Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Afibrinogenemia following ectopic pregnancy (disorder) |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Some |
4 |
Defibrination syndrome following molar pregnancy |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Some |
1 |
Defibrination syndrome following ectopic pregnancy (disorder) |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Some |
1 |
Paroxysmal choreoathetosis |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Some |
1 |
Choreoathetosis |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Some |
2 |
Paroxysmal nonkinesigenic dyskinesia (disorder) |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Some |
3 |
Paroxysmal kinesigenic dyskinesia (disorder) |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Some |
3 |
Infantile Convulsions and paroxysmal ChoreoAthetosis (ICCA) syndrome is a neurological condition characterised by the occurrence of seizures during the first year of life and choreoathetotic dyskinetic attacks during childhood or adolescence. |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Some |
4 |
Paroxysmal dystonic choreoathetosis with episodic ataxia and spasticity (disorder) |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Some |
2 |
Acquired choreiform dyspraxia |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Some |
6 |
A rare multiple congenital anomalies/dysmorphic syndrome characterized by profound intellectual disability, choreoathetosis, progressive spastic diplegia, progressive tapetoretinal degeneration with loss of retinal vessels, and glomerulopathy resulting in death late in the first or early in the second decade of life. Absence of the cerebellar granular layer has been reported. There have been no further descriptions in the literature since 1982. |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Some |
8 |
Chorea due to Huntington disease-like 3 (disorder) |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Some |
4 |
Chorea due to Huntington disease-like 2 (disorder) |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Some |
3 |
Chorea due to Huntington disease-like 1 (disorder) |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Some |
4 |
Chorea co-occurrent and due to Wilson disease (disorder) |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Some |
7 |
Chorea gravidarum |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Some |
4 |
Chronic progressive non-hereditary chorea |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Some |
4 |
Westphal-Strumpell syndrome |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Some |
6 |
Choreic cerebral palsy |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Some |
1 |
A form of dyskinetic cerebral palsy with a combination of chorea and athetosis; movements are irregular, but twisting and curving. |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Some |
2 |
A rare severe neurodegenerative disorder that is considered one of the phenocopies of Huntington Disease (HD) affecting patients of African descent and characterized by a triad of movement (chorea, oculomotor, parkinsonism), psychiatric (prominently sadness, irritability and anxiety), and cognitive abnormalities (early cognitive decline and subcortical-like dementia). |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Some |
2 |
Hemichorea |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Some |
3 |
Post-hemiplegic chorea |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Some |
1 |
Hemichorea due to injury of head (disorder) |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Some |
4 |
Hemichorea due to cerebral arteriovenous malformation (disorder) |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Some |
4 |
Hemichorea due to abscess of brain (disorder) |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Some |
4 |
Hemichorea due to cerebral hemorrhage (disorder) |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Some |
4 |
Hemichorea due to neoplasm of brain (disorder) |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Some |
4 |
Hemichorea due to cerebral infarction (disorder) |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Some |
4 |
Hemichorea due to multiple sclerosis (disorder) |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Some |
1 |
Systemic exogenous pigmentation of oral mucosa |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Some |
2 |
Amalgam tattoo |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Some |
1 |
Exogenous pigmentation of oral mucosa |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Some |
2 |
Drug-induced oral pigmentation (disorder) |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Some |
2 |
Digital breast tomosynthesis abnormal |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Some |
1 |
Acute ST segment elevation myocardial infarction of atrium |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Some |
2 |
Fluency disorder due to and following embolic cerebrovascular accident (disorder) |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Some |
1 |
Acute ST segment elevation myocardial infarction due to occlusion of proximal portion of circumflex branch of left coronary artery (disorder) |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Some |
2 |
Acute ST segment elevation myocardial infarction due to distal left circumflex coronary artery occlusion |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Some |
2 |
Acute ST segment elevation myocardial infarction due to obtuse marginal branch of left circumflex coronary artery occlusion |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Some |
2 |
Acute ST segment elevation myocardial infarction due to posterolateral branch of left circumflex coronary artery occlusion |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Some |
2 |
Acute ST segment elevation myocardial infarction due to mid left circumflex coronary artery occlusion |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Some |
2 |
Chorea due to injury of head (disorder) |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Some |
1 |
Chorea following injury |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Some |
1 |
Postpartum hemolysis-elevated liver enzymes-low platelet count syndrome |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Some |
3 |
Fanconi anemia of complementation group C |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Some |
7 |
Mild hereditary factor VIII deficiency disease with high response inhibitor (disorder) |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Some |
1 |
Mild hereditary factor VIII deficiency disease with low response inhibitor |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Some |
1 |
Severe hereditary factor VIII deficiency disease with high response inhibitor (disorder) |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Some |
1 |
Severe hereditary factor VIII deficiency disease with low response inhibitor |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Some |
1 |
Moderate hereditary factor VIII deficiency disease with high response inhibitor |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Some |
1 |
