| Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
| Laterality sequence |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Posterior open bite |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| chondrodysplasie métaphysaire type Jansen (trouble) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Glucose-6-phosphate dehydrogenase deficiency class III variant anemia (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
4 |
| syndrome associant rétinite pigmentaire et surdité |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
| Retinitis pigmentosa-deafness-ataxia syndrome |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
| Goldenhar syndrome |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Gorlin-Chaudhry-Moss syndrome |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Oculo-palato-digital syndrome |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Oculo-palato-digital syndrome |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
| Usher syndrome type 1 |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
| Usher syndrome type 2 |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
| Thoracopagus parasiticus |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Hypogonadism, diabetes mellitus, alopecia, mental retardation and electrocardiographic abnormalities (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Megaloblastic anemia, thiamine-responsive, with diabetes mellitus and sensorineural deafness |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
4 |
| Megaloblastic anemia, thiamine-responsive, with diabetes mellitus and sensorineural deafness |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
5 |
| dysplasie oculo-dento-osseuse |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| dysplasie oculo-dento-osseuse |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
3 |
| Floating-Harbour syndrome |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| syndrome de Kabuki |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| syndrome rein-colobome |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| syndrome rein-colobome |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
| Solitary median maxillary central incisor syndrome |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
| Solitary median maxillary central incisor syndrome |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
3 |
| Townes syndrome |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Infantile cortical hyperostosis |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| 7p partial monosomy (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Congenital absence of broad ligament |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Potter's facies |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Congenital postural lordosis |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Congenital cerebral arteriovenous aneurysm |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Congenital anomaly of sternocleidomastoid muscle |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Mild hereditary spherocytosis due to combined deficiency of spectrin AND ankyrin |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Benign adult cystinosis |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Lymphopenic agammaglobulinemia - short-limbed dwarfism syndrome |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| hydroméningocèle (trouble) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Congenital absence of uvula |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Hereditary nonspherocytic hemolytic anemia due to gamma glutamyl cysteine synthetase deficiency (disorder) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Coalition of calcaneus |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Hereditary spherocytosis due to spectrin deficiency |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Longitudinal deficiency of phalanges of foot |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Uterus parvicollis |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Congenital absence of vena cava |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| HSMN IV |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
5 |
| anomalie de l'aqueduc du cerveau |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Primordial cyst |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Autosomal recessive glutaric aciduria, type 2 |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
1 |
| X chromosome-linked pyridoxine responsive sideroblastic anemia |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Congenital absence of left pulmonary artery |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Syndactyly of fingers with fusion of bones |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Ehlers-Danlos syndrome, hydroxylysine-deficient |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Congenital duodenal obstruction due to malrotation of intestine |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Congenital fissure of sternum |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Isolated cystinuria |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Hyperhydroxyprolinemia |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Neonatal iminoglycinuria |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Xeroderma pigmentosum, group C |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| syndrome de Kearns-Sayre (trouble) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Chiari's network |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Congenital atresia of ileum |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| syndrome de Dubowitz |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Congenital absence of rectum |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Bone island |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Maroteaux-Lamy syndrome, intermediate form |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Congenital absence of external auditory canal |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Microcornea |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| déficit en 5-oxoprolinase (trouble) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| transposition totale des gros vaisseaux |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Ectopic bone tissue, congenital |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| atrésie congénitale de l'œsophage (trouble) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Frog fetus |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| tunnel aorto-ventriculaire gauche (trouble) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Senter syndrome |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Chronic granulomatous disease, type IIA |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Uterus incudiformis |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Congenital obstruction of small intestine |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| albinisme oculo-cutané type 2 (trouble) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| syndrome de François |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
2 |
| albinisme oculaire (trouble) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Congenital tracheocele |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| anémie dysérythropoïétique congénitale type III (trouble) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
5 |
| Agyria |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Cat eye syndrome |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| 11p partial trisomy syndrome |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Faun tail syndrome |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
4 |
| ectropion congénital (trouble) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| syringobulbie (trouble) |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Congenital absence of part of brain |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| anodontie |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| syndrome de Robinson avec dystrophie unguéale et surdité |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Persistent thyroglossal duct |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Mucopolysaccharidosis type I-H/S (disorder) |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Coarctation of pulmonary artery |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Peroxisome biogenesis disorder |
survenue (attribut) |
True |
congénital |
Inferred relationship |
Some |
1 |
| Congenital absence of superior vena cava |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Cervical auricle |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Dominant dystrophic epidermolysis bullosa with absence of skin |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Coronary ostium stenosis |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Anterior crossbite |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Autosomal recessive hypohidrotic ectodermal dysplasia syndrome |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|
| Tarsal coalitions |
survenue (attribut) |
False |
congénital |
Inferred relationship |
Some |
|