Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Thromboxane generation defect |
a pour interprétation (attribut) |
True |
anormal |
Inferred relationship |
Some |
1 |
Pigmented purpuric lichenoid dermatitis of Gougerot and Blum |
a pour interprétation (attribut) |
True |
anormal |
Inferred relationship |
Some |
1 |
Hereditary von Willebrand disease type 2B |
a pour interprétation (attribut) |
True |
anormal |
Inferred relationship |
Some |
1 |
DK phocomelia syndrome (disorder) |
a pour interprétation (attribut) |
False |
anormal |
Inferred relationship |
Some |
2 |
thrombocytopénie amégacaryocytique avec malformation congénitale |
a pour interprétation (attribut) |
True |
anormal |
Inferred relationship |
Some |
3 |
Hereditary factor V deficiency disease |
a pour interprétation (attribut) |
True |
anormal |
Inferred relationship |
Some |
1 |
Anti-factor II disorder |
a pour interprétation (attribut) |
True |
anormal |
Inferred relationship |
Some |
1 |
Anticoagulant excess without bleeding |
a pour interprétation (attribut) |
True |
anormal |
Inferred relationship |
Some |
1 |
Elective mutism |
a pour interprétation (attribut) |
False |
anormal |
Inferred relationship |
Some |
1 |
von Willebrand disease type IA |
a pour interprétation (attribut) |
True |
anormal |
Inferred relationship |
Some |
1 |
Radial aplasia-thrombocytopenia syndrome |
a pour interprétation (attribut) |
True |
anormal |
Inferred relationship |
Some |
2 |
Factor XIII deficiency disease |
a pour interprétation (attribut) |
True |
anormal |
Inferred relationship |
Some |
1 |
Blood coagulation disorder due to liver disease |
a pour interprétation (attribut) |
True |
anormal |
Inferred relationship |
Some |
1 |
Severe hereditary factor IX deficiency disease with inhibitor (disorder) |
a pour interprétation (attribut) |
True |
anormal |
Inferred relationship |
Some |
1 |
Haemorrhagic disorder due to antithrombinaemia |
a pour interprétation (attribut) |
True |
anormal |
Inferred relationship |
Some |
1 |
Alpha chain defect dysfibrinogenemia |
a pour interprétation (attribut) |
True |
anormal |
Inferred relationship |
Some |
1 |
Adductor spastic dysphonia of musculoskeletal tension reaction |
a pour interprétation (attribut) |
True |
anormal |
Inferred relationship |
Some |
1 |
Familial multiple factor deficiency syndrome, type III |
a pour interprétation (attribut) |
True |
anormal |
Inferred relationship |
Some |
1 |
Receptive language disorder |
a pour interprétation (attribut) |
True |
anormal |
Inferred relationship |
Some |
1 |
Hyperkinetic aphonia |
a pour interprétation (attribut) |
True |
anormal |
Inferred relationship |
Some |
1 |
Conversion aphonia |
a pour interprétation (attribut) |
True |
anormal |
Inferred relationship |
Some |
1 |
Upshaw-Schulman syndrome (disorder) |
a pour interprétation (attribut) |
False |
anormal |
Inferred relationship |
Some |
8 |
purpura thrombopénique congénital |
a pour interprétation (attribut) |
True |
anormal |
Inferred relationship |
Some |
3 |
von Willebrand disease type IB |
a pour interprétation (attribut) |
True |
anormal |
Inferred relationship |
Some |
1 |
Factor II deficiency |
a pour interprétation (attribut) |
True |
anormal |
Inferred relationship |
Some |
1 |
Mild developmental articulation disorder |
a pour interprétation (attribut) |
True |
anormal |
Inferred relationship |
Some |
1 |
Ataxic dysphonia |
a pour interprétation (attribut) |
True |
anormal |
Inferred relationship |
Some |
1 |
Conversion dysphonia |
a pour interprétation (attribut) |
True |
anormal |
Inferred relationship |
Some |
1 |
Contact purpura (disorder) |
a pour interprétation (attribut) |
True |
anormal |
Inferred relationship |
Some |
2 |
Severe receptive language delay |
a pour interprétation (attribut) |
True |
anormal |
Inferred relationship |
Some |
1 |
Homozygous protein C deficiency (disorder) |
a pour interprétation (attribut) |
True |
anormal |
Inferred relationship |
Some |
1 |
Speech and language disorder |
a pour interprétation (attribut) |
True |
anormal |
Inferred relationship |
Some |
1 |
Sex-linked thrombocytopenia |
a pour interprétation (attribut) |
True |
anormal |
Inferred relationship |
Some |
2 |
Phonological disorder |
a pour interprétation (attribut) |
True |
anormal |
Inferred relationship |
Some |
1 |
Revesz syndrome (disorder) |
a pour interprétation (attribut) |