Moderate hereditary factor VIII deficiency disease with low response inhibitor |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Some |
1 |
Severe hereditary factor IX deficiency disease with high response inhibitor |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Some |
1 |
Severe hereditary factor IX deficiency disease with low response inhibitor (disorder) |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Some |
1 |
Moderate hereditary factor IX deficiency disease with high response inhibitor |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Some |
1 |
Moderate hereditary factor IX deficiency disease with low response inhibitor (disorder) |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Some |
1 |
Mild hereditary factor IX deficiency disease with high response inhibitor |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Some |
1 |
Mild hereditary factor IX deficiency disease with low response inhibitor (disorder) |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Some |
1 |
Pancytopenia caused by colchicine (disorder) |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Some |
1 |
Pancytopenia caused by non-steroidal anti-inflammatory agent (disorder) |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Some |
1 |
Tooth eruption disorder (disorder) |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Some |
2 |
Altered passive eruption of teeth |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Some |
3 |
Failure of tooth eruption |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Some |
2 |
Overeruption of tooth |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Some |
2 |
Supereruption of unopposed tooth |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Some |
3 |
Supereruption of tooth associated with malocclusion |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Some |
3 |
Submerging tooth |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Some |
2 |
A tooth which erupts after birth in the neonatal period. |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Some |
2 |
Failure of tooth eruption associated with tooth impaction (disorder) |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Some |
2 |
Late tooth eruption |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Some |
2 |
An ectopic tooth that has erupted on the lingual aspect of the maxilla or mandible. |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Some |
2 |
Trichodermodysplasia-dental alterations syndrome is a rare, genetic ectodermal dysplasia syndrome characterized by sparse, thin, brittle scalp hair, as well as sparse eyebrows, eyelashes, axillary and pubic hair, delayed eruption of deciduous teeth and hypodontia of both dentitions. Mild palmoplantar keratosis, café-au-lait spots on back, mild dystrophy of nails, and tibial deflection of toes are also associated. There have been no further descriptions in the literature since 1986. |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Some |
6 |
Leukoencephalopathy, ataxia, hypodontia, hypomyelination syndrome (disorder) |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Some |
7 |
Premature tooth eruption |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Some |
2 |
Natal tooth |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Some |
2 |
Obstructed tooth eruption |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Some |
2 |
Labial ectopic tooth |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Some |
2 |
A rare malformation syndrome characterized by generalized multiple steatocystomas and natal teeth. |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Some |
3 |
A rare ectodermal dysplasia syndrome characterized by neonatal teeth, trichodystrophy (with straw-like, discolored and fragile hair), onychodystrophy, and malformation of the hands and feet consisting of simian-like hands with transverse palmar creases and prominent interdigital folds, brachydactyly, and marked shortness of the first metacarpal and metatarsal bones with hypoplasia of the distal phalanges. There have been no further descriptions in the literature since 1997. |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Some |
4 |
Noneruption of teeth - maxillary hypoplasia - genu valgum is an extremely rare syndrome that is characterized by multiple unerupted permanent teeth, hypoplasia of the alveolar process and of the maxillo-zygomatic region, severe genu valgum and deformed ears. |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Some |
5 |
Natal teeth (disorder) |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Some |
2 |
Delayed generalised tooth eruption due to systemic disease |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Some |
3 |
A rare genetic odontologic disease characterized by failure of eruption of non-ankylosed permanent teeth without evidence of obvious mechanical obstruction. Posterior teeth are preferentially affected (typically with involvement of all teeth distal to the most mesial non-erupted tooth), resulting in a posterior open bite. Non-ankylosed teeth tend to become ankylosed, and orthodontic treatment of affected teeth is generally unsuccessful. |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Some |
2 |
Infraocclusion of tooth due to and following dental trauma (disorder) |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Some |
4 |
Disorder of eruption of permanent tooth due to and following dental trauma (disorder) |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Some |
4 |
Plain X-ray of soft tissue abnormal (finding) |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Some |
1 |
Plain X-ray of toe abnormal |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Some |
1 |
Plain X-ray of finger abnormal (finding) |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Some |
1 |
Plain X-ray of thumb abnormal (finding) |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Some |
1 |
Plain X-ray of fibula abnormal |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Some |
1 |
Plain X-ray of tibia abnormal (finding) |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Some |
1 |
Plain X-ray of lower leg abnormal (finding) |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Some |
1 |
Plain X-ray of bone of lower leg abnormal (finding) |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Some |
1 |
Misophonia (disorder) |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Some |
2 |
Plain X-ray of humerus and bone of shoulder girdle abnormal (finding) |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Some |
1 |
Plain X-ray of radius and ulna abnormal |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Some |
1 |
Plain X-ray of forearm abnormal |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Some |
1 |
Plain X-ray of lower limb abnormal (finding) |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Some |
1 |
Plain X-ray of lumbar and sacral spine abnormal |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Some |
1 |
Plain X-ray of sacral spine abnormal |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Some |
1 |
Plain X-ray of oral soft tissue abnormal |
Has interpretation |
True |
Abnormal |
Inferred relationship |
Some |
1 |