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 |
|