False |
anormal |
Inferred relationship |
Some |
8 |
Mild hereditary factor VIII deficiency disease without inhibitor (disorder) |
a pour interprétation (attribut) |
True |
anormal |
Inferred relationship |
Some |
1 |
maladie de von Willebrand |
a pour interprétation (attribut) |
True |
anormal |
Inferred relationship |
Some |
1 |
Megakaryocytic thrombocytopenia |
a pour interprétation (attribut) |
True |
anormal |
Inferred relationship |
Some |
2 |
Purpura pigmentosa chronica |
a pour interprétation (attribut) |
True |
anormal |
Inferred relationship |
Some |
2 |
Acute haemorrhagic oedema of childhood |
a pour interprétation (attribut) |
False |
anormal |
Inferred relationship |
Some |
3 |
Dysfluency |
a pour interprétation (attribut) |
True |
anormal |
Inferred relationship |
Some |
1 |
Semantic-pragmatic impairment |
a pour interprétation (attribut) |
True |
anormal |
Inferred relationship |
Some |
1 |
Clothing purpura (disorder) |
a pour interprétation (attribut) |
True |
anormal |
Inferred relationship |
Some |
2 |
von Willebrand disease, type IIH |
a pour interprétation (attribut) |
True |
anormal |
Inferred relationship |
Some |
1 |
Legal termination of pregnancy with afibrinogenemia |
a pour interprétation (attribut) |
False |
anormal |
Inferred relationship |
Some |
1 |
Developmental verbal dyspraxia |
a pour interprétation (attribut) |
True |
anormal |
Inferred relationship |
Some |
1 |
MYH9 macrothrombocytopenia syndrome (disorder) |
a pour interprétation (attribut) |
False |
anormal |
Inferred relationship |
Some |
1 |
Secondary cutaneous vasculitis |
a pour interprétation (attribut) |
True |
anormal |
Inferred relationship |
Some |
3 |
afibrinogénémie |
a pour interprétation (attribut) |
True |
anormal |
Inferred relationship |
Some |
1 |
Heterozygous protein C deficiency (disorder) |
a pour interprétation (attribut) |
True |
anormal |
Inferred relationship |
Some |
1 |
Thrombocytopenic purpura due to platelet consumption (disorder) |
a pour interprétation (attribut) |
True |
anormal |
Inferred relationship |
Some |
3 |
Severe hereditary factor IX deficiency disease without inhibitor (disorder) |
a pour interprétation (attribut) |
True |
anormal |
Inferred relationship |
Some |
1 |
thrombocythémie essentielle |
a pour interprétation (attribut) |
False |
anormal |
Inferred relationship |
Some |
2 |
Refractory thrombocytopenia (disorder) |
a pour interprétation (attribut) |
True |
anormal |
Inferred relationship |
Some |
3 |
Hereditary hyperhomocysteinemia (disorder) |
a pour interprétation (attribut) |
True |
anormal |
Inferred relationship |
Some |
1 |
Hereditary factor XIII B subunit deficiency (disorder) |
a pour interprétation (attribut) |
True |
anormal |
Inferred relationship |
Some |
1 |
Hereditary coagulation factor deficiency |
a pour interprétation (attribut) |
True |
anormal |
Inferred relationship |
Some |
1 |
Transient neonatal thrombocytopenia due to isoimmunisation |
a pour interprétation (attribut) |
True |
anormal |
Inferred relationship |
Some |
2 |
Vitamin K deficiency coagulation disorder |
a pour interprétation (attribut) |
True |
anormal |
Inferred relationship |
Some |
1 |
thrombophilie |
a pour interprétation (attribut) |
True |
anormal |
Inferred relationship |
Some |
1 |
Reactive thrombocytosis |
a pour interprétation (attribut) |
True |
anormal |
Inferred relationship |
Some |
2 |
Homozygous Factor V Leiden mutation |
a pour interprétation (attribut) |
True |
anormal |
Inferred relationship |
Some |
1 |
Neonatal thrombocytopenia due to idiopathic maternal thrombocytopenia |
a pour interprétation (attribut) |
True |
anormal |
Inferred relationship |
Some |
2 |
Coagulation factor deficiency syndrome |
a pour interprétation (attribut) |
True |
anormal |
Inferred relationship |
Some |
1 |
Hypernasality and hyponasality |
a pour interprétation (attribut) |
True |
anormal |
Inferred relationship |
Some |
1 |
High bone mass osteogenesis imperfecta |
a pour interprétation (attribut) |
True |
anormal |
Inferred relationship |
Some |
2 |
Hermansky-Pudlak syndrome |
a pour interprétation (attribut) |
False |
anormal |
Inferred relationship |
Some |
3 |
Osteogenesis imperfecta type I (disorder) |
a pour interprétation (attribut) |
True |
anormal |
Inferred relationship |
Some |
2 |
Ehlers-Danlos and osteogenesis imperfecta syndrome |
