arthrogryposis, including contractures of the proximal and distal interphalangeal joints, and autism spectrum disorder due to MAGEL2 mutation. Overlapping phenotypes with Prader-Willi syndrome include hypotonia, feeding difficulties, weight gain, developmental delay, intellectual disability and hypogonadism. Minority of patients manifest hyperphagia and morbid obesity in contrast to patients with Prader-Willi syndrome. |
Has interpretation |
True |
Above reference range (qualifier value) |
Inferred relationship |
Some |
4 |
| Fluid thrill of amniotic fluid present |
Has interpretation |
True |
Above reference range (qualifier value) |
Inferred relationship |
Some |
2 |
| Postpartum fibrinolysis with hemorrhage |
Has interpretation |
True |
Above reference range (qualifier value) |
Inferred relationship |
Some |
3 |
| A rare primary bone dysplasia characterized by multiple, small, round to ovoid osteosclerotic foci with a predilection for the epiphyses and metaphyses of long tubular bones as well as the pelvis, scapula, carpal, and tarsal bones. The condition is usually clinically silent and discovered only incidentally, although some patients may experience mild articular pain with or without joint effusion. Bone strength is normal. |
Has interpretation |
True |
Above reference range (qualifier value) |
Inferred relationship |
Some |
2 |
| A rare genetic autoinflammatory syndrome characterized by early-onset of repeated episodes of fever, nodular neutrophil-rich panniculitis, arthralgia, and lipodystrophy. Additional reported features include diarrhea, failure to thrive, lymphadenopathy, and vasculitis. Laboratory examination may reveal elevated serum C-reactive protein and leukocytosis with neutrophilia in the absence of infection. |
Has interpretation |
True |
Above reference range (qualifier value) |
Inferred relationship |
Some |
2 |
| Placental volume above reference range (finding) |
Has interpretation |
True |
Above reference range (qualifier value) |
Inferred relationship |
Some |
2 |
| Hypercalcemia caused by thiazide and/or retinol (disorder) |
Has interpretation |
True |
Above reference range (qualifier value) |
Inferred relationship |
Some |
1 |
| A rare disease with malignant hyperthermia characterized by exercise-induced life-threatening hyperthermia with a body temperature over 40°C and signs of encephalopathy ranging from confusion to convulsions or coma. Incidence increases with rising ambient temperature and relative humidity. Manifestations may include rhabdomyolysis (presenting with myalgia, muscle weakness, and myoglobinuria), tachycardia, and in severe cases multiorgan failure. |
Has interpretation |
True |
Above reference range (qualifier value) |
Inferred relationship |
Some |
1 |
| A rare haematologic disease characterised by high serum viscosity due to polyclonal expansion of immunoglobulins, most commonly in the context of Waldenström's macroglobulinaemia, as well as a variety of disorders of immune dysregulation. Patients present with signs and symptoms involving multiple organs, such as bleeding diathesis, mucosal bleeding, retinal haemorrhage, headache, stroke, pulmonary hypertension, and congestive heart failure. |
Has interpretation |
True |
Above reference range (qualifier value) |
Inferred relationship |
Some |
1 |
| Classical type acute febrile neutrophilic dermatosis |
Has interpretation |
True |
Above reference range (qualifier value) |
Inferred relationship |
Some |
2 |
| Classical type acute febrile neutrophilic dermatosis |
Has interpretation |
True |
Above reference range (qualifier value) |
Inferred relationship |
Some |
3 |
| Acute febrile neutrophilic dermatosis due to neoplastic disease |
Has interpretation |
True |
Above reference range (qualifier value) |
Inferred relationship |
Some |
4 |
| Acute febrile neutrophilic dermatosis due to neoplastic disease |
Has interpretation |
True |
Above reference range (qualifier value) |
Inferred relationship |
Some |
5 |
| Hypermobility syndrome |
Has interpretation |
True |
Above reference range (qualifier value) |
Inferred relationship |
Some |
3 |
| Hypermobile Ehlers-Danlos syndrome (disorder) |
Has interpretation |
True |
Above reference range (qualifier value) |
Inferred relationship |
Some |
5 |
| Generalized benign joint hypermobility |
Has interpretation |
True |
Above reference range (qualifier value) |
Inferred relationship |
Some |
3 |
| Localized benign joint hypermobility |
Has interpretation |
True |
Above reference range (qualifier value) |
Inferred relationship |
Some |
3 |
| Gamma-enolase level above reference range (finding) |
Has interpretation |
True |
Above reference range (qualifier value) |
Inferred relationship |
Some |
1 |
