Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Scenic visual hallucinations |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Dissociative visual hallucinations |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Formed hallucinations of people |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Formed hallucinations of animals |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Formed hallucinations of insects |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Formed hallucinations of objects |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Sexual dysfunction caused by drug (finding) |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Abnormal adrenocorticotropic hormone |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Ectopic ACTH secretion |
Has interpretation |
False |
Abnormal |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Paraneoplastic ectopic secretion of ACTH |
Has interpretation |
False |
Abnormal |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Esophageal dysmotility following bariatric surgery (disorder) |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Ear examination abnormal |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Acquired prekallikrein deficiency |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Hereditary congenital prekallikrein deficiency (disorder) |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Congenital instability of bilateral hip joints (disorder) |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Instability of spinal joint due to and following traumatic injury (disorder) |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Achalasia due to Chagas disease (disorder) |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
Post-traumatic mutism |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
6 |
Acquired dysphasia (disorder) |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Traumatic rupture of posterior cruciate ligament of left knee joint (disorder) |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Right knee joint posterior cruciate ligament traumatic rupture |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Spastic paraplegia, intellectual disability, palmoplantar hyperkeratosis syndrome (disorder) |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
6 |
Extrinsic staining of teeth caused by drug (disorder) |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Posteruptive teeth staining (disorder) |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Teeth staining caused by metal (disorder) |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Teeth staining due to pulpal bleeding |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Teeth staining due to drugs (disorder) |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Intrinsic staining of tooth caused by tetracycline |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Posteruptive tooth staining caused by tetracycline |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Abnormal nervous system function |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Foreign accent syndrome (disorder) |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Ectopic renin secretion |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Tobacco deposit on teeth (disorder) |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
DIAPH1-related sensorineural hearing loss-thrombocytopenia syndrome |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Macrothrombocytopenia, lymphedema, developmental delay, facial dysmorphism, camptodactyly syndrome (disorder) |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Hereditary thrombocytopenia with early-onset myelofibrosis |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Betel deposit on teeth |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Cytosolic phospholipase-A2 alpha deficiency associated bleeding disorder (disorder) |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Antepartum hemorrhage with afibrinogenemia |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Hyperfibrinolysis |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Antepartum hemorrhage with coagulation defect (disorder) |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Antepartum haemorrhage with hyperfibrinolysis |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Antepartum hemorrhage with coagulation defect - delivered |
Has interpretation |
False |
Abnormal |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Antepartum hemorrhage with coagulation defect - not delivered |
Has interpretation |
False |
Abnormal |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Antepartum hemorrhage with hypofibrinogenemia |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Antepartum hemorrhage with disseminated intravascular coagulation (disorder) |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Density outside reference range |
Has interpretation |
False |
Abnormal |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Erythrokeratodermia cardiomyopathy syndrome |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
Maternal perinatal purpura (disorder) |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Fetal purpura (disorder) |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Chromodomain helicase dna-binding protein 3- related developmental delay, speech delay, intellectual disability, abnormalities of vision, facial dysmorphism syndrome (disorder) |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Perinatal disorder of skin and temperature regulation (disorder) |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
ARIA - amyloid-related imaging abnormality |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
ARIA-E - amyloid-related image abnormality of edema or effusion |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
ARIA-H - amyloid-related image abnormality of microhemorrhage or hemosiderosis |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Abnormal heart to thorax ratio of fetus (finding) |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Sexual dysfunction caused by amfetamine (finding) |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Autosomal dominant thrombocytopenia with platelet secretion defect |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Opioid-induced sexual dysfunction |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Severe autosomal recessive macrothrombocytopenia (disorder) |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Thrombocytopenia, anasarca, fever, renal insufficiency, organomegaly syndrome (disorder) |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Acquired antithrombin III deficiency |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Osteogenesis imperfecta type IIC (disorder) |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Congenital ichthyosis, microcephalus, tetraplegia syndrome (disorder) |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Premature separation of placenta with coagulation defect |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
A rare genetic coagulation disorder characterized by marked bleeding tendency and posttraumatic bleeding with easy bruising, soft tissue and muscle bleeding, hemarthroses, and menorrhagia due to an increase of soluble thrombomodulin in plasma with subsequent protein C activation and reduction of thrombin generation within a potential thrombus. Abnormal laboratory findings include markedly elevated plasma thrombomodulin, reduced prothrombin consumption, and decreased thrombin generation. |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Dysmotility of small intestine caused by drug |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Dysmotility of small intestine due to systemic disease (disorder) |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Discoloration of kidney (disorder) |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Perceptual disturbances co-occurrent and due to hypnotic withdrawal (disorder) |
Has interpretation |
False |
Abnormal |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Perceptual disturbances and seizures co-occurrent and due to hypnotic withdrawal (disorder) |
Has interpretation |
False |
Abnormal |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Brugada electrocardiograph pattern (finding) |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Congenital autosomal recessive small-platelet thrombocytopenia (disorder) |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Multifocal lymphangioendotheliomatosis, thrombocytopenia syndrome |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Spontaneous Brugada electrocardiograph pattern (finding) |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
A rare autosomal ichthyosis syndrome with prominent neurologic signs characterized by the association of congenital ichthyosis with global developmental delay, intellectual disability, infantile-onset seizures, and spastic tetraplegia. Brain imaging may show delayed myelination and cerebral atrophy. Marked intrafamilial variability has been reported. |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Ultrasonography of lung abnormal (finding) |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Pale face |
Has interpretation |
False |
Abnormal |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Discoloration of liver |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Provoked Brugada electrocardiograph pattern |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Behavioral disturbance due to multi-infarct dementia |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
Instability of joint of bilateral wrist regions (finding) |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Instability of joint of bilateral hands (finding) |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Instability of joint of bilateral elbows (finding) |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Instability of joint of sacrococcygeal region (finding) |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Abnormal rapid eye movement sleep (finding) |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Selective immunoglobulin dysfunction |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Hyperimmunoglobulin D with periodic fever |
Has interpretation |
False |
Abnormal |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Acquired protein S deficiency |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Acquired protein C deficiency |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Acquired heparin cofactor II deficiency (disorder) |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Abnormal fetal heart beat first noted during labor AND/OR delivery in liveborn infant |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Intrapartum hemorrhage with coagulation defect |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Parturient hemorrhage associated with hypofibrinogenemia |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Regular wide QRS complex tachycardia (disorder) |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Abnormal amniotic fluid |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Disorder of amniotic fluid turnover (disorder) |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Purulent amniotic fluid (finding) |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Pigmented purpuric dermatosis (disorder) |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
5 |
Lichen aureus |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
6 |
Progressive pigmentary dermatosis of Schamberg |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
6 |