a pour interprétation (attribut) |
True |
anormal |
Inferred relationship |
Some |
3 |
Osteogenesis imperfecta type III (disorder) |
a pour interprétation (attribut) |
True |
anormal |
Inferred relationship |
Some |
2 |
Osteogenesis imperfecta type IIA |
a pour interprétation (attribut) |
True |
anormal |
Inferred relationship |
Some |
2 |
Osteogenesis imperfecta, perinatal lethal |
a pour interprétation (attribut) |
True |
anormal |
Inferred relationship |
Some |
2 |
Osteogenesis imperfecta with blue sclerae AND dentinogenesis imperfecta |
a pour interprétation (attribut) |
True |
anormal |
Inferred relationship |
Some |
4 |
Osteogenesis imperfecta type IIB |
a pour interprétation (attribut) |
True |
anormal |
Inferred relationship |
Some |
2 |
Osteogenesis imperfecta |
a pour interprétation (attribut) |
True |
anormal |
Inferred relationship |
Some |
2 |
Osteogenesis imperfecta, type IV B |
a pour interprétation (attribut) |
True |
anormal |
Inferred relationship |
Some |
2 |
Osteogenesis imperfecta with normal sclerae, dominant form |
a pour interprétation (attribut) |
True |
anormal |
Inferred relationship |
Some |
2 |
Osteoporosis with pseudoglioma |
a pour interprétation (attribut) |
True |
anormal |
Inferred relationship |
Some |
2 |
Osteogenesis imperfecta, retinopathy, seizures, intellectual disability syndrome (disorder) |
a pour interprétation (attribut) |
True |
anormal |
Inferred relationship |
Some |
4 |
Osteogenesis imperfecta, type IV A |
a pour interprétation (attribut) |
True |
anormal |
Inferred relationship |
Some |
2 |
Osteogenesis imperfecta, recessive perinatal lethal |
a pour interprétation (attribut) |
True |
anormal |
Inferred relationship |
Some |
2 |
Osteogenesis imperfecta with blue sclerae AND normal teeth |
a pour interprétation (attribut) |
True |
anormal |
Inferred relationship |
Some |
3 |
Osteogenesis imperfecta, dominant perinatal lethal |
a pour interprétation (attribut) |
True |
anormal |
Inferred relationship |
Some |
2 |
Ichthyosis, short stature, brachydactyly, microspherophakia syndrome |
a pour interprétation (attribut) |
True |
anormal |
Inferred relationship |
Some |
5 |
Hereditary hyperekplexia (disorder) |
a pour interprétation (attribut) |
True |
anormal |
Inferred relationship |
Some |
3 |
Sporadic hyperekplexia (disorder) |
a pour interprétation (attribut) |
True |
anormal |
Inferred relationship |
Some |
1 |
Irregular tear film (finding) |
a pour interprétation (attribut) |
True |
anormal |
Inferred relationship |
Some |
1 |
Abnormal hair finding (finding) |
a pour interprétation (attribut) |
True |
anormal |
Inferred relationship |
Some |
1 |
Sexual dysfunction caused by amfetamine and/or amfetamine derivative (finding) |
a pour interprétation (attribut) |
True |
anormal |
Inferred relationship |
Some |
1 |
Acquired hemophilia |
a pour interprétation (attribut) |
True |
anormal |
Inferred relationship |
Some |
1 |
Palmoplantar keratoderma, spastic paralysis syndrome (disorder) |
a pour interprétation (attribut) |
True |
anormal |
Inferred relationship |
Some |
2 |
Hyperekplexia epilepsy syndrome (disorder) |
a pour interprétation (attribut) |
True |
anormal |
Inferred relationship |
Some |
1 |
Chronic instability of bilateral knee joints |
a pour interprétation (attribut) |
False |
anormal |
Inferred relationship |
Some |
2 |
Chronic instability of bilateral knee joints |
a pour interprétation (attribut) |
True |
anormal |
Inferred relationship |
Some |
1 |
Adult onset fluency disorder |
a pour interprétation (attribut) |
True |
anormal |
Inferred relationship |
Some |
1 |
anémie aplasique médicamenteuse |
a pour interprétation (attribut) |
True |
anormal |
Inferred relationship |
Some |
8 |
Acquired factor V deficiency disease |
a pour interprétation (attribut) |
True |
anormal |
Inferred relationship |
Some |
2 |
Systemic lupus erythematosus-associated antiphospholipid syndrome (disorder) |
a pour interprétation (attribut) |
True |
anormal |
Inferred relationship |
Some |
3 |
Perinatal purpura |
a pour interprétation (attribut) |
False |
anormal |
Inferred relationship |
Some |
3 |
Heparin-induced thrombocytopenia |
a pour interprétation (attribut) |
True |
anormal |
Inferred relationship |
Some |
3 |
Bleeding diathesis due to thromboxane synthesis deficiency |
a pour interprétation (attribut) |
True |
anormal |
Inferred relationship |
Some |
4 |