| 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 |