| A rare, syndromic intellectual disability characterized by hypotonia, global developmental delay, limited or absent speech, intellectual disability, macrocephaly, mild dysmorphic features, seizures and autism spectrum disorder. Associated ophthalmologic, heart, skeletal and central nervous system anomalies have been reported. |
Has interpretation |
True |
Above reference range (qualifier value) |
Inferred relationship |
Some |
7 |
| Keratin, type I cytoskeletal 19 fragment above reference range (finding) |
Has interpretation |
True |
Above reference range (qualifier value) |
Inferred relationship |
Some |
1 |
| A rare systemic disease characterized by generalized joint hypermobility with recurrent joint dislocations, redundant and hyperextensible skin with poor wound healing and abnormal scarring, easy bruising, and osteopenia/osteoporosis. Additional manifestations include hypotonia, delayed motor development, foot deformities, prominent superficial veins in the chest region, vascular complications (like mitral valve prolapse and aortic root dilation), hernias, dental anomalies, scoliosis, and facial dysmorphisms (like high palate, micrognathia, narrow palate). Mode of inheritance is autosomal recessive. |
Has interpretation |
True |
Above reference range (qualifier value) |
Inferred relationship |
Some |
6 |
| A rare otorhinolaryngologic disease characterized by an indolent submucosal mass of variable size and extent, most commonly arising in the anterior nasal cavity, involving the nasal septum and lateral nasal wall, and potentially extending into the adjacent sinuses. Occurrence in the larynx and lower respiratory tract or the orbit is rare. Histological examination shows concentric angiocentric stromal fibrosis (onionskin fibrosis) and prominent eosinophils. Increased numbers of IgG4-positive plasma cells in the lesion may also be observed, in addition to elevated serum IgG4. Patients typically present with long-standing obstructive symptoms. |
Has interpretation |
True |
Above reference range (qualifier value) |
Inferred relationship |
Some |
2 |
| 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. |
Has interpretation |
True |
Above reference range (qualifier value) |
Inferred relationship |
Some |
6 |
| Hidradenitis suppurativa pyoderma gangrenosum complex (disorder) |
Has interpretation |
False |
Above reference range (qualifier value) |
Inferred relationship |
Some |
3 |
| Acute febrile neutrophilic dermatosis of hand (disorder) |
Has interpretation |
True |
Above reference range (qualifier value) |
Inferred relationship |
Some |
2 |
| Acute febrile neutrophilic dermatosis of hand (disorder) |
Has interpretation |
True |
Above reference range (qualifier value) |
Inferred relationship |
Some |
3 |
| Hypoxic nephrosis (disorder) |
Has interpretation |
True |
Above reference range (qualifier value) |
Inferred relationship |
Some |
2 |
| Pustular pyoderma gangrenosum (disorder) |
Has interpretation |
False |
Above reference range (qualifier value) |
Inferred relationship |
Some |
3 |
| Pyoderma gangrenosum due to inflammatory polyarthropathy (disorder) |
Has interpretation |
False |
Above reference range (qualifier value) |
Inferred relationship |
Some |
4 |
| Pyoderma gangrenosum due to inflammatory bowel disease (disorder) |
Has interpretation |
False |
Above reference range (qualifier value) |
Inferred relationship |
Some |
4 |
| Ulcerative pyoderma gangrenosum |
Has interpretation |
False |
Above reference range (qualifier value) |
Inferred relationship |
Some |
4 |
| Pyoderma gangrenosum due to hematological disorder |
Has interpretation |
False |
Above reference range (qualifier value) |
Inferred relationship |
Some |
4 |
| Superficial vegetating pyoderma gangrenosum (disorder) |
Has interpretation |
False |
Above reference range (qualifier value) |
Inferred relationship |
Some |
4 |
| Castleman disease with immunoglobulin M monoclonal gammopathy of uncertain significance (disorder) |
Has interpretation |
True |
Above reference range (qualifier value) |
Inferred relationship |
Some |
2 |
| Castleman disease with immunoglobulin M monoclonal gammopathy of uncertain significance (disorder) |
Has interpretation |
True |
Above reference range (qualifier value) |
Inferred relationship |
Some |
3 |
| Microproteinuria |
Has interpretation |
True |
Above reference range (qualifier value) |
Inferred relationship |
Some |
1 |
| Grade A2 albuminuria |
Has interpretation |
True |
Above reference range (qualifier value) |
Inferred relationship |
Some |
1 |
| Grade A3 albuminuria |
Has interpretation |
True |
Above reference range (qualifier value) |
Inferred relationship |
Some |
1 |
| 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. |
Has interpretation |
True |
Above reference range (qualifier value) |
Inferred relationship |
Some |
4 |
| A rare genetic disease characterized by early-onset severe obesity due to mutations in single genes acting on the development and function of the hypothalamus or the leptin-melanocortin pathway, leading to disruption of energy homeostasis and endocrine dysfunction. Patients present with a body mass index over three standard deviations above normal at less than five years of age, accompanied by a variety of signs and symptoms according to the mutated gene, including hyperphagia, insulin resistance, reduced basal metabolic rate, or hypogonadism, among others. |
Has interpretation |
True |
Above reference range (qualifier value) |
Inferred relationship |
Some |
1 |
| A form of monogenic obesity with characteristics of severe early-onset obesity and marked hyperphagia. Patients with congenital leptin deficiency are severely hyperphagic from early infancy and, although birthweight is normal, they rapidly become obese during early childhood. An increased susceptibility to infections has also been reported in these infants and appears to be associated with reduced numbers of circulating CD4+ T cells, and impaired T cell proliferation and cytokine release. Absence of serum leptin is caused by homozygous frameshift or missense mutations in the ob gene (7q31.3) and is inherited as an autosomal recessive trait. |
Has interpretation |
True |
Above reference range (qualifier value) |
Inferred relationship |
Some |
3 |
| A rare genetic multiple congenital anomalies/dysmorphic syndrome characterized by overgrowth and macrocephaly with megalencephaly apparent at birth, global developmental delay, intellectual disability, and dysmorphic facial features (including frontal bossing, long face, sparse eyebrows, hypertelorism, downslanting palpebral fissures, and prognathism). Patients may exhibit tall stature with dolichostenomelia, arachnodactyly, kyphoscoliosis, and joint laxity, as well as neurologic manifestations, such as hypotonia, gait ataxia, or seizures. Brain imaging may show increased white matter volume, thick corpus callosum, or small cerebellum. |
Has interpretation |
True |
Above reference range (qualifier value) |
Inferred relationship |
Some |
5 |
| A rare, idiopathic nephrotic syndrome characterized by the triad of proteinuria, hypoalbuminemia and edema in patients who do not respond, or only partially respond, to the initial trial of corticosteroids. Patients may be multidrug resistant or may be sensitive to second-line immunosuppressive therapy. |
Has interpretation |
True |
Above reference range (qualifier value) |
Inferred relationship |
Some |
2 |
| A rare, idiopathic nephrotic syndrome characterized by pediatric onset of proteinuria, hypoalbuminemia and edema. Patients respond successfully to the initial standard course of corticosteroids but are resistant to standard therapy for a subsequent relapse and following this relapse remain steroid-resistant. |
Has interpretation |
True |
Above reference range (qualifier value) |
Inferred relationship |
Some |
4 |
| A rare hematologic disease characterized by symptoms of mast cell activation in the absence of cutaneous findings, as well as absence of diagnostic criteria of systemic mastocytosis with tryptase levels of less than 20 ng/ml and normal to low burden of mast cells. Bone marrow biopsy reveals the presence of monoclonal mast cells carrying the KIT D816V mutation and/or expressing CD25. Patients present with recurrent episodes of flushing, headache, hypotension, abdominal cramping, nausea, diarrhea, cardiac arrhythmias, bronchoconstriction, and bleeding diathesis, among others. |
Has interpretation |
False |
Above reference range (qualifier value) |
Inferred relationship |
Some |
1 |
| A rare hematologic disease characterized by symptoms of mast cell activation in the absence of cutaneous findings, as well as absence of diagnostic criteria of systemic mastocytosis with tryptase levels of less than 20 ng/ml and normal to low burden of mast cells. Bone marrow biopsy reveals the presence of monoclonal mast cells carrying the KIT D816V mutation and/or expressing CD25. Patients present with recurrent episodes of flushing, headache, hypotension, abdominal cramping, nausea, diarrhea, cardiac arrhythmias, bronchoconstriction, and bleeding diathesis, among others. |
Has interpretation |
False |
Above reference range (qualifier value) |
Inferred relationship |
Some |
2 |
| Hepatitis C antibody detected with elevated alanine transaminase (finding) |
Has interpretation |
True |
Above reference range (qualifier value) |
Inferred relationship |
Some |
2 |
| Uraemia following molar pregnancy |
Has interpretation |
True |
Above reference range (qualifier value) |
Inferred relationship |
Some |
1 |
| Uraemia following ectopic pregnancy |
Has interpretation |
True |
Above reference range (qualifier value) |
Inferred relationship |
Some |
1 |
| A rare hereditary periodic fever syndrome characterized by infantile or childhood onset of episodes of fever and cold-induced urticaria-like rash and arthralgias. Ocular features such as conjunctivitis and uveitis may also be present. Presentation is typically mild, and symptoms resolve without treatment in most cases. |
Has interpretation |
True |
Above reference range (qualifier value) |
Inferred relationship |
Some |
2 |
| Lipoprotein (a) hyperlipoproteinemia (disorder) |
Has interpretation |
True |
Above reference range (qualifier value) |
Inferred relationship |
Some |
1 |
| Albuminuria |
Has interpretation |
True |
Above reference range (qualifier value) |
Inferred relationship |
Some |
1 |
| Methemalbuminuria |
Has interpretation |
True |
Above reference range (qualifier value) |
Inferred relationship |
Some |
1 |
| Orthostatic proteinuria |
Has interpretation |
True |
Above reference range (qualifier value) |
Inferred relationship |
Some |
2 |
| Mixed proteinuria |
Has interpretation |
True |
Above reference range (qualifier value) |
Inferred relationship |
Some |
1 |
| Persistent orthostatic proteinuria (finding) |
Has interpretation |
True |
Above reference range (qualifier value) |
Inferred relationship |
Some |
2 |
| Proteinuria |
Has interpretation |
True |
Above reference range (qualifier value) |
Inferred relationship |
Some |
1 |
| Persistent microalbuminuria due to type 2 diabetes mellitus (disorder) |
Has interpretation |
True |
Above reference range (qualifier value) |
Inferred relationship |
Some |
1 |
| Persistent microalbuminuria due to type 1 diabetes mellitus (disorder) |
Has interpretation |
True |
Above reference range (qualifier value) |
Inferred relationship |
Some |
1 |
| Gestational proteinuria without hypertension (disorder) |
Has interpretation |
True |
Above reference range (qualifier value) |
Inferred relationship |
Some |
1 |
| Microalbuminuria due to type 1 diabetes mellitus |
Has interpretation |
True |
Above reference range (qualifier value) |
Inferred relationship |
Some |
3 |
| Microalbuminuria due to type 2 diabetes mellitus (disorder) |
Has interpretation |
True |
Above reference range (qualifier value) |
Inferred relationship |
Some |
3 |
| Microalbuminuric diabetic nephropathy |
Has interpretation |
True |
Above reference range (qualifier value) |
Inferred relationship |
Some |
3 |
| Asymptomatic proteinuria |
Has interpretation |
True |
Above reference range (qualifier value) |
Inferred relationship |
Some |
2 |
| Persistent gestational proteinuria (disorder) |
Has interpretation |
True |
Above reference range (qualifier value) |
Inferred relationship |
Some |
2 |
| Intermittent orthostatic proteinuria |
Has interpretation |
True |
Above reference range (qualifier value) |
Inferred relationship |
Some |
1 |
| Intermittent gestational proteinuria |
Has interpretation |
True |
Above reference range (qualifier value) |
Inferred relationship |
Some |
2 |
| Gestational edema with proteinuria |
Has interpretation |
True |
Above reference range (qualifier value) |
Inferred relationship |
Some |
2 |
| Pregnancy-induced edema and proteinuria without hypertension |
Has interpretation |
True |
Above reference range (qualifier value) |
Inferred relationship |
Some |
2 |
| Gestational proteinuria |
Has interpretation |
True |
Above reference range (qualifier value) |
Inferred relationship |
Some |
1 |
| Persistent Bence Jones proteinuria (finding) |
Has interpretation |
True |
Above reference range (qualifier value) |
Inferred relationship |
Some |
2 |
| Bence-Jones proteinuria (finding) |
Has interpretation |
True |
Above reference range (qualifier value) |
Inferred relationship |
Some |
1 |
| Relapsing fever caused by Borrelia miyamotoi |
Has interpretation |
True |
Above reference range (qualifier value) |
Inferred relationship |
Some |
3 |
| Relapsing fever caused by Borrelia latyschewii (disorder) |
Has interpretation |
True |
Above reference range (qualifier value) |
Inferred relationship |
Some |
2 |
| Relapsing fever caused by Borrelia hermsii |
Has interpretation |
True |
Above reference range (qualifier value) |
Inferred relationship |
Some |
2 |
| Relapsing fever caused by Borrelia venezuelensis |
Has interpretation |
True |
Above reference range (qualifier value) |
Inferred relationship |
Some |
2 |
| Relapsing fever caused by Borrelia mazzottii (disorder) |
Has interpretation |
True |
Above reference range (qualifier value) |
Inferred relationship |
Some |
2 |
FHIR